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Intravascular papillary endothelial hyperplasia of the bladder: Case report and review of the literature

Intravascular papillary endothelial hyperplasia (IPEH), also known as Masson's tumor, is a benign unusual vascular lesion thought to arise from an organizing thrombus. Histologically, IPEH is characterized by papillary fronds lined by proliferating endothelium that may mimic angiosarcoma, and t...

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Autores principales: Jazaerly, Tarek, Jaratli, Hayan, Sakr, Wael, Almardini, Nour, Urabi, Muaz, Dhar, Nivedita, Giorgadze, Tamar
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Medknow Publications & Media Pvt Ltd 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3507062/
https://www.ncbi.nlm.nih.gov/pubmed/23210010
http://dx.doi.org/10.4103/2231-0770.90917
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author Jazaerly, Tarek
Jaratli, Hayan
Sakr, Wael
Almardini, Nour
Urabi, Muaz
Dhar, Nivedita
Giorgadze, Tamar
author_facet Jazaerly, Tarek
Jaratli, Hayan
Sakr, Wael
Almardini, Nour
Urabi, Muaz
Dhar, Nivedita
Giorgadze, Tamar
author_sort Jazaerly, Tarek
collection PubMed
description Intravascular papillary endothelial hyperplasia (IPEH), also known as Masson's tumor, is a benign unusual vascular lesion thought to arise from an organizing thrombus. Histologically, IPEH is characterized by papillary fronds lined by proliferating endothelium that may mimic angiosarcoma, and therefore the correct diagnosis may prevent unnecessary radical procedures. Involvement of the bladder is extremely rare, with only three cases reported in the literature. We report a case of IPEH arising in the bladder of a patient with history of prostate cancer treated with radiotherapy.
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spelling pubmed-35070622012-12-03 Intravascular papillary endothelial hyperplasia of the bladder: Case report and review of the literature Jazaerly, Tarek Jaratli, Hayan Sakr, Wael Almardini, Nour Urabi, Muaz Dhar, Nivedita Giorgadze, Tamar Avicenna J Med Case Report Intravascular papillary endothelial hyperplasia (IPEH), also known as Masson's tumor, is a benign unusual vascular lesion thought to arise from an organizing thrombus. Histologically, IPEH is characterized by papillary fronds lined by proliferating endothelium that may mimic angiosarcoma, and therefore the correct diagnosis may prevent unnecessary radical procedures. Involvement of the bladder is extremely rare, with only three cases reported in the literature. We report a case of IPEH arising in the bladder of a patient with history of prostate cancer treated with radiotherapy. Medknow Publications & Media Pvt Ltd 2011 /pmc/articles/PMC3507062/ /pubmed/23210010 http://dx.doi.org/10.4103/2231-0770.90917 Text en Copyright: © Avicenna Journal of Medicine http://creativecommons.org/licenses/by-nc-sa/3.0 This is an open-access article distributed under the terms of the Creative Commons Attribution-Noncommercial-Share Alike 3.0 Unported, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Case Report
Jazaerly, Tarek
Jaratli, Hayan
Sakr, Wael
Almardini, Nour
Urabi, Muaz
Dhar, Nivedita
Giorgadze, Tamar
Intravascular papillary endothelial hyperplasia of the bladder: Case report and review of the literature
title Intravascular papillary endothelial hyperplasia of the bladder: Case report and review of the literature
title_full Intravascular papillary endothelial hyperplasia of the bladder: Case report and review of the literature
title_fullStr Intravascular papillary endothelial hyperplasia of the bladder: Case report and review of the literature
title_full_unstemmed Intravascular papillary endothelial hyperplasia of the bladder: Case report and review of the literature
title_short Intravascular papillary endothelial hyperplasia of the bladder: Case report and review of the literature
title_sort intravascular papillary endothelial hyperplasia of the bladder: case report and review of the literature
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3507062/
https://www.ncbi.nlm.nih.gov/pubmed/23210010
http://dx.doi.org/10.4103/2231-0770.90917
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