Oligodendroglioma pathophysiology: Difference between revisions

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==Overview==
==Overview==
[[Oligodendroglioma]] arises from the tripotential [[Glial cell|glial precursor cells]] and ''not'' from the [[bipotential]] [[Oligodendrocyte|oligodendrocytes]]. [[Genes]] [[Association (statistics)|associated]] with the [[pathogenesis]] of [[oligodendroglioma]] include [[Translocation|t[1;19][q10;p10]]], [[ATRX]], ''[[Mutation|NJDS]]'', ''[[Isocitrate dehydrogenase|IDH1]]'', ''[[IDH2]]'', [[TERT]] [[promoter]], [[H3F3A|H3]] K27M (''[[H3F3A]], [[HIST1H3B]]/[[HIST1H3C|C]]),'' ''[[CIC (gene)|CIC]]'', ''[[Far upstream element-binding protein 1|FUBP1]]'', ''[[p53]]'', ''[[CD57|Leu-7]]'', ''[[TCF12|TCF-12]]'', ''[[TP53]],[[Ogt|MGMT]]'', ''[[P73|TP73]]'', [[BRAF]], ''[[EGFR]]'', and ''[[PTEN]]''. Common intracranial sites involved by [[oligodendroglioma]] include [[Cerebral hemisphere|cerebral hemispheres]], [[posterior fossa]], and [[Spinal cord|intramedullary spinal cord]]. On [[gross pathology]], [[oligodendroglioma]] is characterized by a well-circumscribed, gelatinous, [[Calcified lesion|calcified]], [[cystic]], [[gray]] [[mass]] with focal [[hemorrhage]] which may expand a [[gyrus]] and remodel the [[skull]]. On [[microscopic]] [[histopathological]] [[analysis]], [[oligodendroglioma]] is characterized by [[diffuse]] [[growth]][[pattern]] of highly [[cellular]] [[lesion]] of monomorphic [[Cells (biology)|cells]] having rounded [[nucleus]] with [[atypia]], speckled "''salt-and-pepper''" [[chromatin]] [[pattern]] and [[Perinuclear space|perinuclear]] [[Halo (medicine)|halo]]<nowiki/>resembling ''fried eggs'', [[Distinctive feature|distinct]] [[Cell (biology)|cell]] borders, clear [[cytoplasm]], abundant [[calcification]] and "''chicken-wire''" like [[vascularity]] [[pattern]]. [[Oligodendroglioma]] is demonstrated by [[Positivity effect|positivity]] to [[tumor markers]] such as [[Isocitrate dehydrogenase|IDH1-R132H]], [[Microtubule-associated protein|MAP2]], [[GFAP]], [[S100 calcium binding protein A8|S-100]], [[SOX10]], EMA, [[ATRX]], [[Ki-67 (Biology)|Ki-67]], [[Neuron-Specific Enolase (NSE)|NSE]], [[synaptophysin]], [[OLIG1]], and [[OLIG2]].
[[Oligodendroglioma]] arises from the tripotential [[Glial cell|glial precursor cells]] and ''not'' from the [[bipotential]] [[Oligodendrocyte|oligodendrocytes]]. [[Genes]] [[Association (statistics)|associated]] with the [[pathogenesis]] of [[oligodendroglioma]] include [[Translocation|t[1;19][q10;p10]]], [[ATRX]], ''[[Mutation|NJDS]]'', ''[[Isocitrate dehydrogenase|IDH1]]'', ''[[IDH2]]'', [[TERT]] [[promoter]], [[H3F3A|H3]] K27M (''[[H3F3A]], [[HIST1H3B]]/[[HIST1H3C|C]]),'' ''[[CIC (gene)|CIC]]'', ''[[Far upstream element-binding protein 1|FUBP1]]'', ''[[p53]]'', ''[[CD57|Leu-7]]'', ''[[TCF12|TCF-12]]'', ''[[TP53]],[[Ogt|MGMT]]'', ''[[P73|TP73]]'', [[BRAF]], ''[[EGFR]]'', and ''[[PTEN]]''. Common intracranial sites involved by [[oligodendroglioma]] include [[Cerebral hemisphere|cerebral hemispheres]], [[posterior fossa]], and [[Spinal cord|intramedullary spinal cord]]. On [[gross pathology]], [[oligodendroglioma]] is characterized by a well-circumscribed, gelatinous, [[Calcified lesion|calcified]], [[cystic]], [[gray]] [[mass]] with focal [[hemorrhage]] which may expand a [[gyrus]] and remodel the [[skull]]. On [[microscopic]] [[histopathological]] [[analysis]], [[oligodendroglioma]] is characterized by [[diffuse]] [[growth]][[pattern]] of highly [[cellular]] [[lesion]] of monomorphic [[Cells (biology)|cells]] having rounded [[nucleus]] with [[atypia]], speckled "''[[salt]]-and-[[Pepper spray|pepper]]''" [[chromatin]] [[pattern]] and [[Perinuclear space|perinuclear]] [[Halo (medicine)|halo]]<nowiki/>resembling ''fried [[Egg (biology)|eggs]]'', [[Distinctive feature|distinct]] [[Cell (biology)|cell]] borders, clear [[cytoplasm]], abundant [[calcification]] and "''chicken-wire''" like [[vascularity]] [[pattern]]. [[Oligodendroglioma]] is demonstrated by [[Positivity effect|positivity]] to [[tumor markers]] such as [[Isocitrate dehydrogenase|IDH1-R132H]], [[Microtubule-associated protein|MAP2]], [[GFAP]], [[S100 calcium binding protein A8|S-100]], [[SOX10]], EMA, [[ATRX]], [[Ki-67 (Biology)|Ki-67]], [[Neuron-Specific Enolase (NSE)|NSE]], [[synaptophysin]], [[OLIG1]], and [[OLIG2]].


==Pathophysiology==
==Pathophysiology==
===Pathogenesis===
===Pathogenesis===
*[[Oligodendroglioma]] does ''not'' arise from the [[bipotential]] [[oligodendrocyte]]s, although the [[tumor]] [[Cells (biology)|cells]] look very similiar<ref name="pathogenesis">General features of oligodendroglioma. Libre Pathology. http://librepathology.org/wiki/index.php/Oligodendroglioma#cite_note-1</ref>
*[[Oligodendroglioma]] does ''not'' arise from the [[bipotential]] [[oligodendrocyte]]s, although the [[tumor]] [[Cells (biology)|cells]] look very similiar.<ref name="pathogenesis">General features of oligodendroglioma. Libre Pathology. http://librepathology.org/wiki/index.php/Oligodendroglioma#cite_note-1</ref>
*[[Oligodendroglioma]] arises from the tripotential [[glial cell|glial precursor cells]]
*[[Oligodendroglioma]] arises from the tripotential [[glial cell|glial precursor cells]].


