Lipoma pathophysiology: Difference between revisions
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Lipoma is formed from mature adipocyte cells and is histologically indistinguishable from [[fat tissue]]. Recent studies have observed [[Cytogenetics|cytogenetic]] abnormalities in 50-60% of lipomas, suggesting its role in the lipoma [[pathogenesis]]. Rearrangements of [[chromosome 12]] are the most commonly [[Cytogenetics|cytogenetic]] abnormality. In a [[cross-sectional]] appearance, the lipoma is pale yellow to orange and has a uniform greasy surface with a lobular pattern. The [[subcutaneous]] lipoma is usually encapsulated and has a distinct lobulated [[pattern]]. | Lipoma is formed from mature adipocyte cells and is histologically indistinguishable from [[fat tissue]]. Recent studies have observed [[Cytogenetics|cytogenetic]] abnormalities in 50-60% of lipomas, suggesting its role in the lipoma [[pathogenesis]]. Rearrangements of [[chromosome 12]] are the most commonly [[Cytogenetics|cytogenetic]] abnormality. In a [[cross-sectional]] appearance, the lipoma is pale yellow to orange and has a uniform greasy surface with a lobular pattern. The [[subcutaneous]] lipoma is usually encapsulated and has a distinct lobulated [[pattern]]. | ||
==Pathophysiology== | ==Pathophysiology== | ||
*Lipoma is formed from mature [[adipocyte]]<nowiki/>s and is [[histologically]] indistinguishable from [[fat tissue]]. | *<nowiki/>Lipoma is formed from mature [[adipocyte]]<nowiki/>s and is [[histologically]] indistinguishable from [[fat tissue]]. | ||
*Recent studies have observed [[cytogenetic]] abnormalities in 50-60% of lipomas, suggesting its role in the lipoma [[pathogenesis]].<ref name="pmid1988102">{{cite journal |vauthors=Sreekantaiah C, Leong SP, Karakousis CP, McGee DL, Rappaport WD, Villar HV, Neal D, Fleming S, Wankel A, Herrington PN |title=Cytogenetic profile of 109 lipomas |journal=Cancer Res. |volume=51 |issue=1 |pages=422–33 |date=January 1991 |pmid=1988102 |doi= |url=}}</ref><ref name="pmid8744279">{{cite journal |vauthors=Weiss SW |title=Lipomatous tumors |journal=Monogr Pathol |volume=38 |issue= |pages=207–39 |date=1996 |pmid=8744279 |doi= |url=}}</ref> | *Recent studies have observed [[cytogenetic|cytogenet]]<nowiki/>[[cytogenetic|ic]] abnormalities in 50-60% of lipomas, suggesting its role in the lipoma [[pathogenesis]].<ref name="pmid1988102">{{cite journal |vauthors=Sreekantaiah C, Leong SP, Karakousis CP, McGee DL, Rappaport WD, Villar HV, Neal D, Fleming S, Wankel A, Herrington PN |title=Cytogenetic profile of 109 lipomas |journal=Cancer Res. |volume=51 |issue=1 |pages=422–33 |date=January 1991 |pmid=1988102 |doi= |url=}}</ref><ref name="pmid8744279">{{cite journal |vauthors=Weiss SW |title=Lipomatous tumors |journal=Monogr Pathol |volume=38 |issue= |pages=207–39 |date=1996 |pmid=8744279 |doi= |url=}}</ref> | ||
*Rearrangements of [[chromosome 12]] is the most commonly [[cytogenetic]] abnormality. | *Rearrangements of [[chromosome 12]] is the most commonly [[cytogenetic]] abnormality. | ||
