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Mullerianosis of the Urinary Bladder: A Case Report

Mullerianosis is a rare entity consisting of an admixture of 2 or more of the following tissues: endometriosis, endocervicosis, and endosalpingiosis. It most commonly affects the urinary bladder and affects females of fertile age. It presents clinically as hematuria, dysuria, and pelvic pain which m...

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Autores principales: Amir, Rawan Abdul Razack, Taheini, Khalid M., Sheikh, Salwa S.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: S. Karger AG 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5903129/
https://www.ncbi.nlm.nih.gov/pubmed/29681822
http://dx.doi.org/10.1159/000487429
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author Amir, Rawan Abdul Razack
Taheini, Khalid M.
Sheikh, Salwa S.
author_facet Amir, Rawan Abdul Razack
Taheini, Khalid M.
Sheikh, Salwa S.
author_sort Amir, Rawan Abdul Razack
collection PubMed
description Mullerianosis is a rare entity consisting of an admixture of 2 or more of the following tissues: endometriosis, endocervicosis, and endosalpingiosis. It most commonly affects the urinary bladder and affects females of fertile age. It presents clinically as hematuria, dysuria, and pelvic pain which may be associated with menstruation. Radiologically and macroscopically, it typically presents as a polypoid mass in the dome or posterior wall of the bladder. Histologically, it consists of glands of varying size lined by endometrial, endocervical, or tubal epithelium. Mullerianosis clinically and histologically mimics other benign and malignant lesions. Herein we report a case of mullerianosis of the urinary bladder. This is a rare lesion with less than 20 cases reported in the literature thus far. We believe raising awareness of this poorly recognized entity is of utmost significance in order to avoid misdiagnosis and the following unnecessary radical procedures.
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spelling pubmed-59031292018-04-20 Mullerianosis of the Urinary Bladder: A Case Report Amir, Rawan Abdul Razack Taheini, Khalid M. Sheikh, Salwa S. Case Rep Oncol Case Report Mullerianosis is a rare entity consisting of an admixture of 2 or more of the following tissues: endometriosis, endocervicosis, and endosalpingiosis. It most commonly affects the urinary bladder and affects females of fertile age. It presents clinically as hematuria, dysuria, and pelvic pain which may be associated with menstruation. Radiologically and macroscopically, it typically presents as a polypoid mass in the dome or posterior wall of the bladder. Histologically, it consists of glands of varying size lined by endometrial, endocervical, or tubal epithelium. Mullerianosis clinically and histologically mimics other benign and malignant lesions. Herein we report a case of mullerianosis of the urinary bladder. This is a rare lesion with less than 20 cases reported in the literature thus far. We believe raising awareness of this poorly recognized entity is of utmost significance in order to avoid misdiagnosis and the following unnecessary radical procedures. S. Karger AG 2018-03-27 /pmc/articles/PMC5903129/ /pubmed/29681822 http://dx.doi.org/10.1159/000487429 Text en Copyright © 2018 by S. Karger AG, Basel http://creativecommons.org/licenses/by-nc/4.0/ This article is licensed under the Creative Commons Attribution-NonCommercial-4.0 International License (CC BY-NC) (http://www.karger.com/Services/OpenAccessLicense). Usage and distribution for commercial purposes requires written permission.
spellingShingle Case Report
Amir, Rawan Abdul Razack
Taheini, Khalid M.
Sheikh, Salwa S.
Mullerianosis of the Urinary Bladder: A Case Report
title Mullerianosis of the Urinary Bladder: A Case Report
title_full Mullerianosis of the Urinary Bladder: A Case Report
title_fullStr Mullerianosis of the Urinary Bladder: A Case Report
title_full_unstemmed Mullerianosis of the Urinary Bladder: A Case Report
title_short Mullerianosis of the Urinary Bladder: A Case Report
title_sort mullerianosis of the urinary bladder: a case report
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5903129/
https://www.ncbi.nlm.nih.gov/pubmed/29681822
http://dx.doi.org/10.1159/000487429
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