===Genetics===
===Genetics===
*[[Development]] of [[oligodendroglioma]] is the [[result]] of multiple [[mutation|genetic mutations]]<ref name="pmid25848751">{{cite journal| author=Suzuki H, Aoki K, Chiba K, Sato Y, Shiozawa Y, Shiraishi Y et al.| title=Mutational landscape and clonal architecture in grade II and III gliomas. | journal=Nat Genet | year= 2015 | volume= 47 | issue= 5 | pages= 458-68 | pmid=25848751 | doi=10.1038/ng.3273 | pmc= | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=25848751  }} </ref><ref name="pmid26210286">{{cite journal| author=Leeper HE, Caron AA, Decker PA, Jenkins RB, Lachance DH, Giannini C| title=IDH mutation, 1p19q codeletion and ATRX loss in WHO grade II gliomas. | journal=Oncotarget | year= 2015 | volume= 6 | issue= 30 | pages= 30295-305 | pmid=26210286 | doi=10.18632/oncotarget.4497 | pmc=4745799 | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=26210286  }} </ref><ref name="pmid24470545">{{cite journal| author=Sabha N, Knobbe CB, Maganti M, Al Omar S, Bernstein M, Cairns R et al.| title=Analysis of IDH mutation, 1p/19q deletion, and PTEN loss delineates prognosis in clinical low-grade diffuse gliomas. | journal=Neuro Oncol | year= 2014 | volume= 16 | issue= 7 | pages= 914-23 | pmid=24470545 | doi=10.1093/neuonc/not299 | pmc=4057130 | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=24470545  }} </ref><ref name="pmid23583981">{{cite journal| author=Zhang J, Wu G, Miller CP, Tatevossian RG, Dalton JD, Tang B et al.| title=Whole-genome sequencing identifies genetic alterations in pediatric low-grade gliomas. | journal=Nat Genet | year= 2013 | volume= 45 | issue= 6 | pages= 602-12 | pmid=23583981 | doi=10.1038/ng.2611 | pmc=3727232 | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=23583981  }} </ref><ref name="pmid24705251">{{cite journal| author=Wu G, Diaz AK, Paugh BS, Rankin SL, Ju B, Li Y et al.| title=The genomic landscape of diffuse intrinsic pontine glioma and pediatric non-brainstem high-grade glioma. | journal=Nat Genet | year= 2014 | volume= 46 | issue= 5 | pages= 444-450 | pmid=24705251 | doi=10.1038/ng.2938 | pmc=4056452 | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=24705251  }} </ref><ref name="pmid26671986">{{cite journal| author=Tanboon J, Williams EA, Louis DN| title=The Diagnostic Use of Immunohistochemical Surrogates for Signature Molecular Genetic Alterations in Gliomas. | journal=J Neuropathol Exp Neurol | year= 2016 | volume= 75 | issue= 1 | pages= 4-18 | pmid=26671986 | doi=10.1093/jnen/nlv009 | pmc= | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=26671986  }} </ref><ref name="pmid22869205">{{cite journal| author=Jiao Y, Killela PJ, Reitman ZJ, Rasheed AB, Heaphy CM, de Wilde RF et al.| title=Frequent ATRX, CIC, FUBP1 and IDH1 mutations refine the classification of malignant gliomas. | journal=Oncotarget | year= 2012 | volume= 3 | issue= 7 | pages= 709-22 | pmid=22869205 | doi=10.18632/oncotarget.588 | pmc=3443254 | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=22869205  }} </ref><ref name="pmid22588899">{{cite journal| author=Sahm F, Koelsche C, Meyer J, Pusch S, Lindenberg K, Mueller W et al.| title=CIC and FUBP1 mutations in oligodendrogliomas, oligoastrocytomas and astrocytomas. | journal=Acta Neuropathol | year= 2012 | volume= 123 | issue= 6 | pages= 853-60 | pmid=22588899 | doi=10.1007/s00401-012-0993-5 | pmc= | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=22588899  }} </ref><ref name="pmid15709179">{{cite journal| author=Barbashina V, Salazar P, Holland EC, Rosenblum MK, Ladanyi M| title=Allelic losses at 1p36 and 19q13 in gliomas: correlation with histologic classification, definition of a 150-kb minimal deleted region on 1p36, and evaluation of CAMTA1 as a candidate tumor suppressor gene. | journal=Clin Cancer Res | year= 2005 | volume= 11 | issue= 3 | pages= 1119-28 | pmid=15709179 | doi= | pmc= | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=15709179  }} </ref><ref name="pmid23681562">{{cite journal| author=Frenel JS, Leux C, Loussouarn D, Le Loupp AG, Leclair F, Aumont M et al.| title=Combining two biomarkers, IDH1/2 mutations and 1p/19q codeletion, to stratify anaplastic oligodendroglioma in three groups: a single-center experience. | journal=J Neurooncol | year= 2013 | volume= 114 | issue= 1 | pages= 85-91 | pmid=23681562 | doi=10.1007/s11060-013-1152-0 | pmc= | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=23681562  }} </ref><ref name="pmid27651340">{{cite journal| author=Hacisalihoglu P, Kucukodaci Z, Gundogdu G, Bilgic B| title=The Correlation Between 1p/19q Codeletion, IDH1 Mutation, p53 Overexpression and Their Prognostic Roles in 41 Turkish Anaplastic Oligodendroglioma Patients. | journal=Turk Neurosurg | year= 2017 | volume= 27 | issue= 5 | pages= 682-689 | pmid=27651340 | doi=10.5137/1019-5149.JTN.16832-15.1 | pmc= | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=27651340  }} </ref>
*[[Development]] of [[oligodendroglioma]] is the [[result]] of multiple [[mutation|genetic mutations.]]<ref name="pmid25848751">{{cite journal| author=Suzuki H, Aoki K, Chiba K, Sato Y, Shiozawa Y, Shiraishi Y et al.| title=Mutational landscape and clonal architecture in grade II and III gliomas. | journal=Nat Genet | year= 2015 | volume= 47 | issue= 5 | pages= 458-68 | pmid=25848751 | doi=10.1038/ng.3273 | pmc= | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=25848751  }} </ref><ref name="pmid26210286">{{cite journal| author=Leeper HE, Caron AA, Decker PA, Jenkins RB, Lachance DH, Giannini C| title=IDH mutation, 1p19q codeletion and ATRX loss in WHO grade II gliomas. | journal=Oncotarget | year= 2015 | volume= 6 | issue= 30 | pages= 30295-305 | pmid=26210286 | doi=10.18632/oncotarget.4497 | pmc=4745799 | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=26210286  }} </ref><ref name="pmid24470545">{{cite journal| author=Sabha N, Knobbe CB, Maganti M, Al Omar S, Bernstein M, Cairns R et al.| title=Analysis of IDH mutation, 1p/19q deletion, and PTEN loss delineates prognosis in clinical low-grade diffuse gliomas. | journal=Neuro Oncol | year= 2014 | volume= 16 | issue= 7 | pages= 914-23 | pmid=24470545 | doi=10.1093/neuonc/not299 | pmc=4057130 | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=24470545  }} </ref><ref name="pmid23583981">{{cite journal| author=Zhang J, Wu G, Miller CP, Tatevossian RG, Dalton JD, Tang B et al.| title=Whole-genome sequencing identifies genetic alterations in pediatric low-grade gliomas. | journal=Nat Genet | year= 2013 | volume= 45 | issue= 6 | pages= 602-12 | pmid=23583981 | doi=10.1038/ng.2611 | pmc=3727232 | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=23583981  }} </ref><ref name="pmid24705251">{{cite journal| author=Wu G, Diaz AK, Paugh BS, Rankin SL, Ju B, Li Y et al.| title=The genomic landscape of diffuse intrinsic pontine glioma and pediatric non-brainstem high-grade glioma. | journal=Nat Genet | year= 2014 | volume= 46 | issue= 5 | pages= 444-450 | pmid=24705251 | doi=10.1038/ng.2938 | pmc=4056452 | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=24705251  }} </ref><ref name="pmid26671986">{{cite journal| author=Tanboon J, Williams EA, Louis DN| title=The Diagnostic Use of Immunohistochemical Surrogates for Signature Molecular Genetic Alterations in Gliomas. | journal=J Neuropathol Exp Neurol | year= 2016 | volume= 75 | issue= 1 | pages= 4-18 | pmid=26671986 | doi=10.1093/jnen/nlv009 | pmc= | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=26671986  }} </ref><ref name="pmid22869205">{{cite journal| author=Jiao Y, Killela PJ, Reitman ZJ, Rasheed AB, Heaphy CM, de Wilde RF et al.| title=Frequent ATRX, CIC, FUBP1 and IDH1 mutations refine the classification of malignant gliomas. | journal=Oncotarget | year= 2012 | volume= 3 | issue= 7 | pages= 709-22 | pmid=22869205 | doi=10.18632/oncotarget.588 | pmc=3443254 | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=22869205  }} </ref><ref name="pmid22588899">{{cite journal| author=Sahm F, Koelsche C, Meyer J, Pusch S, Lindenberg K, Mueller W et al.| title=CIC and FUBP1 mutations in oligodendrogliomas, oligoastrocytomas and astrocytomas. | journal=Acta Neuropathol | year= 2012 | volume= 123 | issue= 6 | pages= 853-60 | pmid=22588899 | doi=10.1007/s00401-012-0993-5 | pmc= | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=22588899  }} </ref><ref name="pmid15709179">{{cite journal| author=Barbashina V, Salazar P, Holland EC, Rosenblum MK, Ladanyi M| title=Allelic losses at 1p36 and 19q13 in gliomas: correlation with histologic classification, definition of a 150-kb minimal deleted region on 1p36, and evaluation of CAMTA1 as a candidate tumor suppressor gene. | journal=Clin Cancer Res | year= 2005 | volume= 11 | issue= 3 | pages= 1119-28 | pmid=15709179 | doi= | pmc= | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=15709179  }} </ref><ref name="pmid23681562">{{cite journal| author=Frenel JS, Leux C, Loussouarn D, Le Loupp AG, Leclair F, Aumont M et al.| title=Combining two biomarkers, IDH1/2 mutations and 1p/19q codeletion, to stratify anaplastic oligodendroglioma in three groups: a single-center experience. | journal=J Neurooncol | year= 2013 | volume= 114 | issue= 1 | pages= 85-91 | pmid=23681562 | doi=10.1007/s11060-013-1152-0 | pmc= | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=23681562  }} </ref><ref name="pmid27651340">{{cite journal| author=Hacisalihoglu P, Kucukodaci Z, Gundogdu G, Bilgic B| title=The Correlation Between 1p/19q Codeletion, IDH1 Mutation, p53 Overexpression and Their Prognostic Roles in 41 Turkish Anaplastic Oligodendroglioma Patients. | journal=Turk Neurosurg | year= 2017 | volume= 27 | issue= 5 | pages= 682-689 | pmid=27651340 | doi=10.5137/1019-5149.JTN.16832-15.1 | pmc= | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=27651340  }} </ref>
*[[Genes]] [[Association (statistics)|associated]] with the [[pathogenesis]] of [[oligodendroglioma]] include:<ref name="transloc">Molecular genetics of oligodendroglioma. https://en.wikipedia.org/wiki/Oligodendroglioma</ref><ref name="pmid21817013">{{cite journal| author=Bettegowda C, Agrawal N, Jiao Y, Sausen M, Wood LD, Hruban RH et al.| title=Mutations in CIC and FUBP1 contribute to human oligodendroglioma. | journal=Science | year= 2011 | volume= 333 | issue= 6048 | pages= 1453-5 | pmid=21817013 | doi=10.1126/science.1210557 | pmc=PMC3170506 | url=http://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=21817013  }} </ref><ref name="prog">Prognosis and treatment of oligodendroglioma. Wikipedia 2015. https://en.wikipedia.org/wiki/Oligodendroglioma</ref><ref name="pmid22072542">{{cite journal| author=Yip S, Butterfield YS, Morozova O, Chittaranjan S, Blough MD, An J et al.| title=Concurrent CIC mutations, IDH mutations, and 1p/19q loss distinguish oligodendrogliomas from other cancers. | journal=J Pathol | year= 2012 | volume= 226 | issue= 1 | pages= 7-16 | pmid=22072542 | doi=10.1002/path.2995 | pmc=PMC3246739 | url=http://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=22072542  }} </ref><ref name="pmid26068201">{{cite journal| author=Labreche K, Simeonova I, Kamoun A, Gleize V, Chubb D, Letouzé E et al.| title=TCF12 is mutated in anaplastic oligodendroglioma. | journal=Nat Commun | year= 2015 | volume= 6 | issue=  | pages= 7207 | pmid=26068201 | doi=10.1038/ncomms8207 | pmc=PMC4490400 | url=http://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=26068201  }} </ref><ref name="pmid21937591">{{cite journal| author=Suri V, Jha P, Agarwal S, Pathak P, Sharma MC, Sharma V et al.| title=Molecular profile of oligodendrogliomas in young patients. | journal=Neuro Oncol | year= 2011 | volume= 13 | issue= 10 | pages= 1099-106 | pmid=21937591 | doi=10.1093/neuonc/nor146 | pmc=PMC3177666 | url=http://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=21937591  }} </ref><ref name="pmid9038605">{{cite journal| author=Hagel C, Laking G, Laas R, Scheil S, Jung R, Milde-Langosch K et al.| title=Demonstration of p53 protein and TP53 gene mutations in oligodendrogliomas. | journal=Eur J Cancer | year= 1996 | volume= 32A | issue= 13 | pages= 2242-8 | pmid=9038605 | doi= | pmc= | url=http://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=9038605  }} </ref><ref name="von DeimlingHartmann2005">{{cite journal|last1=von Deimling|first1=A|last2=Hartmann|first2=C|title=Oligodendrogliomas: Impact of molecular genetics on treatment|journal=Neurology India|volume=53|issue=2|year=2005|pages=140|issn=0028-3886|doi=10.4103/0028-3886.16394}}</ref><ref name="pmid26061751">{{cite journal| author=Cancer Genome Atlas Research Network. Brat DJ, Verhaak RG, Aldape KD, Yung WK, Salama SR et al.| title=Comprehensive, Integrative Genomic Analysis of Diffuse Lower-Grade Gliomas. | journal=N Engl J Med | year= 2015 | volume= 372 | issue= 26 | pages= 2481-98 | pmid=26061751 | doi=10.1056/NEJMoa1402121 | pmc=4530011 | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=26061751  }} </ref><ref name="pmid26061753">{{cite journal| author=Eckel-Passow JE, Lachance DH, Molinaro AM, Walsh KM, Decker PA, Sicotte H et al.| title=Glioma Groups Based on 1p/19q, IDH, and TERT Promoter Mutations in Tumors. | journal=N Engl J Med | year= 2015 | volume= 372 | issue= 26 | pages= 2499-508 | pmid=26061753 | doi=10.1056/NEJMoa1407279 | pmc=4489704 | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=26061753  }} </ref><ref name="pmid11801559">{{cite journal| author=Ueki K, Nishikawa R, Nakazato Y, Hirose T, Hirato J, Funada N et al.| title=Correlation of histology and molecular genetic analysis of 1p, 19q, 10q, TP53, EGFR, CDK4, and CDKN2A in 91 astrocytic and oligodendroglial tumors. | journal=Clin Cancer Res | year= 2002 | volume= 8 | issue= 1 | pages= 196-201 | pmid=11801559 | doi= | pmc= | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=11801559  }} </ref><ref name="pmid25150284">{{cite journal| author=Labussière M, Boisselier B, Mokhtari K, Di Stefano AL, Rahimian A, Rossetto M et al.| title=Combined analysis of TERT, EGFR, and IDH status defines distinct prognostic glioblastoma classes. | journal=Neurology | year= 2014 | volume= 83 | issue= 13 | pages= 1200-6 | pmid=25150284 | doi=10.1212/WNL.0000000000000814 | pmc= | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=25150284  }} </ref><ref name="pmid30030640">{{cite journal| author=Nambirajan A, Suri V, Kedia S, Goyal K, Malgulwar PB, Khanna G et al.| title=Paediatric diffuse leptomeningeal tumor with glial and neuronal differentiation harbouring chromosome 1p/19q co-deletion and H3.3 K27M mutation: unusual molecular profile and its therapeutic implications. | journal=Brain Tumor Pathol | year= 2018 | volume= 35 | issue= 3 | pages= 186-191 | pmid=30030640 | doi=10.1007/s10014-018-0325-0 | pmc= | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=30030640  }} </ref>
