Adrenal angiomyolipoma: A rare entity

Angiomyolipoma is apparently a part of a family of neoplasms that derive from perivascular epitheloid cells. It is a rare mesenchymal tumor, usually found in the kidney. Extrarenal angiomyolipoma is uncommon and the most common extrarenal site is the liver. Only two cases of adrenal angiomyolipoma a...

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Autores principales: Godara, Rajesh, Vashist, M. G., Singla, Sham L., Garg, Pradeep, Sen, Jyotsena, Mathur, S. K., Gupta, Anshu
Formato: Texto
Lenguaje:English
Publicado: Medknow Publications 2007
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2721616/
https://www.ncbi.nlm.nih.gov/pubmed/19718340
http://dx.doi.org/10.4103/0970-1591.33734
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author Godara, Rajesh
Vashist, M. G.
Singla, Sham L.
Garg, Pradeep
Sen, Jyotsena
Mathur, S. K.
Gupta, Anshu
author_facet Godara, Rajesh
Vashist, M. G.
Singla, Sham L.
Garg, Pradeep
Sen, Jyotsena
Mathur, S. K.
Gupta, Anshu
author_sort Godara, Rajesh
collection PubMed
description Angiomyolipoma is apparently a part of a family of neoplasms that derive from perivascular epitheloid cells. It is a rare mesenchymal tumor, usually found in the kidney. Extrarenal angiomyolipoma is uncommon and the most common extrarenal site is the liver. Only two cases of adrenal angiomyolipoma are reported in English literature. Authors wish to add one more case to world literature. Because of its large size and symptomatic presentation of extremely rare tumor merits documentation.
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spelling pubmed-27216162009-08-29 Adrenal angiomyolipoma: A rare entity Godara, Rajesh Vashist, M. G. Singla, Sham L. Garg, Pradeep Sen, Jyotsena Mathur, S. K. Gupta, Anshu Indian J Urol Case Report Angiomyolipoma is apparently a part of a family of neoplasms that derive from perivascular epitheloid cells. It is a rare mesenchymal tumor, usually found in the kidney. Extrarenal angiomyolipoma is uncommon and the most common extrarenal site is the liver. Only two cases of adrenal angiomyolipoma are reported in English literature. Authors wish to add one more case to world literature. Because of its large size and symptomatic presentation of extremely rare tumor merits documentation. Medknow Publications 2007 /pmc/articles/PMC2721616/ /pubmed/19718340 http://dx.doi.org/10.4103/0970-1591.33734 Text en © Indian Journal of Urology http://creativecommons.org/licenses/by/2.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Case Report
Godara, Rajesh
Vashist, M. G.
Singla, Sham L.
Garg, Pradeep
Sen, Jyotsena
Mathur, S. K.
Gupta, Anshu
Adrenal angiomyolipoma: A rare entity
title Adrenal angiomyolipoma: A rare entity
title_full Adrenal angiomyolipoma: A rare entity
title_fullStr Adrenal angiomyolipoma: A rare entity
title_full_unstemmed Adrenal angiomyolipoma: A rare entity
title_short Adrenal angiomyolipoma: A rare entity
title_sort adrenal angiomyolipoma: a rare entity
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2721616/
https://www.ncbi.nlm.nih.gov/pubmed/19718340
http://dx.doi.org/10.4103/0970-1591.33734
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AT gargpradeep adrenalangiomyolipomaarareentity
AT senjyotsena adrenalangiomyolipomaarareentity
AT mathursk adrenalangiomyolipomaarareentity
AT guptaanshu adrenalangiomyolipomaarareentity

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