*The [[DDIT3 gene|DDIT3]] [[gene]], located on the long arm of [[chromosome 12]], has been suggested to play a role in [[Adipocyte|adipocytic]] differentiation.<ref name="pmid9624148">{{cite journal |vauthors=Adelmant G, Gilbert JD, Freytag SO |title=Human translocation liposarcoma-CCAAT/enhancer binding protein (C/EBP) homologous protein (TLS-CHOP) oncoprotein prevents adipocyte differentiation by directly interfering with C/EBPbeta function |journal=J. Biol. Chem. |volume=273 |issue=25 |pages=15574–81 |date=June 1998 |pmid=9624148 |doi=10.1074/jbc.273.25.15574 |url=}}</ref> | *The [[DDIT3 gene|DDIT3]] [[gene]], located on the long arm of [[chromosome 12]], has been suggested to play a role in [[Adipocyte|adipocytic]] differentiation.<ref name="pmid9624148">{{cite journal |vauthors=Adelmant G, Gilbert JD, Freytag SO |title=Human translocation liposarcoma-CCAAT/enhancer binding protein (C/EBP) homologous protein (TLS-CHOP) oncoprotein prevents adipocyte differentiation by directly interfering with C/EBPbeta function |journal=J. Biol. Chem. |volume=273 |issue=25 |pages=15574–81 |date=June 1998 |pmid=9624148 |doi=10.1074/jbc.273.25.15574 |url=}}</ref> | ||
*This [[gene]] encodes a protein family, known to be enhancer binding [[protein]]. | *This [[gene]] encodes a protein family, known to be enhancer binding [[protein]]. | ||
*Members of this [[protein]] family are highly expressed in [[fat]] and are engaged in the growth arrest of [[fat cells]]. | *Members of this [[protein]] family are highly expressed in [[fat]] and are engaged in the [[growth]] arrest of [[fat cells]]. | ||
=== Genetics === | === Genetics === | ||
*[[Genetic]] abnormalities associated with lipoma [[pathogenesis]] include:<ref name="WillénÅkerman1998">{{cite journal|last1=Willén|first1=Helena|last2=Åkerman|first2=Måns|last3=Dal Cin|first3=Paola|last4=De Wever|first4=Ivo|last5=Fletcher|first5=Christopher D.M|last6=Mandahl|first6=Nils|last7=Mertens|first7=Fredrik|last8=Mitelman|first8=Felix|last9=Rosai|first9=Juan|last10=Rydholm|first10=Anders|last11=Sciot|first11=Raf|last12=Tallini|first12=Giovanni|last13=Van Den Berghe|first13=Herman|last14=Vanni|first14=Roberta|title=Comparison of Chromosomal Patterns with Clinical Features in 165 Lipomas: A Report of the CHAMP Study Group|journal=Cancer Genetics and Cytogenetics|volume=102|issue=1|year=1998|pages=46–49|issn=01654608|doi=10.1016/S0165-4608(97)00292-6}}</ref> | *[[Genetic]] abnormalities associated with lipoma [[pathogenesis]] include:<ref name="WillénÅkerman1998">{{cite journal|last1=Willén|first1=Helena|last2=Åkerman|first2=Måns|last3=Dal Cin|first3=Paola|last4=De Wever|first4=Ivo|last5=Fletcher|first5=Christopher D.M|last6=Mandahl|first6=Nils|last7=Mertens|first7=Fredrik|last8=Mitelman|first8=Felix|last9=Rosai|first9=Juan|last10=Rydholm|first10=Anders|last11=Sciot|first11=Raf|last12=Tallini|first12=Giovanni|last13=Van Den Berghe|first13=Herman|last14=Vanni|first14=Roberta|title=Comparison of Chromosomal Patterns with Clinical Features in 165 Lipomas: A Report of the CHAMP Study Group|journal=Cancer Genetics and Cytogenetics|volume=102|issue=1|year=1998|pages=46–49|issn=01654608|doi=10.1016/S0165-4608(97)00292-6}}</ref> | ||
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*Focal [[hemorrhage]] or [[fat necrosis]] may also occur, but it is much less common than in [[Liposarcoma|liposarcomas]]. | *Focal [[hemorrhage]] or [[fat necrosis]] may also occur, but it is much less common than in [[Liposarcoma|liposarcomas]]. | ||