*[[Genes]] [[Association (statistics)|associated]] with the [[pathogenesis]] of [[oligodendroglioma]] include:<ref name="transloc">Molecular genetics of oligodendroglioma. https://en.wikipedia.org/wiki/Oligodendroglioma</ref><ref name="pmid21817013">{{cite journal| author=Bettegowda C, Agrawal N, Jiao Y, Sausen M, Wood LD, Hruban RH et al.| title=Mutations in CIC and FUBP1 contribute to human oligodendroglioma. | journal=Science | year= 2011 | volume= 333 | issue= 6048 | pages= 1453-5 | pmid=21817013 | doi=10.1126/science.1210557 | pmc=PMC3170506 | url=http://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=21817013  }} </ref><ref name="prog">Prognosis and treatment of oligodendroglioma. Wikipedia 2015. https://en.wikipedia.org/wiki/Oligodendroglioma</ref><ref name="pmid22072542">{{cite journal| author=Yip S, Butterfield YS, Morozova O, Chittaranjan S, Blough MD, An J et al.| title=Concurrent CIC mutations, IDH mutations, and 1p/19q loss distinguish oligodendrogliomas from other cancers. | journal=J Pathol | year= 2012 | volume= 226 | issue= 1 | pages= 7-16 | pmid=22072542 | doi=10.1002/path.2995 | pmc=PMC3246739 | url=http://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=22072542  }} </ref><ref name="pmid26068201">{{cite journal| author=Labreche K, Simeonova I, Kamoun A, Gleize V, Chubb D, Letouzé E et al.| title=TCF12 is mutated in anaplastic oligodendroglioma. | journal=Nat Commun | year= 2015 | volume= 6 | issue=  | pages= 7207 | pmid=26068201 | doi=10.1038/ncomms8207 | pmc=PMC4490400 | url=http://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=26068201  }} </ref><ref name="pmid21937591">{{cite journal| author=Suri V, Jha P, Agarwal S, Pathak P, Sharma MC, Sharma V et al.| title=Molecular profile of oligodendrogliomas in young patients. | journal=Neuro Oncol | year= 2011 | volume= 13 | issue= 10 | pages= 1099-106 | pmid=21937591 | doi=10.1093/neuonc/nor146 | pmc=PMC3177666 | url=http://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=21937591  }} </ref><ref name="pmid9038605">{{cite journal| author=Hagel C, Laking G, Laas R, Scheil S, Jung R, Milde-Langosch K et al.| title=Demonstration of p53 protein and TP53 gene mutations in oligodendrogliomas. | journal=Eur J Cancer | year= 1996 | volume= 32A | issue= 13 | pages= 2242-8 | pmid=9038605 | doi= | pmc= | url=http://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=9038605  }} </ref><ref name="von DeimlingHartmann2005">{{cite journal|last1=von Deimling|first1=A|last2=Hartmann|first2=C|title=Oligodendrogliomas: Impact of molecular genetics on treatment|journal=Neurology India|volume=53|issue=2|year=2005|pages=140|issn=0028-3886|doi=10.4103/0028-3886.16394}}</ref><ref name="pmid26061751">{{cite journal| author=Cancer Genome Atlas Research Network. Brat DJ, Verhaak RG, Aldape KD, Yung WK, Salama SR et al.| title=Comprehensive, Integrative Genomic Analysis of Diffuse Lower-Grade Gliomas. | journal=N Engl J Med | year= 2015 | volume= 372 | issue= 26 | pages= 2481-98 | pmid=26061751 | doi=10.1056/NEJMoa1402121 | pmc=4530011 | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=26061751  }} </ref><ref name="pmid26061753">{{cite journal| author=Eckel-Passow JE, Lachance DH, Molinaro AM, Walsh KM, Decker PA, Sicotte H et al.| title=Glioma Groups Based on 1p/19q, IDH, and TERT Promoter Mutations in Tumors. | journal=N Engl J Med | year= 2015 | volume= 372 | issue= 26 | pages= 2499-508 | pmid=26061753 | doi=10.1056/NEJMoa1407279 | pmc=4489704 | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=26061753  }} </ref><ref name="pmid11801559">{{cite journal| author=Ueki K, Nishikawa R, Nakazato Y, Hirose T, Hirato J, Funada N et al.| title=Correlation of histology and molecular genetic analysis of 1p, 19q, 10q, TP53, EGFR, CDK4, and CDKN2A in 91 astrocytic and oligodendroglial tumors. | journal=Clin Cancer Res | year= 2002 | volume= 8 | issue= 1 | pages= 196-201 | pmid=11801559 | doi= | pmc= | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=11801559  }} </ref><ref name="pmid25150284">{{cite journal| author=Labussière M, Boisselier B, Mokhtari K, Di Stefano AL, Rahimian A, Rossetto M et al.| title=Combined analysis of TERT, EGFR, and IDH status defines distinct prognostic glioblastoma classes. | journal=Neurology | year= 2014 | volume= 83 | issue= 13 | pages= 1200-6 | pmid=25150284 | doi=10.1212/WNL.0000000000000814 | pmc= | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=25150284  }} </ref><ref name="pmid30030640">{{cite journal| author=Nambirajan A, Suri V, Kedia S, Goyal K, Malgulwar PB, Khanna G et al.| title=Paediatric diffuse leptomeningeal tumor with glial and neuronal differentiation harbouring chromosome 1p/19q co-deletion and H3.3 K27M mutation: unusual molecular profile and its therapeutic implications. | journal=Brain Tumor Pathol | year= 2018 | volume= 35 | issue= 3 | pages= 186-191 | pmid=30030640 | doi=10.1007/s10014-018-0325-0 | pmc= | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=30030640  }} </ref>
:*[[translocation|t(1;19)(q10;p10)]] (co-[[Deletion (genetics)|deletion]] of [[chromosomal]] arms [[chromosome 1|1p]]36 and [[chromosome 19|19q]]13; most common)<ref name="pmid16088966">{{cite journal| author=McDonald JM, See SJ, Tremont IW, Colman H, Gilbert MR, Groves M et al.| title=The prognostic impact of histology and 1p/19q status in anaplastic oligodendroglial tumors. | journal=Cancer | year= 2005 | volume= 104 | issue= 7 | pages= 1468-77 | pmid=16088966 | doi=10.1002/cncr.21338 | pmc= | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=16088966  }} </ref><ref name="pmid15709179">{{cite journal| author=Barbashina V, Salazar P, Holland EC, Rosenblum MK, Ladanyi M| title=Allelic losses at 1p36 and 19q13 in gliomas: correlation with histologic classification, definition of a 150-kb minimal deleted region on 1p36, and evaluation of CAMTA1 as a candidate tumor suppressor gene. | journal=Clin Cancer Res | year= 2005 | volume= 11 | issue= 3 | pages= 1119-28 | pmid=15709179 | doi= | pmc= | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=15709179  }} </ref><ref name="pmid7977648">{{cite journal| author=Reifenberger J, Reifenberger G, Liu L, James CD, Wechsler W, Collins VP| title=Molecular genetic analysis of oligodendroglial tumors shows preferential allelic deletions on 19q and 1p. | journal=Am J Pathol | year= 1994 | volume= 145 | issue= 5 | pages= 1175-90 | pmid=7977648 | doi= | pmc=1887413 | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=7977648  }} </ref>
:*[[translocation|t(1;19)(q10;p10)]] (co-[[Deletion (genetics)|deletion]] of [[chromosomal]] arms [[chromosome 1|1p]]36 and [[chromosome 19|19q]]13; most common)<ref name="pmid16088966">{{cite journal| author=McDonald JM, See SJ, Tremont IW, Colman H, Gilbert MR, Groves M et al.| title=The prognostic impact of histology and 1p/19q status in anaplastic oligodendroglial tumors. | journal=Cancer | year= 2005 | volume= 104 | issue= 7 | pages= 1468-77 | pmid=16088966 | doi=10.1002/cncr.21338 | pmc= | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=16088966  }} </ref><ref name="pmid15709179">{{cite journal| author=Barbashina V, Salazar P, Holland EC, Rosenblum MK, Ladanyi M| title=Allelic losses at 1p36 and 19q13 in gliomas: correlation with histologic classification, definition of a 150-kb minimal deleted region on 1p36, and evaluation of CAMTA1 as a candidate tumor suppressor gene. | journal=Clin Cancer Res | year= 2005 | volume= 11 | issue= 3 | pages= 1119-28 | pmid=15709179 | doi= | pmc= | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=15709179  }} </ref><ref name="pmid7977648">{{cite journal| author=Reifenberger J, Reifenberger G, Liu L, James CD, Wechsler W, Collins VP| title=Molecular genetic analysis of oligodendroglial tumors shows preferential allelic deletions on 19q and 1p. | journal=Am J Pathol | year= 1994 | volume= 145 | issue= 5 | pages= 1175-90 | pmid=7977648 | doi= | pmc=1887413 | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=7977648  }} </ref>
Line 19: Line 19:
:*''[[IDH2]]''<ref name="pmid24004584">{{cite journal| author=Pan Y, Qi XL, Wang LM, Dong RF, Zhang M, Zheng DF et al.| title=[Mutation of isocitrate dehydrogenase gene in Chinese patients with glioma]. | journal=Zhonghua Bing Li Xue Za Zhi | year= 2013 | volume= 42 | issue= 5 | pages= 292-8 | pmid=24004584 | doi=10.3760/cma.j.issn.0529-5807.2013.05.002 | pmc= | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=24004584  }} </ref><ref name="pmid19554337">{{cite journal| author=Hartmann C, Meyer J, Balss J, Capper D, Mueller W, Christians A et al.| title=Type and frequency of IDH1 and IDH2 mutations are related to astrocytic and oligodendroglial differentiation and age: a study of 1,010 diffuse gliomas. | journal=Acta Neuropathol | year= 2009 | volume= 118 | issue= 4 | pages= 469-74 | pmid=19554337 | doi=10.1007/s00401-009-0561-9 | pmc= | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=19554337  }} </ref><ref name="pmid19765000">{{cite journal| author=Sonoda Y, Kumabe T, Nakamura T, Saito R, Kanamori M, Yamashita Y et al.| title=Analysis of IDH1 and IDH2 mutations in Japanese glioma patients. | journal=Cancer Sci | year= 2009 | volume= 100 | issue= 10 | pages= 1996-8 | pmid=19765000 | doi=10.1111/j.1349-7006.2009.01270.x | pmc= | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=19765000  }} </ref><ref name="pmid25008158">{{cite journal| author=Arita H, Narita Y, Yoshida A, Hashimoto N, Yoshimine T, Ichimura K| title=IDH1/2 mutation detection in gliomas. | journal=Brain Tumor Pathol | year= 2015 | volume= 32 | issue= 2 | pages= 79-89 | pmid=25008158 | doi=10.1007/s10014-014-0197-x | pmc= | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=25008158  }} </ref><ref name="pmid20160062">{{cite journal| author=van den Bent MJ, Dubbink HJ, Marie Y, Brandes AA, Taphoorn MJ, Wesseling P et al.| title=IDH1 and IDH2 mutations are prognostic but not predictive for outcome in anaplastic oligodendroglial tumors: a report of the European Organization for Research and Treatment of Cancer Brain Tumor Group. | journal=Clin Cancer Res | year= 2010 | volume= 16 | issue= 5 | pages= 1597-604 | pmid=20160062 | doi=10.1158/1078-0432.CCR-09-2902 | pmc= | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=20160062  }} </ref><ref name="pmid24889502">{{cite journal| author=Catteau A, Girardi H, Monville F, Poggionovo C, Carpentier S, Frayssinet V et al.| title=A new sensitive PCR assay for one-step detection of 12 IDH1/2 mutations in glioma. | journal=Acta Neuropathol Commun | year= 2014 | volume= 2 | issue=  | pages= 58 | pmid=24889502 | doi=10.1186/2051-5960-2-58 | pmc=4229941 | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=24889502  }} </ref>
:*''[[IDH2]]''<ref name="pmid24004584">{{cite journal| author=Pan Y, Qi XL, Wang LM, Dong RF, Zhang M, Zheng DF et al.| title=[Mutation of isocitrate dehydrogenase gene in Chinese patients with glioma]. | journal=Zhonghua Bing Li Xue Za Zhi | year= 2013 | volume= 42 | issue= 5 | pages= 292-8 | pmid=24004584 | doi=10.3760/cma.j.issn.0529-5807.2013.05.002 | pmc= | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=24004584  }} </ref><ref name="pmid19554337">{{cite journal| author=Hartmann C, Meyer J, Balss J, Capper D, Mueller W, Christians A et al.| title=Type and frequency of IDH1 and IDH2 mutations are related to astrocytic and oligodendroglial differentiation and age: a study of 1,010 diffuse gliomas. | journal=Acta Neuropathol | year= 2009 | volume= 118 | issue= 4 | pages= 469-74 | pmid=19554337 | doi=10.1007/s00401-009-0561-9 | pmc= | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=19554337  }} </ref><ref name="pmid19765000">{{cite journal| author=Sonoda Y, Kumabe T, Nakamura T, Saito R, Kanamori M, Yamashita Y et al.| title=Analysis of IDH1 and IDH2 mutations in Japanese glioma patients. | journal=Cancer Sci | year= 2009 | volume= 100 | issue= 10 | pages= 1996-8 | pmid=19765000 | doi=10.1111/j.1349-7006.2009.01270.x | pmc= | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=19765000  }} </ref><ref name="pmid25008158">{{cite journal| author=Arita H, Narita Y, Yoshida A, Hashimoto N, Yoshimine T, Ichimura K| title=IDH1/2 mutation detection in gliomas. | journal=Brain Tumor Pathol | year= 2015 | volume= 32 | issue= 2 | pages= 79-89 | pmid=25008158 | doi=10.1007/s10014-014-0197-x | pmc= | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=25008158  }} </ref><ref name="pmid20160062">{{cite journal| author=van den Bent MJ, Dubbink HJ, Marie Y, Brandes AA, Taphoorn MJ, Wesseling P et al.| title=IDH1 and IDH2 mutations are prognostic but not predictive for outcome in anaplastic oligodendroglial tumors: a report of the European Organization for Research and Treatment of Cancer Brain Tumor Group. | journal=Clin Cancer Res | year= 2010 | volume= 16 | issue= 5 | pages= 1597-604 | pmid=20160062 | doi=10.1158/1078-0432.CCR-09-2902 | pmc= | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=20160062  }} </ref><ref name="pmid24889502">{{cite journal| author=Catteau A, Girardi H, Monville F, Poggionovo C, Carpentier S, Frayssinet V et al.| title=A new sensitive PCR assay for one-step detection of 12 IDH1/2 mutations in glioma. | journal=Acta Neuropathol Commun | year= 2014 | volume= 2 | issue=  | pages= 58 | pmid=24889502 | doi=10.1186/2051-5960-2-58 | pmc=4229941 | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=24889502  }} </ref>
