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Malignant Subcutaneous Perivascular Epithelioid Cell Tumor of Anterior Abdominal Wall

Perivascular epithelioid cell tumors (PEComas) are a family of rare mesenchymal tumors with discrete histological and immunohistochemical characteristics. Even rarer among them are cutaneous and subcutaneous PEComas. We describe a 34-year-old woman who presented with a large anterior abdominal subcu...

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Autores principales: Gan, David Eng Yeow, Choy, Rebecca Xin Yi, Sellappan, Harivinthan, Hayati, Firdaus, Azizan, Nornazirah
Formato: Online Artículo Texto
Lenguaje:English
Publicado: OMJ 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7988466/
https://www.ncbi.nlm.nih.gov/pubmed/33768970
http://dx.doi.org/10.5001/omj.2021.21
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author Gan, David Eng Yeow
Choy, Rebecca Xin Yi
Sellappan, Harivinthan
Hayati, Firdaus
Azizan, Nornazirah
author_facet Gan, David Eng Yeow
Choy, Rebecca Xin Yi
Sellappan, Harivinthan
Hayati, Firdaus
Azizan, Nornazirah
author_sort Gan, David Eng Yeow
collection PubMed
description Perivascular epithelioid cell tumors (PEComas) are a family of rare mesenchymal tumors with discrete histological and immunohistochemical characteristics. Even rarer among them are cutaneous and subcutaneous PEComas. We describe a 34-year-old woman who presented with a large anterior abdominal subcutaneous lesion showing intact overlying skin and no obvious invasion of the abdominal musculature. A wide local excision was performed. Histopathology revealed a solitary tumor measuring 75 × 55 × 90 mm with epithelioid cells in nests with thin fibrovascular septa and spindle cells. Resection margins were clear with no invasion to the skin or rectus sheath. Tumor cells were positive for HMB-45 but negative for other markers. This is the largest subcutaneous PEComa reported to date.
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spelling pubmed-79884662021-03-24 Malignant Subcutaneous Perivascular Epithelioid Cell Tumor of Anterior Abdominal Wall Gan, David Eng Yeow Choy, Rebecca Xin Yi Sellappan, Harivinthan Hayati, Firdaus Azizan, Nornazirah Oman Med J Case Report Perivascular epithelioid cell tumors (PEComas) are a family of rare mesenchymal tumors with discrete histological and immunohistochemical characteristics. Even rarer among them are cutaneous and subcutaneous PEComas. We describe a 34-year-old woman who presented with a large anterior abdominal subcutaneous lesion showing intact overlying skin and no obvious invasion of the abdominal musculature. A wide local excision was performed. Histopathology revealed a solitary tumor measuring 75 × 55 × 90 mm with epithelioid cells in nests with thin fibrovascular septa and spindle cells. Resection margins were clear with no invasion to the skin or rectus sheath. Tumor cells were positive for HMB-45 but negative for other markers. This is the largest subcutaneous PEComa reported to date. OMJ 2021-03-23 /pmc/articles/PMC7988466/ /pubmed/33768970 http://dx.doi.org/10.5001/omj.2021.21 Text en The OMJ is Published Bimonthly and Copyrighted 2021 by the OMSB. This is an open-access article distributed under the terms of the Creative Commons Attribution Non-Commercial (CC BY-NC) 4.0 License. http://creativecommons.org/licenses/by-nc/4.0/
spellingShingle Case Report
Gan, David Eng Yeow
Choy, Rebecca Xin Yi
Sellappan, Harivinthan
Hayati, Firdaus
Azizan, Nornazirah
Malignant Subcutaneous Perivascular Epithelioid Cell Tumor of Anterior Abdominal Wall
title Malignant Subcutaneous Perivascular Epithelioid Cell Tumor of Anterior Abdominal Wall
title_full Malignant Subcutaneous Perivascular Epithelioid Cell Tumor of Anterior Abdominal Wall
title_fullStr Malignant Subcutaneous Perivascular Epithelioid Cell Tumor of Anterior Abdominal Wall
title_full_unstemmed Malignant Subcutaneous Perivascular Epithelioid Cell Tumor of Anterior Abdominal Wall
title_short Malignant Subcutaneous Perivascular Epithelioid Cell Tumor of Anterior Abdominal Wall
title_sort malignant subcutaneous perivascular epithelioid cell tumor of anterior abdominal wall
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7988466/
https://www.ncbi.nlm.nih.gov/pubmed/33768970
http://dx.doi.org/10.5001/omj.2021.21
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