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==Overview==
==Overview==
When evaluating a patient for oligodendroglioma, you should take a detailed history of the presenting symptom (onset, duration, and progression), other associated symptoms, and a thorough past medical history review. Other specific areas of focus when obtaining the history include review of common risk factors such as [[family history]] of [[brain tumors]].<ref name="pmid21149253">{{cite journal| author=McCarthy BJ, Rankin KM, Aldape K, Bondy ML, Brännström T, Broholm H et al.| title=Risk factors for oligodendroglial tumors: a pooled international study. | journal=Neuro Oncol | year= 2011 | volume= 13 | issue= 2 | pages= 242-50 | pmid=21149253 | doi=10.1093/neuonc/noq173 | pmc=PMC3064625 | url=http://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=21149253  }} </ref> Common symptoms associated with oligodendroglioma include [[seizure]], [[headache]], [[nausea]], [[vomiting]], [[vertigo]], changes in speech, mood, and personality, [[visual loss]], [[diplopia]], [[strabismus]], [[hemiparesis|muscle weakness]], and [[numbness]].<ref name="pmid9684012">{{cite journal| author=Douay X, Daems-Monpeurt C, Labalette P, Blond S, Petit H| title=[Bilateral 3rd cranial nerve palsy disclosing oligodendroglioma]. | journal=Rev Neurol (Paris) | year= 1997 | volume= 153 | issue= 6-7 | pages= 430-2 | pmid=9684012 | doi= | pmc= | url=http://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=9684012  }} </ref><ref name="pmid17553214">{{cite journal| author=Hata N, Shono T, Mizoguchi M, Matsumoto K, Guan Y, Nagata S et al.| title=Loss of heterozygosity analysis in an anaplastic oligodendroglioma arising after radiation therapy. | journal=Neurol Res | year= 2007 | volume= 29 | issue= 7 | pages= 723-6 | pmid=17553214 | doi=10.1179/016164107X208068 | pmc= | url=http://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=17553214  }} </ref><ref name="pmid1695334">{{cite journal| author=Ogasawara H, Kiya K, Uozumi T, Sugiyama K, Kawamoto K, Ohta M| title=Multiple oligodendroglioma--case report. | journal=Neurol Med Chir (Tokyo) | year= 1990 | volume= 30 | issue= 2 | pages= 127-31 | pmid=1695334 | doi= | pmc= | url=http://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=1695334  }} </ref><ref name="pmid2308753">{{cite journal| author=Raciti-Daurio C, Caruso J| title=Oligodendroglioma--a case presentation. | journal=Optom Vis Sci | year= 1990 | volume= 67 | issue= 1 | pages= 56-8 | pmid=2308753 | doi= | pmc= | url=http://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=2308753  }} </ref>
When evaluating a patient for oligodendroglioma, you should take a detailed history of the presenting symptom (onset, duration, and progression), other associated symptoms, and a thorough past medical history review. Other specific areas of focus when obtaining the history include review of common risk factors such as [[family history]] of [[brain tumors]].<ref name="pmid21149253">{{cite journal| author=McCarthy BJ, Rankin KM, Aldape K, Bondy ML, Brännström T, Broholm H et al.| title=Risk factors for oligodendroglial tumors: a pooled international study. | journal=Neuro Oncol | year= 2011 | volume= 13 | issue= 2 | pages= 242-50 | pmid=21149253 | doi=10.1093/neuonc/noq173 | pmc=PMC3064625 | url=http://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=21149253  }} </ref> Symptoms associated with oligodendroglioma include [[seizure]], [[headache]], [[nausea]], [[vomiting]], [[vertigo]], changes in speech, mood, and personality, [[visual loss]], [[diplopia]], [[strabismus]], [[hemiparesis|muscle weakness]], and [[numbness]].<ref name="pmid9684012">{{cite journal| author=Douay X, Daems-Monpeurt C, Labalette P, Blond S, Petit H| title=[Bilateral 3rd cranial nerve palsy disclosing oligodendroglioma]. | journal=Rev Neurol (Paris) | year= 1997 | volume= 153 | issue= 6-7 | pages= 430-2 | pmid=9684012 | doi= | pmc= | url=http://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=9684012  }} </ref><ref name="pmid17553214">{{cite journal| author=Hata N, Shono T, Mizoguchi M, Matsumoto K, Guan Y, Nagata S et al.| title=Loss of heterozygosity analysis in an anaplastic oligodendroglioma arising after radiation therapy. | journal=Neurol Res | year= 2007 | volume= 29 | issue= 7 | pages= 723-6 | pmid=17553214 | doi=10.1179/016164107X208068 | pmc= | url=http://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=17553214  }} </ref><ref name="pmid1695334">{{cite journal| author=Ogasawara H, Kiya K, Uozumi T, Sugiyama K, Kawamoto K, Ohta M| title=Multiple oligodendroglioma--case report. | journal=Neurol Med Chir (Tokyo) | year= 1990 | volume= 30 | issue= 2 | pages= 127-31 | pmid=1695334 | doi= | pmc= | url=http://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=1695334  }} </ref><ref name="pmid2308753">{{cite journal| author=Raciti-Daurio C, Caruso J| title=Oligodendroglioma--a case presentation. | journal=Optom Vis Sci | year= 1990 | volume= 67 | issue= 1 | pages= 56-8 | pmid=2308753 | doi= | pmc= | url=http://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=2308753  }} </ref>