:*[[TERT]] [[promoter]]<ref name="pmid26061753">{{cite journal| author=Eckel-Passow JE, Lachance DH, Molinaro AM, Walsh KM, Decker PA, Sicotte H et al.| title=Glioma Groups Based on 1p/19q, IDH, and TERT Promoter Mutations in Tumors. | journal=N Engl J Med | year= 2015 | volume= 372 | issue= 26 | pages= 2499-508 | pmid=26061753 | doi=10.1056/NEJMoa1407279 | pmc=4489704 | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=26061753  }} </ref><ref name="pmid30346624">{{cite journal| author=Diplas BH, Liu H, Yang R, Hansen LJ, Zachem AL, Zhao F et al.| title=Sensitive and rapid detection of TERT promoter and IDH mutations in diffuse gliomas. | journal=Neuro Oncol | year= 2019 | volume= 21 | issue= 4 | pages= 440-450 | pmid=30346624 | doi=10.1093/neuonc/noy167 | pmc=6422442 | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=30346624  }} </ref><ref name="pmid26617880">{{cite journal| author=Sun ZL, Chan AK, Chen LC, Tang C, Zhang ZY, Ding XJ et al.| title=TERT promoter mutated WHO grades II and III gliomas are located preferentially in the frontal lobe and avoid the midline. | journal=Int J Clin Exp Pathol | year= 2015 | volume= 8 | issue= 9 | pages= 11485-94 | pmid=26617880 | doi= | pmc=4637696 | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=26617880  }} </ref><ref name="pmid26957363">{{cite journal| author=Yang P, Cai J, Yan W, Zhang W, Wang Y, Chen B et al.| title=Classification based on mutations of TERT promoter and IDH characterizes subtypes in grade II/III gliomas. | journal=Neuro Oncol | year= 2016 | volume= 18 | issue= 8 | pages= 1099-108 | pmid=26957363 | doi=10.1093/neuonc/now021 | pmc=4933482 | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=26957363  }} </ref><ref name="pmid25314060">{{cite journal| author=Labussière M, Di Stefano AL, Gleize V, Boisselier B, Giry M, Mangesius S et al.| title=TERT promoter mutations in gliomas, genetic associations and clinico-pathological correlations. | journal=Br J Cancer | year= 2014 | volume= 111 | issue= 10 | pages= 2024-32 | pmid=25314060 | doi=10.1038/bjc.2014.538 | pmc=4229642 | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=25314060  }} </ref><ref name="pmid26608520">{{cite journal| author=Nencha U, Rahimian A, Giry M, Sechi A, Mokhtari K, Polivka M et al.| title=TERT promoter mutations and rs2853669 polymorphism: prognostic impact and interactions with common alterations in glioblastomas. | journal=J Neurooncol | year= 2016 | volume= 126 | issue= 3 | pages= 441-6 | pmid=26608520 | doi=10.1007/s11060-015-1999-3 | pmc= | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=26608520  }} </ref>
:*[[TERT]] [[promoter]]<ref name="pmid26061753">{{cite journal| author=Eckel-Passow JE, Lachance DH, Molinaro AM, Walsh KM, Decker PA, Sicotte H et al.| title=Glioma Groups Based on 1p/19q, IDH, and TERT Promoter Mutations in Tumors. | journal=N Engl J Med | year= 2015 | volume= 372 | issue= 26 | pages= 2499-508 | pmid=26061753 | doi=10.1056/NEJMoa1407279 | pmc=4489704 | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=26061753  }} </ref><ref name="pmid30346624">{{cite journal| author=Diplas BH, Liu H, Yang R, Hansen LJ, Zachem AL, Zhao F et al.| title=Sensitive and rapid detection of TERT promoter and IDH mutations in diffuse gliomas. | journal=Neuro Oncol | year= 2019 | volume= 21 | issue= 4 | pages= 440-450 | pmid=30346624 | doi=10.1093/neuonc/noy167 | pmc=6422442 | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=30346624  }} </ref><ref name="pmid26617880">{{cite journal| author=Sun ZL, Chan AK, Chen LC, Tang C, Zhang ZY, Ding XJ et al.| title=TERT promoter mutated WHO grades II and III gliomas are located preferentially in the frontal lobe and avoid the midline. | journal=Int J Clin Exp Pathol | year= 2015 | volume= 8 | issue= 9 | pages= 11485-94 | pmid=26617880 | doi= | pmc=4637696 | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=26617880  }} </ref><ref name="pmid26957363">{{cite journal| author=Yang P, Cai J, Yan W, Zhang W, Wang Y, Chen B et al.| title=Classification based on mutations of TERT promoter and IDH characterizes subtypes in grade II/III gliomas. | journal=Neuro Oncol | year= 2016 | volume= 18 | issue= 8 | pages= 1099-108 | pmid=26957363 | doi=10.1093/neuonc/now021 | pmc=4933482 | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=26957363  }} </ref><ref name="pmid25314060">{{cite journal| author=Labussière M, Di Stefano AL, Gleize V, Boisselier B, Giry M, Mangesius S et al.| title=TERT promoter mutations in gliomas, genetic associations and clinico-pathological correlations. | journal=Br J Cancer | year= 2014 | volume= 111 | issue= 10 | pages= 2024-32 | pmid=25314060 | doi=10.1038/bjc.2014.538 | pmc=4229642 | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=25314060  }} </ref><ref name="pmid26608520">{{cite journal| author=Nencha U, Rahimian A, Giry M, Sechi A, Mokhtari K, Polivka M et al.| title=TERT promoter mutations and rs2853669 polymorphism: prognostic impact and interactions with common alterations in glioblastomas. | journal=J Neurooncol | year= 2016 | volume= 126 | issue= 3 | pages= 441-6 | pmid=26608520 | doi=10.1007/s11060-015-1999-3 | pmc= | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=26608520  }} </ref>
:*[[H3F3A|H3]] K27M [[mutations]] in either ''[[H3F3A]]'' (one of two [[genes]] [[Encoding (memory)|encoding]] the [[histone]] H3.3 variant) or ''[[HIST1H3B]]/[[HIST1H3C|C]]'' ([[Encoding (memory)|encoding]] the [[histone]] H3.1 variant)<ref name="pmid22661320">{{cite journal| author=Khuong-Quang DA, Buczkowicz P, Rakopoulos P, Liu XY, Fontebasso AM, Bouffet E et al.| title=K27M mutation in histone H3.3 defines clinically and biologically distinct subgroups of pediatric diffuse intrinsic pontine gliomas. | journal=Acta Neuropathol | year= 2012 | volume= 124 | issue= 3 | pages= 439-47 | pmid=22661320 | doi=10.1007/s00401-012-0998-0 | pmc=3422615 | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=22661320  }} </ref><ref name="pmid30890717">{{cite journal| author=Harutyunyan AS, Krug B, Chen H, Papillon-Cavanagh S, Zeinieh M, De Jay N et al.| title=H3K27M induces defective chromatin spread of PRC2-mediated repressive H3K27me2/me3 and is essential for glioma tumorigenesis. | journal=Nat Commun | year= 2019 | volume= 10 | issue= 1 | pages= 1262 | pmid=30890717 | doi=10.1038/s41467-019-09140-x | pmc=6425035 | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=30890717  }} </ref><ref name="pmid22286216">{{cite journal| author=Wu G, Broniscer A, McEachron TA, Lu C, Paugh BS, Becksfort J et al.| title=Somatic histone H3 alterations in pediatric diffuse intrinsic pontine gliomas and non-brainstem glioblastomas. | journal=Nat Genet | year= 2012 | volume= 44 | issue= 3 | pages= 251-3 | pmid=22286216 | doi=10.1038/ng.1102 | pmc=3288377 | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=22286216  }} </ref><ref name="pmid26399631">{{cite journal| author=Castel D, Philippe C, Calmon R, Le Dret L, Truffaux N, Boddaert N et al.| title=Histone H3F3A and HIST1H3B K27M mutations define two subgroups of diffuse intrinsic pontine gliomas with different prognosis and phenotypes. | journal=Acta Neuropathol | year= 2015 | volume= 130 | issue= 6 | pages= 815-27 | pmid=26399631 | doi=10.1007/s00401-015-1478-0 | pmc=4654747 | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=26399631  }} </ref><ref name="pmid27038188">{{cite journal| author=Castel D, Grill J, Debily MA| title=Histone H3 genotyping refines clinico-radiological diagnostic and prognostic criteria in DIPG. | journal=Acta Neuropathol | year= 2016 | volume= 131 | issue= 5 | pages= 795-6 | pmid=27038188 | doi=10.1007/s00401-016-1568-7 | pmc=4835508 | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=27038188  }} </ref><ref name="pmid28522693">{{cite journal| author=Cordero FJ, Huang Z, Grenier C, He X, Hu G, McLendon RE et al.| title=Histone H3.3K27M Represses p16 to Accelerate Gliomagenesis in a Murine Model of DIPG. | journal=Mol Cancer Res | year= 2017 | volume= 15 | issue= 9 | pages= 1243-1254 | pmid=28522693 | doi=10.1158/1541-7786.MCR-16-0389 | pmc=5581686 | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=28522693  }} </ref>
:*[[H3F3A|H3]] K27M [[mutations]] in either ''[[H3F3A]]'' (one of two [[genes]] [[Encoding (memory)|encoding]] the [[histone]] H3.3 variant) or ''[[HIST1H3B]]/[[HIST1H3C|C]]'' ([[Encoding (memory)|encoding]] the [[histone]] H3.1 variant).<ref name="pmid22661320">{{cite journal| author=Khuong-Quang DA, Buczkowicz P, Rakopoulos P, Liu XY, Fontebasso AM, Bouffet E et al.| title=K27M mutation in histone H3.3 defines clinically and biologically distinct subgroups of pediatric diffuse intrinsic pontine gliomas. | journal=Acta Neuropathol | year= 2012 | volume= 124 | issue= 3 | pages= 439-47 | pmid=22661320 | doi=10.1007/s00401-012-0998-0 | pmc=3422615 | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=22661320  }} </ref><ref name="pmid30890717">{{cite journal| author=Harutyunyan AS, Krug B, Chen H, Papillon-Cavanagh S, Zeinieh M, De Jay N et al.| title=H3K27M induces defective chromatin spread of PRC2-mediated repressive H3K27me2/me3 and is essential for glioma tumorigenesis. | journal=Nat Commun | year= 2019 | volume= 10 | issue= 1 | pages= 1262 | pmid=30890717 | doi=10.1038/s41467-019-09140-x | pmc=6425035 | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=30890717  }} </ref><ref name="pmid22286216">{{cite journal| author=Wu G, Broniscer A, McEachron TA, Lu C, Paugh BS, Becksfort J et al.| title=Somatic histone H3 alterations in pediatric diffuse intrinsic pontine gliomas and non-brainstem glioblastomas. | journal=Nat Genet | year= 2012 | volume= 44 | issue= 3 | pages= 251-3 | pmid=22286216 | doi=10.1038/ng.1102 | pmc=3288377 | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=22286216  }} </ref><ref name="pmid26399631">{{cite journal| author=Castel D, Philippe C, Calmon R, Le Dret L, Truffaux N, Boddaert N et al.| title=Histone H3F3A and HIST1H3B K27M mutations define two subgroups of diffuse intrinsic pontine gliomas with different prognosis and phenotypes. | journal=Acta Neuropathol | year= 2015 | volume= 130 | issue= 6 | pages= 815-27 | pmid=26399631 | doi=10.1007/s00401-015-1478-0 | pmc=4654747 | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=26399631  }} </ref><ref name="pmid27038188">{{cite journal| author=Castel D, Grill J, Debily MA| title=Histone H3 genotyping refines clinico-radiological diagnostic and prognostic criteria in DIPG. | journal=Acta Neuropathol | year= 2016 | volume= 131 | issue= 5 | pages= 795-6 | pmid=27038188 | doi=10.1007/s00401-016-1568-7 | pmc=4835508 | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=27038188  }} </ref><ref name="pmid28522693">{{cite journal| author=Cordero FJ, Huang Z, Grenier C, He X, Hu G, McLendon RE et al.| title=Histone H3.3K27M Represses p16 to Accelerate Gliomagenesis in a Murine Model of DIPG. | journal=Mol Cancer Res | year= 2017 | volume= 15 | issue= 9 | pages= 1243-1254 | pmid=28522693 | doi=10.1158/1541-7786.MCR-16-0389 | pmc=5581686 | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=28522693  }} </ref>
:*''[[mutation|NJDS]]'' (A 2009 [[Oxford Forum|Oxford]] Neurosymposium [[Study design|study]] illustrated that there's a 69% [[correlation]] between NJDS [[gene mutation]] and [[tumor]] [[Initiation (chemistry)|initiation]])
:*''[[mutation|NJDS]]'' (A 2009 [[Oxford Forum|Oxford]] Neurosymposium [[Study design|study]] illustrated that there's a 69% [[correlation]] between NJDS [[gene mutation]] and [[tumor]] [[Initiation (chemistry)|initiation]]).
:*''[[CIC (gene)|CIC]]''<ref name="pmid24086756">{{cite journal| author=Eisenreich S, Abou-El-Ardat K, Szafranski K, Campos Valenzuela JA, Rump A, Nigro JM et al.| title=Novel CIC point mutations and an exon-spanning, homozygous deletion identified in oligodendroglial tumors by a comprehensive genomic approach including transcriptome sequencing. | journal=PLoS One | year= 2013 | volume= 8 | issue= 9 | pages= e76623 | pmid=24086756 | doi=10.1371/journal.pone.0076623 | pmc=3785522 | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=24086756  }} </ref><ref name="pmid22072542">{{cite journal| author=Yip S, Butterfield YS, Morozova O, Chittaranjan S, Blough MD, An J et al.| title=Concurrent CIC mutations, IDH mutations, and 1p/19q loss distinguish oligodendrogliomas from other cancers. | journal=J Pathol | year= 2012 | volume= 226 | issue= 1 | pages= 7-16 | pmid=22072542 | doi=10.1002/path.2995 | pmc=3246739 | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=22072542  }} </ref>
:*''[[CIC (gene)|CIC]]''<ref name="pmid24086756">{{cite journal| author=Eisenreich S, Abou-El-Ardat K, Szafranski K, Campos Valenzuela JA, Rump A, Nigro JM et al.| title=Novel CIC point mutations and an exon-spanning, homozygous deletion identified in oligodendroglial tumors by a comprehensive genomic approach including transcriptome sequencing. | journal=PLoS One | year= 2013 | volume= 8 | issue= 9 | pages= e76623 | pmid=24086756 | doi=10.1371/journal.pone.0076623 | pmc=3785522 | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=24086756  }} </ref><ref name="pmid22072542">{{cite journal| author=Yip S, Butterfield YS, Morozova O, Chittaranjan S, Blough MD, An J et al.| title=Concurrent CIC mutations, IDH mutations, and 1p/19q loss distinguish oligodendrogliomas from other cancers. | journal=J Pathol | year= 2012 | volume= 226 | issue= 1 | pages= 7-16 | pmid=22072542 | doi=10.1002/path.2995 | pmc=3246739 | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=22072542  }} </ref>
:*''[[Far upstream element-binding protein 1|FUBP1]]''
:*''[[Far upstream element-binding protein 1|FUBP1]]''
Line 34: Line 34:
:*''[[EGFR]]''
:*''[[EGFR]]''
:*''[[PTEN]]''
:*''[[PTEN]]''
*There is a [[strong]] [[Association (statistics)|association]] of [[oligodendroglioma]] with [[expression]] of [[receptor tyrosine kinases]] that activate [[Phosphoinositide 3-kinase|PI3K]]/[[AKT]], [[RAS]]/[[MAP]], and [[PLC]]/[[PKC alpha|PKC]] pathways<ref name="von DeimlingHartmann2005">{{cite journal|last1=von Deimling|first1=A|last2=Hartmann|first2=C|title=Oligodendrogliomas: Impact of molecular genetics on treatment|journal=Neurology India|volume=53|issue=2|year=2005|pages=140|issn=0028-3886|doi=10.4103/0028-3886.16394}}</ref>
*There is a [[strong]] [[Association (statistics)|association]] of [[oligodendroglioma]] with [[expression]] of [[receptor tyrosine kinases]] that activate [[Phosphoinositide 3-kinase|PI3K]]/[[AKT]], [[RAS]]/[[MAP]], and [[PLC]]/[[PKC alpha|PKC]] pathways.<ref name="von DeimlingHartmann2005">{{cite journal|last1=von Deimling|first1=A|last2=Hartmann|first2=C|title=Oligodendrogliomas: Impact of molecular genetics on treatment|journal=Neurology India|volume=53|issue=2|year=2005|pages=140|issn=0028-3886|doi=10.4103/0028-3886.16394}}</ref>