*[[Intramuscular]] lipomas are usually larger than [[subcutaneous]] lipomas and may be encapsulated or diffuse.<ref>{{cite book | last = Miettinen | first = Markku | title = Modern soft tissue pathology : tumors and non-neoplastic conditions | publisher = Cambridge University Press | location = Cambridge New York | year = 2010 | isbn = 9780521874090 }}</ref> | *[[Intramuscular]] lipomas are usually larger than [[subcutaneous]] lipomas and may be encapsulated or diffuse.<ref>{{cite book | last = Miettinen | first = Markku | title = Modern soft tissue pathology : tumors and non-neoplastic conditions | publisher = Cambridge University Press | location = Cambridge New York | year = 2010 | isbn = 9780521874090 }}</ref> | ||
*Grayish streaks of fibrous tissue may also be seen in fibrolipoma which has a firmer texture compared to ordinary lipoma. | *Grayish streaks of [[fibrous tissue]] may also be seen in fibrolipoma which has a firmer texture compared to ordinary lipoma. | ||
[[File:Lipoma 06.jpg|thumb|none|400px|Lipoma gross appearance<ref>Image courtesy of Sebastian E Valbuena, Greg A O'Toole and Eric Roulot, wikimedia commons</ref>]] | [[File:Lipoma 06.jpg|thumb|none|400px|Lipoma gross appearance<ref>Image courtesy of Sebastian E Valbuena, Greg A O'Toole and Eric Roulot, wikimedia commons</ref>]] | ||
=== Microscopic pathology === | === Microscopic pathology === | ||
*[[Microscopic|Microscopically]], lipomas are formed from mature [[fat cells]].<ref name="SimangoRamdial2000">{{cite journal|last1=Simango|first1=Stephen|last2=Ramdial|first2=Pratistadevi K.|last3=Madaree|first3=Anil|title=Subpectoral post-traumatic lipoma|journal=British Journal of Plastic Surgery|volume=53|issue=7|year=2000|pages=627–629|issn=00071226|doi=10.1054/bjps.2000.3396}}</ref> | *[[Microscopic|Microscopically]], lipomas are formed from mature [[fat cells]].<ref name="SimangoRamdial2000">{{cite journal|last1=Simango|first1=Stephen|last2=Ramdial|first2=Pratistadevi K.|last3=Madaree|first3=Anil|title=Subpectoral post-traumatic lipoma|journal=British Journal of Plastic Surgery|volume=53|issue=7|year=2000|pages=627–629|issn=00071226|doi=10.1054/bjps.2000.3396}}</ref> | ||
*There is no [[nuclear]] hyperchromasia. | *There is no [[nuclear]] hyperchromasia. | ||
*Subcutaneous lipoma is usually encapsulated and have a distinct lobulated [[pattern]]. | *[[Subcutaneous]] lipoma is usually encapsulated and have a distinct lobulated [[pattern]]. | ||
*Cystic like changes may also be seen in lipoma due to impaired blood supply. | *[[Cystic]] like changes may also be seen in lipoma due to impaired [[blood]] supply. | ||
*Infection or trauma may cause fat necrosis or local liquefaction of fat, which may appear with phagocytic cells and formation of lipid cysts. | *[[Infection]] or [[trauma]] may cause [[fat necrosis]] or local liquefaction of fat, which may appear with [[phagocytic]] cells and formation of lipid [[cysts]]. | ||
*A possible benign finding in lipoma is the collection of histiocytes and the vacuolization of the | *A possible [[benign]] finding in lipoma is the collection of [[histiocytes]] and the [[vacuolization]] of the [[nucleus]].<ref>{{cite book | last = Miettinen | first = Markku | title = Modern soft tissue pathology : tumors and non-neoplastic conditions | publisher = Cambridge University Press | location = Cambridge New York | year = 2010 | isbn = 9780521874090 }}</ref> | ||
*[[Intramuscular]] lipoma may be well-demarcated from the adjacent muscular tissue or have a diffuse pattern with alternating adipocytes and skeletal muscle cells. | *[[Intramuscular]] lipoma may be well-demarcated from the adjacent [[muscular tissue]] or have a diffuse [[pattern]] with alternating [[adipocytes]] and [[skeletal muscle]] cells. | ||
