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Primary Renal Epithelioid Hemangioendothelioma

Epithelioid hemangioendothelioma is a rare vascular tumor with intermediate biologic behavior and metastatic potential. Primary renal epithelioid hemangioendothelioma is extremely rare and we present the second report of this rare tumor in an interesting clinical scenario. A 59-year-old male with es...

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Detalles Bibliográficos
Autores principales: Roy, S., Parwani, A. V.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3485863/
https://www.ncbi.nlm.nih.gov/pubmed/23133773
http://dx.doi.org/10.1155/2012/802515
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author Roy, S.
Parwani, A. V.
author_facet Roy, S.
Parwani, A. V.
author_sort Roy, S.
collection PubMed
description Epithelioid hemangioendothelioma is a rare vascular tumor with intermediate biologic behavior and metastatic potential. Primary renal epithelioid hemangioendothelioma is extremely rare and we present the second report of this rare tumor in an interesting clinical scenario. A 59-year-old male with established history of widely metastatic high grade esophageal adenocarcinoma was found to have an isolated renal nodule on a followup computed tomography (CT) scan. Surgical excision, with the suspicion of metastatic carcinoma, and subsequent pathologic examination revealed an epithelioid hemangioendothelioma. The various differential diagnoses and use of morphological clues and immunohistochemistry are discussed.
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spelling pubmed-34858632012-11-06 Primary Renal Epithelioid Hemangioendothelioma Roy, S. Parwani, A. V. Case Rep Pathol Case Report Epithelioid hemangioendothelioma is a rare vascular tumor with intermediate biologic behavior and metastatic potential. Primary renal epithelioid hemangioendothelioma is extremely rare and we present the second report of this rare tumor in an interesting clinical scenario. A 59-year-old male with established history of widely metastatic high grade esophageal adenocarcinoma was found to have an isolated renal nodule on a followup computed tomography (CT) scan. Surgical excision, with the suspicion of metastatic carcinoma, and subsequent pathologic examination revealed an epithelioid hemangioendothelioma. The various differential diagnoses and use of morphological clues and immunohistochemistry are discussed. Hindawi Publishing Corporation 2012 2012-10-24 /pmc/articles/PMC3485863/ /pubmed/23133773 http://dx.doi.org/10.1155/2012/802515 Text en Copyright © 2012 S. Roy and A. V. Parwani. https://creativecommons.org/licenses/by/3.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Case Report
Roy, S.
Parwani, A. V.
Primary Renal Epithelioid Hemangioendothelioma
title Primary Renal Epithelioid Hemangioendothelioma
title_full Primary Renal Epithelioid Hemangioendothelioma
title_fullStr Primary Renal Epithelioid Hemangioendothelioma
title_full_unstemmed Primary Renal Epithelioid Hemangioendothelioma
title_short Primary Renal Epithelioid Hemangioendothelioma
title_sort primary renal epithelioid hemangioendothelioma
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3485863/
https://www.ncbi.nlm.nih.gov/pubmed/23133773
http://dx.doi.org/10.1155/2012/802515
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