===Gross Pathology===
===Gross Pathology===
*On [[gross pathology]], [[oligodendroglioma]] is characterized by a well-circumscribed, [[Gelatinase|gelatinous]], [[gray]] [[mass]] which may [[Expanded access|expand]] a [[gyrus]] and remodel the [[skull]]<ref name="grosspa">Gross appearance of oligodendroglioma. Dr Henry Knipe and Dr Frank Gaillard et al. http://radiopaedia.org/articles/oligodendroglioma</ref>
*On [[gross pathology]], [[oligodendroglioma]] is characterized by a well-circumscribed, [[Gelatinase|gelatinous]], [[gray]] [[mass]] which may [[Expanded access|expand]] a [[gyrus]] and remodel the [[skull|skul.l]]<ref name="grosspa">Gross appearance of oligodendroglioma. Dr Henry Knipe and Dr Frank Gaillard et al. http://radiopaedia.org/articles/oligodendroglioma</ref>
*Other [[Characteristic function (probability theory)|characteristic]] [[Gross pathology|gross pathological]] [[Features (pattern recognition)|features]] [[Association (statistics)|associated]] with [[oligodendroglioma]] include:<ref name="grosspa">Gross appearance of oligodendroglioma. Dr Henry Knipe and Dr Frank Gaillard et al. http://radiopaedia.org/articles/oligodendroglioma</ref><ref name="von DeimlingHartmann2005">{{cite journal|last1=von Deimling|first1=A|last2=Hartmann|first2=C|title=Oligodendrogliomas: Impact of molecular genetics on treatment|journal=Neurology India|volume=53|issue=2|year=2005|pages=140|issn=0028-3886|doi=10.4103/0028-3886.16394}}</ref>
*Other [[Characteristic function (probability theory)|characteristic]] [[Gross pathology|gross pathological]] [[Features (pattern recognition)|features]] [[Association (statistics)|associated]] with [[oligodendroglioma]] include:<ref name="grosspa">Gross appearance of oligodendroglioma. Dr Henry Knipe and Dr Frank Gaillard et al. http://radiopaedia.org/articles/oligodendroglioma</ref><ref name="von DeimlingHartmann2005">{{cite journal|last1=von Deimling|first1=A|last2=Hartmann|first2=C|title=Oligodendrogliomas: Impact of molecular genetics on treatment|journal=Neurology India|volume=53|issue=2|year=2005|pages=140|issn=0028-3886|doi=10.4103/0028-3886.16394}}</ref>
 