==History==
==History==

Revision as of 19:10, 14 October 2015

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Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]Associate Editor(s)-in-Chief: Sujit Routray, M.D. [2]

Overview

When evaluating a patient for oligodendroglioma, you should take a detailed history of the presenting symptom (onset, duration, and progression), other associated symptoms, and a thorough past medical history review. Other specific areas of focus when obtaining the history include review of common risk factors such as family history of brain tumors.[1] Symptoms associated with oligodendroglioma include seizure, headache, nausea, vomiting, vertigo, changes in speech, mood, and personality, visual loss, diplopia, strabismus, muscle weakness, and numbness.[2][3][4][5]

History

When evaluating a patient for oligodendroglioma, you should take a detailed history of the presenting symptom (onset, duration, and progression), other associated symptoms, and a thorough past medical history review. Other specific areas of focus when obtaining the history include:[1]

Symptoms

Common symptoms associated with oligodendroglioma include:[2][3][4][5]

References

  1. ↑ 1.0 1.1 McCarthy BJ, Rankin KM, Aldape K, Bondy ML, Brännström T, Broholm H; et al. (2011). "Risk factors for oligodendroglial tumors: a pooled international study". Neuro Oncol. 13 (2): 242–50. doi:10.1093/neuonc/noq173. PMC 3064625. PMID 21149253.
  2. ↑ 2.0 2.1 Douay X, Daems-Monpeurt C, Labalette P, Blond S, Petit H (1997). "[Bilateral 3rd cranial nerve palsy disclosing oligodendroglioma]". Rev Neurol (Paris). 153 (6–7): 430–2. PMID 9684012.
  3. ↑ 3.0 3.1 Hata N, Shono T, Mizoguchi M, Matsumoto K, Guan Y, Nagata S; et al. (2007). "Loss of heterozygosity analysis in an anaplastic oligodendroglioma arising after radiation therapy". Neurol Res. 29 (7): 723–6. doi:10.1179/016164107X208068. PMID 17553214.
  4. ↑ 4.0 4.1 Ogasawara H, Kiya K, Uozumi T, Sugiyama K, Kawamoto K, Ohta M (1990). "Multiple oligodendroglioma--case report". Neurol Med Chir (Tokyo). 30 (2): 127–31. PMID 1695334.
  5. ↑ 5.0 5.1 Raciti-Daurio C, Caruso J (1990). "Oligodendroglioma--a case presentation". Optom Vis Sci. 67 (1): 56–8. PMID 2308753.


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