[[File:Spindle cell lipoma -- intermed mag.jpg|thumb|left|200px|Histologic view of spindle cell lipoma<ref>wikimedia commons</ref>]] | [[File:Spindle cell lipoma -- intermed mag.jpg|thumb|left|200px|Histologic view of spindle cell lipoma<ref>wikimedia commons</ref>]] | ||
[[File:Spindle Cell Lipoma (2275051876).jpg|thumb|center|400px|Histologic view of subcutaneous lipoma<ref>Pathological and histological images courtesy of Ed Uthman at flickr, wikimedia commons</ref>]] | [[File:Spindle Cell Lipoma (2275051876).jpg|thumb|center|400px|Histologic view of subcutaneous lipoma<ref>Pathological and histological images courtesy of Ed Uthman at flickr, wikimedia commons</ref>]] |
Latest revision as of 18:13, 21 November 2019
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Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1] Associate Editor(s)-in-Chief: Sahar Memar Montazerin, M.D.[2]
Overview
Lipoma is formed from mature adipocyte cells and is histologically indistinguishable from fat tissue. Recent studies have observed cytogenetic abnormalities in 50-60% of lipomas, suggesting its role in the lipoma pathogenesis. Rearrangements of chromosome 12 are the most commonly cytogenetic abnormality. In a cross-sectional appearance, the lipoma is pale yellow to orange and has a uniform greasy surface with a lobular pattern. The subcutaneous lipoma is usually encapsulated and has a distinct lobulated pattern.
Pathophysiology
- Lipoma is formed from mature adipocytes and is histologically indistinguishable from fat tissue.
- Recent studies have observed cytogenetic abnormalities in 50-60% of lipomas, suggesting its role in the lipoma pathogenesis.[1][2]
- Rearrangements of chromosome 12 is the most commonly cytogenetic abnormality.
- The DDIT3 gene, located on the long arm of chromosome 12, has been suggested to play a role in adipocytic differentiation.[3]
- This gene encodes a protein family, known to be enhancer binding protein.
- Members of this protein family are highly expressed in fat and are engaged in the growth arrest of fat cells.
Genetics
- Genetic abnormalities associated with lipoma pathogenesis include:[4]
- Translocations in 12q13-15
- Interstitial deletions of 13q
- Rearrangements in 6p21-23
Gross pathology
- Gross pathology of lipoma may differ depending on anatomical location.[5]
- Subcutaneous lipoma appear as a a soft, well-circumscribed rounded mass with different size ranging from millimeters to 5 cm or more.
- Lipomas larger than 10 cm are not common.
- In cross-sectional appearance, the lipoma is pale yellow to orange and has a uniform greasy surface with a lobular pattern.
- Lipoma is usually encapsulated.
- Focal hemorrhage or fat necrosis may also occur, but it is much less common than in liposarcomas.
- Intramuscular lipomas are usually larger than subcutaneous lipomas and may be encapsulated or diffuse.[6]
- Grayish streaks of fibrous tissue may also be seen in fibrolipoma which has a firmer texture compared to ordinary lipoma.
Microscopic pathology
- Microscopically, lipomas are formed from mature fat cells.[8]
- There is no nuclear hyperchromasia.
- Subcutaneous lipoma is usually encapsulated and have a distinct lobulated pattern.
- Cystic like changes may also be seen in lipoma due to impaired blood supply.