**[[Calcification]] (70-90%; one of the most [[Frequentism|frequently]] [[Calcification|calcifying]] [[tumors]])
:*[[Calcification]] (70-90%; one of the most [[Frequentism|frequently]] [[Calcification|calcifying]] [[tumors]])
**[[Hemorrhage|Focal hemorrhage]]
:*[[Hemorrhage|Focal hemorrhage]]
**[[cyst|Cystic]] (20%)
:*[[cyst|Cystic]] (20%)
*Common intracranial sites [[Association (statistics)|associated]] with [[oligodendroglioma]] include:<ref name="gross">Gross/radiologic findings of oligodendroglioma. Libre Pathology. http://librepathology.org/wiki/index.php/Oligodendroglioma</ref>
*Common intracranial sites [[Association (statistics)|associated]] with [[oligodendroglioma]] include:<ref name="gross">Gross/radiologic findings of oligodendroglioma. Libre Pathology. http://librepathology.org/wiki/index.php/Oligodendroglioma</ref>
:*[[Cerebral hemisphere]]s ([[cortex]] and [[white matter]]) - [[Distribution (pharmacology)|distribution]] between [[frontal lobe|frontal]] (most common, > 50% of cases), [[parietal lobe|parietal]], [[temporal lobe|temporal]], and [[occipital lobe]] approximates 3:2:2:1
**[[Cerebral hemisphere]]s ([[cortex]] and [[white matter]]) - [[Distribution (pharmacology)|distribution]] between [[frontal lobe|frontal]] (most common, > 50% of cases), [[parietal lobe|parietal]], [[temporal lobe|temporal]], and [[occipital lobe]] approximates 3:2:2:1.
:*[[Posterior fossa]] ([[rare]])
**[[Posterior fossa]] ([[rare]])
:*[[spinal cord|Intramedullary spinal cord]] (very [[rare]], only 1.5% of [[oligodendrogliomas]])
**[[spinal cord|Intramedullary spinal cord]] (very [[rare]], only 1.5% of [[oligodendrogliomas]]).
{|
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[[File:Oligogross.jpg|thumb|250px|none| Oligodendroglioma involving frontal lobe [http://peir.path.uab.edu/library/picture.php?/18102]]]
|
[[File:Mixedoligo.jpg|thumb|250px|none| Mixed astrocytoma and oligodendroglioma [http://peir.path.uab.edu/library/picture.php?/18103/categories]]]
|
[[File:Oliggross.jpg|thumb|250px|none| Oligodendroglioma gross appearance [http://peir.path.uab.edu/library/picture.php?/18104/categories]]]
|}


