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Metastatic perivascular epithelioid cell tumor responding to mammalian target of rapamycin inhibition

Perivascular epithelioid cell tumors (PEComa) are a family of rare mesenchymal tumors composed of histologically and immunohistochemically distinctive perivascular epithelioid cells. Female genital tract and retroperitoneum are common sites of origin of PEComa-not otherwise specified. Diagnosis depe...

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Autores principales: Ghosh, Indranil, Arun, Indu, Sen, Saugata, Mishra, Lopamudra
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Medknow Publications & Media Pvt Ltd 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4080675/
https://www.ncbi.nlm.nih.gov/pubmed/25006296
http://dx.doi.org/10.4103/0971-5851.133733
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author Ghosh, Indranil
Arun, Indu
Sen, Saugata
Mishra, Lopamudra
author_facet Ghosh, Indranil
Arun, Indu
Sen, Saugata
Mishra, Lopamudra
author_sort Ghosh, Indranil
collection PubMed
description Perivascular epithelioid cell tumors (PEComa) are a family of rare mesenchymal tumors composed of histologically and immunohistochemically distinctive perivascular epithelioid cells. Female genital tract and retroperitoneum are common sites of origin of PEComa-not otherwise specified. Diagnosis depends upon characteristic morphology and immunohistochemistry findings. Prognosis of unresectable or metastatic disease is poor. Responses to mammalian target of rapamycin (mTOR) inhibition are encouraging but mostly short-lived. We report a case of metastatic PEComa who responded to mTOR inhibition, albeit for a short duration. We also review the existing literature on mTOR inhibitors in PEComa.
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spelling pubmed-40806752014-07-08 Metastatic perivascular epithelioid cell tumor responding to mammalian target of rapamycin inhibition Ghosh, Indranil Arun, Indu Sen, Saugata Mishra, Lopamudra Indian J Med Paediatr Oncol Case Report Perivascular epithelioid cell tumors (PEComa) are a family of rare mesenchymal tumors composed of histologically and immunohistochemically distinctive perivascular epithelioid cells. Female genital tract and retroperitoneum are common sites of origin of PEComa-not otherwise specified. Diagnosis depends upon characteristic morphology and immunohistochemistry findings. Prognosis of unresectable or metastatic disease is poor. Responses to mammalian target of rapamycin (mTOR) inhibition are encouraging but mostly short-lived. We report a case of metastatic PEComa who responded to mTOR inhibition, albeit for a short duration. We also review the existing literature on mTOR inhibitors in PEComa. Medknow Publications & Media Pvt Ltd 2014 /pmc/articles/PMC4080675/ /pubmed/25006296 http://dx.doi.org/10.4103/0971-5851.133733 Text en Copyright: © Indian Journal of Medical and Paediatric Oncology http://creativecommons.org/licenses/by-nc-sa/3.0 This is an open-access article distributed under the terms of the Creative Commons Attribution-Noncommercial-Share Alike 3.0 Unported, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Case Report
Ghosh, Indranil
Arun, Indu
Sen, Saugata
Mishra, Lopamudra
Metastatic perivascular epithelioid cell tumor responding to mammalian target of rapamycin inhibition
title Metastatic perivascular epithelioid cell tumor responding to mammalian target of rapamycin inhibition
title_full Metastatic perivascular epithelioid cell tumor responding to mammalian target of rapamycin inhibition
title_fullStr Metastatic perivascular epithelioid cell tumor responding to mammalian target of rapamycin inhibition
title_full_unstemmed Metastatic perivascular epithelioid cell tumor responding to mammalian target of rapamycin inhibition
title_short Metastatic perivascular epithelioid cell tumor responding to mammalian target of rapamycin inhibition
title_sort metastatic perivascular epithelioid cell tumor responding to mammalian target of rapamycin inhibition
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4080675/
https://www.ncbi.nlm.nih.gov/pubmed/25006296
http://dx.doi.org/10.4103/0971-5851.133733
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