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Anastomosing hemangioma: A case report of a benign tumor often misdiagnosed as a malignant epithelioid angiosarcoma

Anastomosing hemangioma (AH), a rare benign genitourinary tract hemangioma is subject to frequent misdiagnosis due to its rarity and clinical, histological, and immunohistochemical similarities it shares with several diagnoses, including well-differentiated angiosarcoma (AS). This is particularly tr...

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Detalles Bibliográficos
Autores principales: Shaker, Nada, Patel, Ankush, Tozbikian, Gary, Parwani, Anil
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9073214/
https://www.ncbi.nlm.nih.gov/pubmed/35530542
http://dx.doi.org/10.1016/j.eucr.2022.102023
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author Shaker, Nada
Patel, Ankush
Tozbikian, Gary
Parwani, Anil
author_facet Shaker, Nada
Patel, Ankush
Tozbikian, Gary
Parwani, Anil
author_sort Shaker, Nada
collection PubMed
description Anastomosing hemangioma (AH), a rare benign genitourinary tract hemangioma is subject to frequent misdiagnosis due to its rarity and clinical, histological, and immunohistochemical similarities it shares with several diagnoses, including well-differentiated angiosarcoma (AS). This is particularly true of angiosarcoma, nearly identical to AH when presented in tissue samples of limited size. Lack of specific clinical and radiologic manifestations on initial preoperative assessment, coupled with limited diagnostic experience or awareness, can lead to misinterpretation of this entity, potentially leading to unnecessary clinical management. We present an initial misdiagnosis of AS which, upon review of the entire lesion, was identified as AH.
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spelling pubmed-90732142022-05-07 Anastomosing hemangioma: A case report of a benign tumor often misdiagnosed as a malignant epithelioid angiosarcoma Shaker, Nada Patel, Ankush Tozbikian, Gary Parwani, Anil Urol Case Rep Oncology Anastomosing hemangioma (AH), a rare benign genitourinary tract hemangioma is subject to frequent misdiagnosis due to its rarity and clinical, histological, and immunohistochemical similarities it shares with several diagnoses, including well-differentiated angiosarcoma (AS). This is particularly true of angiosarcoma, nearly identical to AH when presented in tissue samples of limited size. Lack of specific clinical and radiologic manifestations on initial preoperative assessment, coupled with limited diagnostic experience or awareness, can lead to misinterpretation of this entity, potentially leading to unnecessary clinical management. We present an initial misdiagnosis of AS which, upon review of the entire lesion, was identified as AH. Elsevier 2022-02-02 /pmc/articles/PMC9073214/ /pubmed/35530542 http://dx.doi.org/10.1016/j.eucr.2022.102023 Text en © 2022 Published by Elsevier Inc. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Oncology
Shaker, Nada
Patel, Ankush
Tozbikian, Gary
Parwani, Anil
Anastomosing hemangioma: A case report of a benign tumor often misdiagnosed as a malignant epithelioid angiosarcoma
title Anastomosing hemangioma: A case report of a benign tumor often misdiagnosed as a malignant epithelioid angiosarcoma
title_full Anastomosing hemangioma: A case report of a benign tumor often misdiagnosed as a malignant epithelioid angiosarcoma
title_fullStr Anastomosing hemangioma: A case report of a benign tumor often misdiagnosed as a malignant epithelioid angiosarcoma
title_full_unstemmed Anastomosing hemangioma: A case report of a benign tumor often misdiagnosed as a malignant epithelioid angiosarcoma
title_short Anastomosing hemangioma: A case report of a benign tumor often misdiagnosed as a malignant epithelioid angiosarcoma
title_sort anastomosing hemangioma: a case report of a benign tumor often misdiagnosed as a malignant epithelioid angiosarcoma
topic Oncology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9073214/
https://www.ncbi.nlm.nih.gov/pubmed/35530542
http://dx.doi.org/10.1016/j.eucr.2022.102023
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