===Microscopic Pathology===
===Microscopic Pathology===
On microscopic histopathological analysis, oligodendroglioma is characterized by:<ref name="von DeimlingHartmann2005">{{cite journal|last1=von Deimling|first1=A|last2=Hartmann|first2=C|title=Oligodendrogliomas: Impact of molecular genetics on treatment|journal=Neurology India|volume=53|issue=2|year=2005|pages=140|issn=0028-3886|doi=10.4103/0028-3886.16394}}</ref><ref name="micro">Microscopic features of oligodendroglioma. Libre Pathology. http://librepathology.org/wiki/index.php/Oligodendroglioma</ref><ref name="turk">{{Citation |last=Ersen |first=Ayca|year=2008 |title=Pathology of malignant gliomas: Challenges of everyday practice and the WHO 2007 |publisher=Turkish Journal of Pathology |publication-place= |page= |url=http://www.turkjpath.org/text.php3?id=645 |accessdate=9 October, 2015 }}</ref><ref name="pmid15509821">{{cite journal| author=Eskandar EN, Loeffler JS, O'Neill AM, Hunter GJ, Louis DN| title=Case records of the Massachusetts General Hospital. Weekly clinicopathological exercises. Case 33-2004. A 34-year-old man with a seizure and a frontal-lobe brain lesion. | journal=N Engl J Med | year= 2004 | volume= 351 | issue= 18 | pages= 1875-82 | pmid=15509821 | doi=10.1056/NEJMcpc049025 | pmc= | url=http://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=15509821  }} </ref><ref name="pmid22941225">{{cite journal| author=Rodriguez FJ, Perry A, Rosenblum MK, Krawitz S, Cohen KJ, Lin D et al.| title=Disseminated oligodendroglial-like leptomeningeal tumor of childhood: a distinctive clinicopathologic entity. | journal=Acta Neuropathol | year= 2012 | volume= 124 | issue= 5 | pages= 627-41 | pmid=22941225 | doi=10.1007/s00401-012-1037-x | pmc= | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=22941225  }} </ref>
On [[microscopic]] [[histopathological]] [[analysis]], [[oligodendroglioma]] is characterized by:<ref name="von DeimlingHartmann2005">{{cite journal|last1=von Deimling|first1=A|last2=Hartmann|first2=C|title=Oligodendrogliomas: Impact of molecular genetics on treatment|journal=Neurology India|volume=53|issue=2|year=2005|pages=140|issn=0028-3886|doi=10.4103/0028-3886.16394}}</ref><ref name="micro">Microscopic features of oligodendroglioma. Libre Pathology. http://librepathology.org/wiki/index.php/Oligodendroglioma</ref><ref name="turk">{{Citation |last=Ersen |first=Ayca|year=2008 |title=Pathology of malignant gliomas: Challenges of everyday practice and the WHO 2007 |publisher=Turkish Journal of Pathology |publication-place= |page= |url=http://www.turkjpath.org/text.php3?id=645 |accessdate=9 October, 2015 }}</ref><ref name="pmid15509821">{{cite journal| author=Eskandar EN, Loeffler JS, O'Neill AM, Hunter GJ, Louis DN| title=Case records of the Massachusetts General Hospital. Weekly clinicopathological exercises. Case 33-2004. A 34-year-old man with a seizure and a frontal-lobe brain lesion. | journal=N Engl J Med | year= 2004 | volume= 351 | issue= 18 | pages= 1875-82 | pmid=15509821 | doi=10.1056/NEJMcpc049025 | pmc= | url=http://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=15509821  }} </ref><ref name="pmid22941225">{{cite journal| author=Rodriguez FJ, Perry A, Rosenblum MK, Krawitz S, Cohen KJ, Lin D et al.| title=Disseminated oligodendroglial-like leptomeningeal tumor of childhood: a distinctive clinicopathologic entity. | journal=Acta Neuropathol | year= 2012 | volume= 124 | issue= 5 | pages= 627-41 | pmid=22941225 | doi=10.1007/s00401-012-1037-x | pmc= | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=22941225  }} </ref>
*Diffusely growing, infiltrative tumor
*[[Diffuse|Diffusely]] [[Growth|growing]], [[Infiltration (medical)|infiltrative]] [[tumor]]
*Moderate cellularity
*Moderate [[Cellular|cellularity]]
*Highly cellular lesion composed of typically monomorphic cells resembling ''fried eggs'' with:
*Highly [[cellular]] [[lesion]] composed of [[Typical set|typically]] monomorphic [[Cells (biology)|cells]] resembling ''fried [[Egg (biology)|eggs]]'' with:
**[[nucleus|Round nucleus]] - key feature
**[[nucleus|Round nucleus]] - key [[Features (pattern recognition)|feature]]
**Distinct cell borders
**[[Distinctive feature|Distinct]] [[Cell (biology)|cell]] borders
**Moderate-to-marked [[atypia|nuclear atypia]] with speckled "''salt-and-pepper''" chromatin pattern
**Moderate-to-marked [[atypia|nuclear atypia]] with [[Speckle pattern|speckled]] "''[[salt]]-and-[[Pepper spray|pepper]]''" [[chromatin]] [[pattern]]
**Inconspicuous nucleoli
**Inconspicuous [[nucleoli]]
**[[cytoplasm|Clear cytoplasm]]  (artifactual retraction of the cytoplasm on routinely processed formalin fixed, paraffin embedded material, leading to the characteristic "fried egg" appearance)
**[[cytoplasm|Clear cytoplasm]]  (artifactual [[retraction]] of the [[cytoplasm]] on routinely [[Process (anatomy)|processed]] [[formalin]] [[Fixed effects|fixed]], [[paraffin]] [[Embedded value|embedded]] [[Materials science|material]], [[Leading strand|leading]] to the [[Characteristic function (probability theory)|characteristic]] "fried [[Egg (biology)|egg]]" [[appearance]]).
***Some oligodendrogliomas have [[eosinophilic]] cytoplasm with focal perinuclear clearing
***Some [[oligodendrogliomas]] have [[eosinophilic]] [[cytoplasm]] with focal [[Perinuclear space|perinuclear]] clearing.
**Dense network of acutely fine branched capillary sized vessels -classically referred to as a "''chicken-wire''" like appearance/pattern<ref name="microscope">Images of microscopic appearance of oligodendroglioma. Wikipedia 2015. https://en.wikipedia.org/wiki/Oligodendroglioma</ref>
**[[Dense]] [[Network motif|network]] of [[Acute|acutely]] fine branched [[capillary]] [[Size consistency|sized]] [[vessels]] -classically [[Reference|referred]] to as a "''chicken-wire''" like [[appearance]]/[[pattern|pattern.]]<ref name="microscope">Images of microscopic appearance of oligodendroglioma. Wikipedia 2015. https://en.wikipedia.org/wiki/Oligodendroglioma</ref>
***Abundant and delicate appearing; may vaguely resemble a [[paraganglioma]] at low power
***Abundant and delicate [[Appearance|appearing]]; may [[Vagueness|vaguely]] resemble a [[paraganglioma]] at low [[Power nap|power]].
*Small punctate [[calcification]]s, particularly along the blood vessels is a striking feature (but not a specific finding)
*Small punctate [[calcification]]s, particularly along the [[blood vessels]] is a striking [[Features (pattern recognition)|feature]] (but not a [[Specific activity|specific]] finding).
*Perifocal [[edema]] - rare
*Perifocal [[edema]] - [[rare]]
*Few tumors may exhibit [[eosinophilic]] granular bodies
*[[Fewmets|Few]] [[tumors]] may [[Exhibitionism|exhibit]] [[eosinophilic]] [[Granular cell|granular]] [[Body|bodies]]
*Some tumors may show a spongioblastoma-like growth pattern
*Some [[tumors]] may show a [[spongioblastoma]]-like [[growth]] [[pattern]]
*Tumor cells may form following secondary structures in the surrounding infiltrated brain parenchyma:
*[[Tumor cell|Tumor cells]] may form following [[Secondary structure|secondary structures]] in the surrounding [[Infiltration (medical)|infiltrated]] [[brain]] [[parenchyma]]:
**Perineuronal satellitosis
**Perineuronal satellitosis
**Subpial accumulation
**[[Subpial space|Subpial]] accumulation
**Perivascular distribution (less common)
**[[Perivascular cell|Perivascular]] [[Distribution (pharmacology)|distribution]] (less common)
*Microgemistocytic appearance of tumor cells with a rounded belly of eccentric GFAP+ eosinophilic cytoplasm (maybe present)<ref name="pmid2205356">{{cite journal| author=Kros JM, Van Eden CG, Stefanko SZ, Waayer-Van Batenburg M, van der Kwast TH| title=Prognostic implications of glial fibrillary acidic protein containing cell types in oligodendrogliomas. | journal=Cancer | year= 1990 | volume= 66 | issue= 6 | pages= 1204-12 | pmid=2205356 | doi= | pmc= | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=2205356  }} </ref>
*Microgemistocytic [[appearance]] of [[Tumor cell|tumor cells]] with a rounded [[belly]] of [[Eccentricity (mathematics)|eccentric]] [[Glial fibrillary acidic protein|GFAP]]+ [[eosinophilic]] [[cytoplasm]] (maybe present).<ref name="pmid2205356">{{cite journal| author=Kros JM, Van Eden CG, Stefanko SZ, Waayer-Van Batenburg M, van der Kwast TH| title=Prognostic implications of glial fibrillary acidic protein containing cell types in oligodendrogliomas. | journal=Cancer | year= 1990 | volume= 66 | issue= 6 | pages= 1204-12 | pmid=2205356 | doi= | pmc= | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=2205356  }} </ref>
*A predominant fibrillar astrocytic phenotype is compatible with the diagnosis when following appropriate molecular findings are present:<ref name="pmid26061751">{{cite journal| author=Cancer Genome Atlas Research Network. Brat DJ, Verhaak RG, Aldape KD, Yung WK, Salama SR et al.| title=Comprehensive, Integrative Genomic Analysis of Diffuse Lower-Grade Gliomas. | journal=N Engl J Med | year= 2015 | volume= 372 | issue= 26 | pages= 2481-98 | pmid=26061751 | doi=10.1056/NEJMoa1402121 | pmc=4530011 | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=26061751  }} </ref>
*A predominant [[Fibrillarin|fibrillar]] [[astrocytic]] [[phenotype]] is compatible with the [[diagnosis]] when following [[Appropriate Use Criteria|appropriate]] [[molecular]] findings are present:<ref name="pmid26061751">{{cite journal| author=Cancer Genome Atlas Research Network. Brat DJ, Verhaak RG, Aldape KD, Yung WK, Salama SR et al.| title=Comprehensive, Integrative Genomic Analysis of Diffuse Lower-Grade Gliomas. | journal=N Engl J Med | year= 2015 | volume= 372 | issue= 26 | pages= 2481-98 | pmid=26061751 | doi=10.1056/NEJMoa1402121 | pmc=4530011 | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=26061751  }} </ref>
**''IDH'' mutation
**''[[IDH1|IDH]]'' [[mutation]]
**1p/19q codeletion
**[[1p36 deletion syndrome|1p]]/19q codeletion
{|
|
[[File:Olighe.jpg|thumb|250px|none| Oligodendroglioma HE stain [https://commons.wikimedia.org/wiki/Category:Histopathology_of_oligodendroglioma#/media/File:Image_NP_T4a1_0004.JPG]]]
|
[[File:1200px-Oligodendroglioma discrete invasion HE.jpg|thumb|250px|none|Low power magnification of a Oligodendroglioma biopsy specimen showing discrete infiltration of the surrounding brain [https://librepathology.org/wiki/File:Oligodendroglioma_discrete_invasion_HE.jpg]]]
|
[[File:Oligo hee.jpg|thumb|250px|none| Oligodendroglioma HE stain [https://commons.wikimedia.org/wiki/Category:Histopathology_of_oligodendroglioma#/media/File:Image_NP_T4a1_0002.JPG]]]
|
[[File:Oligo hne.jpg|thumb|250px|none| Oligodendroglioma HE stain [https://commons.wikimedia.org/wiki/Category:Histopathology_of_oligodendroglioma#/media/File:Image_NP_T4a1_0001.JPG]]]
|
|}
{|
|
[[File:Oligohe.jpg|thumb|250px|none| Oligodendroglioma HE stain [https://commons.wikimedia.org/wiki/Category:Histopathology_of_oligodendroglioma#/media/File:Image_NP_T4a1_0003.JPG]]]
|
[[File:Oligodendorglioma GFAP.jpg|thumb|250px|none| GFAP immunohistochemistry in a histopathology specimen of oligodendroglioma grade II WHO [https://commons.wikimedia.org/wiki/Category:Histopathology_of_oligodendroglioma#/media/File:Oligodendorglioma_GFAP.jpg]]]
|
[[File:Oligodendroglioma histo.jpg|thumb|250px|none| High magnification micrograph of an oligodendroglioma showing the characteristic branching, small, chicken wire-like blood vessels and fried egg-like cells, with clear cytoplasm and well-defined cell borders. H&E stain. [https://commons.wikimedia.org/wiki/File:Oligodendroglioma1_high_mag.jpg]]]
|
[[File:Oligo low mag.jpg|thumb|250px|none|Low magnification micrograph of an oligodendroglioma showing the characteristic, small, branching, chicken wire-like blood vessels. H&E stain. [https://commons.wikimedia.org/wiki/File:Oligodendroglioma1_low_mag.jpg]]]
|
|}
====Microscopic histopathological findings in anaplastic oligodendroglioma====
====Microscopic histopathological findings in anaplastic oligodendroglioma====
On [[microscopic]] [[histopathological]] [[analysis]], [[anaplastic|anaplastic oligodendroglioma]], ''[[IDH1|IDH]]'' [[mutant]] and [[1p36 deletion syndrome|1p]]/19q codeleted, is characterized by:<ref name="micro">Microscopic features of oligodendroglioma. Libre Pathology. http://librepathology.org/wiki/index.php/Oligodendroglioma</ref>
On [[microscopic]] [[histopathological]] [[analysis]], [[anaplastic|anaplastic oligodendroglioma]], ''[[IDH1|IDH]]'' [[mutant]] and [[1p36 deletion syndrome|1p]]/19q codeleted, is characterized by:<ref name="micro">Microscopic features of oligodendroglioma. Libre Pathology. http://librepathology.org/wiki/index.php/Oligodendroglioma</ref>
Line 86: Line 115:
***[[Glomerular|Glomeruloid]]' [[vessels]] or
***[[Glomerular|Glomeruloid]]' [[vessels]] or
***[[Endothelial]] [[hyperplasia]]
***[[Endothelial]] [[hyperplasia]]
{|
|
[[File:Brisk mitotic rate.jpg|thumb|250px|none|Brisk mitotic rate in anaplastic oligodendroglioma [http://www.pathologyoutlines.com/topic/cnstumoranaplasticoligodendroglioma.html]]]
[[File:Brisk mitotic rate.jpg|thumb|250px|none|Brisk mitotic rate in anaplastic oligodendroglioma [http://www.pathologyoutlines.com/topic/cnstumoranaplasticoligodendroglioma.html]]]
{|
|
|
[[File:Oligodendroglioma histo.jpg|thumb|250px|none| High magnification micrograph of an oligodendroglioma showing the characteristic branching, small, chicken wire-like blood vessels and fried egg-like cells, with clear cytoplasm and well-defined cell borders. H&E stain. [https://commons.wikimedia.org/wiki/File:Oligodendroglioma1_high_mag.jpg]]]
[[File:Vascularproliferationoligo.jpg|thumb|250px|none| Vascularproliferation [https://emedicine.medscape.com/article/1743896-overview Source: Roger E McLendon, MD et al.]]]
|
|
[[File:Oligo low mag.jpg|thumb|250px|none|Low magnification micrograph of an oligodendroglioma showing the characteristic, small, branching, chicken wire-like blood vessels. H&E stain. [https://commons.wikimedia.org/wiki/File:Oligodendroglioma1_low_mag.jpg]]]
[[File:1200px-MAP2 anaplastic oligodendroglioma.jpg|thumb|250px|none|Histopathology of anaplastic oligodendroglioma (MAP2 staining) showing perinuclear immunoreactivity of tumor cells[https://librepathology.org/wiki/File:MAP2_anaplastic_oligodendroglioma.jpg]]]
|
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[[File:Fried egg app.jpg|thumb|250px|none| "Fried egg" appearance [http://www.pathologyoutlines.com/topic/cnstumoroligodendrogliomaidhmutant.html Source: John DeWitt, M.D., Ph.D.]]]
[[File:Fried egg app.jpg|thumb|250px|none| "Fried egg" appearance [http://www.pathologyoutlines.com/topic/cnstumoroligodendrogliomaidhmutant.html Source: John DeWitt, M.D., Ph.D.]]]
|
|}
{|
|
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[[File:Chickenwire vessels.jpg|thumb|250px|none| Chicken wire vessels [http://www.pathologyoutlines.com/topic/cnstumoroligodendrogliomaidhmutant.html Source: John DeWitt, M.D., Ph.D.]]]
[[File:Chickenwire vessels.jpg|thumb|250px|none| Chicken wire vessels [http://www.pathologyoutlines.com/topic/cnstumoroligodendrogliomaidhmutant.html Source: John DeWitt, M.D., Ph.D.]]]
|-
|
|
[[File:Friedeggoligo.jpg|thumb|250px|none| "Fried egg" appearance [http://www.pathologyoutlines.com/topic/cnstumoroligodendrogliomaidhmutant.html Source: John DeWitt, M.D., Ph.D.]]]
[[File:Friedeggoligo.jpg|thumb|250px|none| "Fried egg" appearance [http://www.pathologyoutlines.com/topic/cnstumoroligodendrogliomaidhmutant.html Source: John DeWitt, M.D., Ph.D.]]]
|
|
[[File:Vascularproliferationoligo.jpg|thumb|250px|none| Vascularproliferation [https://emedicine.medscape.com/article/1743896-overview Source: Roger E McLendon, MD et al.]]]
[[File:Infilcortex.jpg|thumb|250px|none| Infiltrating cortex [http://www.pathologyoutlines.com/topic/cnstumoroligodendrogliomaidhmutant.html Source: John DeWitt, M.D., Ph.D.]]]
|
[[File:1200px-Anaplastic oligodendroglioma minigemistocytes.jpg|thumb|250px|none|Histopathology of anaplastic oligodendroglioma (HE stain) showing minigemistocytes and mitoses among tumor cells with perinuclear halo.[https://librepathology.org/wiki/File:Anaplastic_oligodendroglioma_minigemistocytes.jpg]]]
|
[[File:1200px-IDH1 R132H in anaplastic ologodendroglioma.jpg|thumb|250px|none| Histopathology of anaplastic oligodendroglioma (IDH1 R132H staining) showing immunoreactivity of tumor cells idicating presence of the isocitrate dehydrogenase 1 R132H mutation [https://librepathology.org/wiki/File:IDH1_R132H_in_anaplastic_ologodendroglioma.jpg]]]
|
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[[File:Infilcortex.jpg|thumb|250px|none| Infiltrating cortex [http://www.pathologyoutlines.com/topic/cnstumoroligodendrogliomaidhmutant.html Source: John DeWitt, M.D., Ph.D.]]]
|}
|}