- Infection or trauma may cause fat necrosis or local liquefaction of fat, which may appear with phagocytic cells and formation of lipid cysts.
- A possible benign finding in lipoma is the collection of histiocytes and the vacuolization of the nucleus.[9]
- Intramuscular lipoma may be well-demarcated from the adjacent muscular tissue or have a diffuse pattern with alternating adipocytes and skeletal muscle cells.
Immunohistochemistry
- Lipomas may have following immunohistochemical markers:[12]
Gallery
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Histopathologic slide of renal angiomyolipoma. Nephrectomy specimen. H & E stain.[13]
-
Histopathologic slide of renal angiomyolipoma. Nephrectomy specimen. H & E stain.[13]
-
Histopathologic slide of renal angiomyolipoma. Nephrectomy specimen. H & E stain.[13]
-
Histopathologic image of renal angiomyolipoma. Nephrectomy specimen. HMB-45 immunostain.[13]
References
- ↑ Sreekantaiah C, Leong SP, Karakousis CP, McGee DL, Rappaport WD, Villar HV, Neal D, Fleming S, Wankel A, Herrington PN (January 1991). "Cytogenetic profile of 109 lipomas". Cancer Res. 51 (1): 422–33. PMID 1988102.
- ↑ Weiss SW (1996). "Lipomatous tumors". Monogr Pathol. 38: 207–39. PMID 8744279.
- ↑ Adelmant G, Gilbert JD, Freytag SO (June 1998). "Human translocation liposarcoma-CCAAT/enhancer binding protein (C/EBP) homologous protein (TLS-CHOP) oncoprotein prevents adipocyte differentiation by directly interfering with C/EBPbeta function". J. Biol. Chem. 273 (25): 15574–81. doi:10.1074/jbc.273.25.15574. PMID 9624148.
- ↑ Willén, Helena; Åkerman, Måns; Dal Cin, Paola; De Wever, Ivo; Fletcher, Christopher D.M; Mandahl, Nils; Mertens, Fredrik; Mitelman, Felix; Rosai, Juan; Rydholm, Anders; Sciot, Raf; Tallini, Giovanni; Van Den Berghe, Herman; Vanni, Roberta (1998). "Comparison of Chromosomal Patterns with Clinical Features in 165 Lipomas: A Report of the CHAMP Study Group". Cancer Genetics and Cytogenetics. 102 (1): 46–49. doi:10.1016/S0165-4608(97)00292-6. ISSN 0165-4608.
- ↑ Miettinen, Markku (2010). Modern soft tissue pathology : tumors and non-neoplastic conditions. Cambridge New York: Cambridge University Press. ISBN 9780521874090.
- ↑ Miettinen, Markku (2010). Modern soft tissue pathology : tumors and non-neoplastic conditions. Cambridge New York: Cambridge University Press. ISBN 9780521874090.
- ↑ Image courtesy of Sebastian E Valbuena, Greg A O'Toole and Eric Roulot, wikimedia commons
- ↑ Simango, Stephen; Ramdial, Pratistadevi K.; Madaree, Anil (2000). "Subpectoral post-traumatic lipoma". British Journal of Plastic Surgery. 53 (7): 627–629. doi:10.1054/bjps.2000.3396. ISSN 0007-1226.
- ↑ Miettinen, Markku (2010). Modern soft tissue pathology : tumors and non-neoplastic conditions. Cambridge New York: Cambridge University Press. ISBN 9780521874090.
- ↑ wikimedia commons
- ↑ Pathological and histological images courtesy of Ed Uthman at flickr, wikimedia commons
- ↑ Fletcher, Christopher (2002). Pathology and genetics of tumours of soft tissue and bone. Lyon: IARC Press. ISBN 9283224132.
- ↑ 13.0 13.1 13.2 13.3 http://librepathology.org/wiki/index.php/Angiomyolipoma