Incidental Primary Angiomyolipoma of Ovary: A Rare Case Report and Literature Review

ABSTRACT Primary angiomyolipomas of the ovary which are not associated with genetical systemic diseases, particularly tuberous sclerosis, are extremely rare and are more likely to pose diagnostic challenges. This tumor, particularly of epithelioid variant, is more likely to be malignant and can carr...

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Main Authors: James J. Yahaya, Emmanuel D. Morgan, Veronica Nyakato, Emmanuel Othieno
Format: Article
Language:English
Published: Wiley 2025-03-01
Series:Clinical Case Reports
Subjects:
Online Access:https://doi.org/10.1002/ccr3.70278
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author James J. Yahaya
Emmanuel D. Morgan
Veronica Nyakato
Emmanuel Othieno
author_facet James J. Yahaya
Emmanuel D. Morgan
Veronica Nyakato
Emmanuel Othieno
author_sort James J. Yahaya
collection DOAJ
description ABSTRACT Primary angiomyolipomas of the ovary which are not associated with genetical systemic diseases, particularly tuberous sclerosis, are extremely rare and are more likely to pose diagnostic challenges. This tumor, particularly of epithelioid variant, is more likely to be malignant and can carry a high possibility of metastasizing. Use of immunohistochemistry consisting of melanocytic biomarkers (HMB45 and Melan A) helps to ascertain their presence.
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spelling doaj-art-a573341a892f47a1b982d6f5c9016b952025-08-20T02:50:55ZengWileyClinical Case Reports2050-09042025-03-01133n/an/a10.1002/ccr3.70278Incidental Primary Angiomyolipoma of Ovary: A Rare Case Report and Literature ReviewJames J. Yahaya0Emmanuel D. Morgan1Veronica Nyakato2Emmanuel Othieno3Department of Pathology, School of Health Science Soroti University Soroti UgandaDepartment of Pathology, School of Health Science Soroti University Soroti UgandaDepartment of Pathology Uganda Cancer Institute (UCI) Kampala UgandaDepartment of Pathology, School of Health Science Soroti University Soroti UgandaABSTRACT Primary angiomyolipomas of the ovary which are not associated with genetical systemic diseases, particularly tuberous sclerosis, are extremely rare and are more likely to pose diagnostic challenges. This tumor, particularly of epithelioid variant, is more likely to be malignant and can carry a high possibility of metastasizing. Use of immunohistochemistry consisting of melanocytic biomarkers (HMB45 and Melan A) helps to ascertain their presence.https://doi.org/10.1002/ccr3.70278angiomyolipomaincidentalmesenchymal tumorovary
spellingShingle James J. Yahaya
Emmanuel D. Morgan
Veronica Nyakato
Emmanuel Othieno
Incidental Primary Angiomyolipoma of Ovary: A Rare Case Report and Literature Review
Clinical Case Reports
angiomyolipoma
incidental
mesenchymal tumor
ovary
title Incidental Primary Angiomyolipoma of Ovary: A Rare Case Report and Literature Review
title_full Incidental Primary Angiomyolipoma of Ovary: A Rare Case Report and Literature Review
title_fullStr Incidental Primary Angiomyolipoma of Ovary: A Rare Case Report and Literature Review
title_full_unstemmed Incidental Primary Angiomyolipoma of Ovary: A Rare Case Report and Literature Review
title_short Incidental Primary Angiomyolipoma of Ovary: A Rare Case Report and Literature Review
title_sort incidental primary angiomyolipoma of ovary a rare case report and literature review
topic angiomyolipoma
incidental
mesenchymal tumor
ovary
url https://doi.org/10.1002/ccr3.70278
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AT emmanuelothieno incidentalprimaryangiomyolipomaofovaryararecasereportandliteraturereview