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Ankle Myopericytoma: A Rare Case Report and Cytogenetic Study

Myopericytoma (MPC) is an uncommon benign neoplasm of the skin and soft tissues belonging to a spectrum of tumors that are histologically recognized by their distinctive perivascular myoid cell differentiation. These distinct tumors are more prevalent among middle-aged males, and they arise more fre...

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Autores principales: Alqassab, Aqilah T, Alsadah, Fatimah Z, Elsharkawy, Tarek, Alhamad, Mohammad, Alsayed, Hassan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cureus 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8849462/
https://www.ncbi.nlm.nih.gov/pubmed/35186568
http://dx.doi.org/10.7759/cureus.21307
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author Alqassab, Aqilah T
Alsadah, Fatimah Z
Elsharkawy, Tarek
Alhamad, Mohammad
Alsayed, Hassan
author_facet Alqassab, Aqilah T
Alsadah, Fatimah Z
Elsharkawy, Tarek
Alhamad, Mohammad
Alsayed, Hassan
author_sort Alqassab, Aqilah T
collection PubMed
description Myopericytoma (MPC) is an uncommon benign neoplasm of the skin and soft tissues belonging to a spectrum of tumors that are histologically recognized by their distinctive perivascular myoid cell differentiation. These distinct tumors are more prevalent among middle-aged males, and they arise more frequently in the subcutaneous tissue of the four extremities. In this paper, myopericytoma is reported in a 59-year-old Saudi male, presented with a painless small cyst involving the left ankle suspected clinically to be a ganglion cyst. Following surgical excision of the cyst, the diagnosis of myopericytoma was made based on the histopathological pattern of the disease. This paper focuses on the clinical and histopathological findings of myopericytoma and emphasizes the importance of immunohistochemistry as well as molecular testing in reaching the final diagnosis.
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spelling pubmed-88494622022-02-18 Ankle Myopericytoma: A Rare Case Report and Cytogenetic Study Alqassab, Aqilah T Alsadah, Fatimah Z Elsharkawy, Tarek Alhamad, Mohammad Alsayed, Hassan Cureus Pathology Myopericytoma (MPC) is an uncommon benign neoplasm of the skin and soft tissues belonging to a spectrum of tumors that are histologically recognized by their distinctive perivascular myoid cell differentiation. These distinct tumors are more prevalent among middle-aged males, and they arise more frequently in the subcutaneous tissue of the four extremities. In this paper, myopericytoma is reported in a 59-year-old Saudi male, presented with a painless small cyst involving the left ankle suspected clinically to be a ganglion cyst. Following surgical excision of the cyst, the diagnosis of myopericytoma was made based on the histopathological pattern of the disease. This paper focuses on the clinical and histopathological findings of myopericytoma and emphasizes the importance of immunohistochemistry as well as molecular testing in reaching the final diagnosis. Cureus 2022-01-17 /pmc/articles/PMC8849462/ /pubmed/35186568 http://dx.doi.org/10.7759/cureus.21307 Text en Copyright © 2022, Alqassab et al. https://creativecommons.org/licenses/by/3.0/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 author and source are credited.
spellingShingle Pathology
Alqassab, Aqilah T
Alsadah, Fatimah Z
Elsharkawy, Tarek
Alhamad, Mohammad
Alsayed, Hassan
Ankle Myopericytoma: A Rare Case Report and Cytogenetic Study
title Ankle Myopericytoma: A Rare Case Report and Cytogenetic Study
title_full Ankle Myopericytoma: A Rare Case Report and Cytogenetic Study
title_fullStr Ankle Myopericytoma: A Rare Case Report and Cytogenetic Study
title_full_unstemmed Ankle Myopericytoma: A Rare Case Report and Cytogenetic Study
title_short Ankle Myopericytoma: A Rare Case Report and Cytogenetic Study
title_sort ankle myopericytoma: a rare case report and cytogenetic study
topic Pathology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8849462/
https://www.ncbi.nlm.nih.gov/pubmed/35186568
http://dx.doi.org/10.7759/cureus.21307
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