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Parameatal Median Raphe Cyst: A Case Report of a Midline Developmental Defect of True Urogenital Origin

Median raphe cyst (MRC) is an uncommon, asymptomatic benign lesion, that may present anywhere on the midline ridge between the external urethral meatus and the anus. Although they are developmental in origin, they often present in the postpubertal age, aggravated by trauma, and are frequently infect...

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Autores principales: Sharma, Aseem, Agrawal, Sandip, Vishwanath, Tejas, Ghate, Smita, Dhurat, Rachita, Chahal, Kiran
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Wolters Kluwer - Medknow 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7247623/
https://www.ncbi.nlm.nih.gov/pubmed/32477982
http://dx.doi.org/10.4103/idoj.IDOJ_122_19
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author Sharma, Aseem
Agrawal, Sandip
Vishwanath, Tejas
Ghate, Smita
Dhurat, Rachita
Chahal, Kiran
author_facet Sharma, Aseem
Agrawal, Sandip
Vishwanath, Tejas
Ghate, Smita
Dhurat, Rachita
Chahal, Kiran
author_sort Sharma, Aseem
collection PubMed
description Median raphe cyst (MRC) is an uncommon, asymptomatic benign lesion, that may present anywhere on the midline ridge between the external urethral meatus and the anus. Although they are developmental in origin, they often present in the postpubertal age, aggravated by trauma, and are frequently infected secondarily. MRCs are often misdiagnosed as epidermal cysts, steatocystoma multiplex, and eccrine cystadenomas. They are underrecognized and less than ten case reports exist from the Indian subcontinent. We, herein report a male with an immunohistochemically proven parameatal MRC.
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spelling pubmed-72476232020-05-29 Parameatal Median Raphe Cyst: A Case Report of a Midline Developmental Defect of True Urogenital Origin Sharma, Aseem Agrawal, Sandip Vishwanath, Tejas Ghate, Smita Dhurat, Rachita Chahal, Kiran Indian Dermatol Online J Case Report Median raphe cyst (MRC) is an uncommon, asymptomatic benign lesion, that may present anywhere on the midline ridge between the external urethral meatus and the anus. Although they are developmental in origin, they often present in the postpubertal age, aggravated by trauma, and are frequently infected secondarily. MRCs are often misdiagnosed as epidermal cysts, steatocystoma multiplex, and eccrine cystadenomas. They are underrecognized and less than ten case reports exist from the Indian subcontinent. We, herein report a male with an immunohistochemically proven parameatal MRC. Wolters Kluwer - Medknow 2020-03-09 /pmc/articles/PMC7247623/ /pubmed/32477982 http://dx.doi.org/10.4103/idoj.IDOJ_122_19 Text en Copyright: © 2020 Indian Dermatology Online Journal http://creativecommons.org/licenses/by-nc-sa/4.0 This is an open access journal, and articles are distributed under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike 4.0 License, which allows others to remix, tweak, and build upon the work non-commercially, as long as appropriate credit is given and the new creations are licensed under the identical terms.
spellingShingle Case Report
Sharma, Aseem
Agrawal, Sandip
Vishwanath, Tejas
Ghate, Smita
Dhurat, Rachita
Chahal, Kiran
Parameatal Median Raphe Cyst: A Case Report of a Midline Developmental Defect of True Urogenital Origin
title Parameatal Median Raphe Cyst: A Case Report of a Midline Developmental Defect of True Urogenital Origin
title_full Parameatal Median Raphe Cyst: A Case Report of a Midline Developmental Defect of True Urogenital Origin
title_fullStr Parameatal Median Raphe Cyst: A Case Report of a Midline Developmental Defect of True Urogenital Origin
title_full_unstemmed Parameatal Median Raphe Cyst: A Case Report of a Midline Developmental Defect of True Urogenital Origin
title_short Parameatal Median Raphe Cyst: A Case Report of a Midline Developmental Defect of True Urogenital Origin
title_sort parameatal median raphe cyst: a case report of a midline developmental defect of true urogenital origin
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7247623/
https://www.ncbi.nlm.nih.gov/pubmed/32477982
http://dx.doi.org/10.4103/idoj.IDOJ_122_19
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