Latest revision as of 13:31, 13 August 2019

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Editor-In-Chief: C. Michael Gibson, M.S., M.D. [16]Associate Editor(s)-in-Chief: Sara Mohsin, M.D.[17]Sujit Routray, M.D. [18]

Overview

Oligodendroglioma arises from the tripotential glial precursor cells and not from the bipotential oligodendrocytes. Genes associated with the pathogenesis of oligodendroglioma include t[1;19][q10;p10], ATRX, NJDS, IDH1, IDH2, TERT promoter, H3 K27M (H3F3A, HIST1H3B/C), CIC, FUBP1, p53, Leu-7, TCF-12, TP53,MGMT, TP73, BRAF, EGFR, and PTEN. Common intracranial sites involved by oligodendroglioma include cerebral hemispheres, posterior fossa, and intramedullary spinal cord. On gross pathology, oligodendroglioma is characterized by a well-circumscribed, gelatinous, calcified, cystic, gray mass with focal hemorrhage which may expand a gyrus and remodel the skull. On microscopic histopathological analysis, oligodendroglioma is characterized by diffuse growthpattern of highly cellular lesion of monomorphic cells having rounded nucleus with atypia, speckled "salt-and-pepper" chromatin pattern and perinuclear haloresembling fried eggs, distinct cell borders, clear cytoplasm, abundant calcification and "chicken-wire" like vascularity pattern. Oligodendroglioma is demonstrated by positivity to tumor markers such as IDH1-R132H, MAP2, GFAP, S-100, SOX10, EMA, ATRX, Ki-67, NSE, synaptophysin, OLIG1, and OLIG2.

Pathophysiology

Pathogenesis

Genetics

Gross Pathology

Oligodendroglioma involving frontal lobe [1]
Mixed astrocytoma and oligodendroglioma [2]
Oligodendroglioma gross appearance [3]

Microscopic Pathology

On microscopic histopathological analysis, oligodendroglioma is characterized by:[20][60][61][62][63]

Oligodendroglioma HE stain [4]
Low power magnification of a Oligodendroglioma biopsy specimen showing discrete infiltration of the surrounding brain [5]
Oligodendroglioma HE stain [6]
Oligodendroglioma HE stain [7]
Oligodendroglioma HE stain [8]
GFAP immunohistochemistry in a histopathology specimen of oligodendroglioma grade II WHO [9]
High magnification micrograph of an oligodendroglioma showing the characteristic branching, small, chicken wire-like blood vessels and fried egg-like cells, with clear cytoplasm and well-defined cell borders. H&E stain. [10]
Low magnification micrograph of an oligodendroglioma showing the characteristic, small, branching, chicken wire-like blood vessels. H&E stain. [11]

Microscopic histopathological findings in anaplastic oligodendroglioma

On microscopic histopathological analysis, anaplastic oligodendroglioma, IDH mutant and 1p/19q codeleted, is characterized by:[60]

Brisk mitotic rate in anaplastic oligodendroglioma [12]
Vascularproliferation Source: Roger E McLendon, MD et al.
Histopathology of anaplastic oligodendroglioma (MAP2 staining) showing perinuclear immunoreactivity of tumor cells[13]
"Fried egg" appearance Source: John DeWitt, M.D., Ph.D.
Chicken wire vessels Source: John DeWitt, M.D., Ph.D.
"Fried egg" appearance Source: John DeWitt, M.D., Ph.D.
Infiltrating cortex Source: John DeWitt, M.D., Ph.D.
Histopathology of anaplastic oligodendroglioma (HE stain) showing minigemistocytes and mitoses among tumor cells with perinuclear halo.[14]
Histopathology of anaplastic oligodendroglioma (IDH1 R132H staining) showing immunoreactivity of tumor cells idicating presence of the isocitrate dehydrogenase 1 R132H mutation [15]

Immunohistochemistry

Oligodendroglioma is demonstrated by positivity to tumor markers such as:[68][69][20][7]

Oligodendroglioma stains negative for:

References

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  2. ↑ Suzuki H, Aoki K, Chiba K, Sato Y, Shiozawa Y, Shiraishi Y; et al. (2015). "Mutational landscape and clonal architecture in grade II and III gliomas". Nat Genet. 47 (5): 458–68. doi:10.1038/ng.3273. PMID 25848751.
  3. ↑ Leeper HE, Caron AA, Decker PA, Jenkins RB, Lachance DH, Giannini C (2015). "IDH mutation, 1p19q codeletion and ATRX loss in WHO grade II gliomas". Oncotarget. 6 (30): 30295–305. doi:10.18632/oncotarget.4497. PMC 4745799. PMID 26210286.
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  17. ↑ Labreche K, Simeonova I, Kamoun A, Gleize V, Chubb D, Letouzé E; et al. (2015). "TCF12 is mutated in anaplastic oligodendroglioma". Nat Commun. 6: 7207. doi:10.1038/ncomms8207. PMC 4490400. PMID 26068201.
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  70. ↑ Kato Y (2015). "Specific monoclonal antibodies against IDH1/2 mutations as diagnostic tools for gliomas". Brain Tumor Pathol. 32 (1): 3–11. doi:10.1007/s10014-014-0202-4. PMID 25324168.


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