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Hysterectomy in a male? A rare case report

INTRODUCTION: Persistent Mullerian duct syndrome is a rare form of male pseudo-hermaphroditism characterized by the presence of Mullerian duct structures in an otherwise phenotypically, as well as genotypically, normal man; only a few cases have been reported in the worldwide literature. A great var...

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Autores principales: Sherwani, Afak Yusuf, Shah, Abdul Qayoom, Wani, Abdul Majeed, Bashir, Ahmad Chalkoo, Bashir, Ahmad Khan, Sofi, Farooq Ahmad, Wani, Ashfaq Amin, Lone, Wasim, Sherwani, Ab Hamid, Sheikh, Mehmood Rashid, Sharma, Raj Reshi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4276263/
https://www.ncbi.nlm.nih.gov/pubmed/25481861
http://dx.doi.org/10.1016/j.ijscr.2014.10.020
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author Sherwani, Afak Yusuf
Shah, Abdul Qayoom
Wani, Abdul Majeed
Bashir, Ahmad Chalkoo
Bashir, Ahmad Khan
Sofi, Farooq Ahmad
Wani, Ashfaq Amin
Lone, Wasim
Sherwani, Ab Hamid
Sheikh, Mehmood Rashid
Sharma, Raj Reshi
author_facet Sherwani, Afak Yusuf
Shah, Abdul Qayoom
Wani, Abdul Majeed
Bashir, Ahmad Chalkoo
Bashir, Ahmad Khan
Sofi, Farooq Ahmad
Wani, Ashfaq Amin
Lone, Wasim
Sherwani, Ab Hamid
Sheikh, Mehmood Rashid
Sharma, Raj Reshi
author_sort Sherwani, Afak Yusuf
collection PubMed
description INTRODUCTION: Persistent Mullerian duct syndrome is a rare form of male pseudo-hermaphroditism characterized by the presence of Mullerian duct structures in an otherwise phenotypically, as well as genotypically, normal man; only a few cases have been reported in the worldwide literature. A great variety of organs have been found in indirect inguinal hernial sacs. PRESENTATION OF CASE: We report a case of 70 year old man, father of 4 children with unilateral cryptorchidism on the right side and left-sided obstructed inguinal hernia containing uterus and fallopian tube (that is, hernia uteri inguinalis; type I male form of persistent Mullerian duct syndrome) coincidentally detected during an operation for an obstructed left inguinal hernia. DISCUSSION: PMDS is usually coincidently detected during surgical operation, as was in our case. However pre-operative ultrasonography, computerized tomography and MRI allow possible pre-operative diagnosis.(3) CONCLUSION: In cases of unilateral or bilateral cryptorchidism associated with hernia, as in our patient's case, the possibility of PMDS should be kept in mind.
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spelling pubmed-42762632014-12-28 Hysterectomy in a male? A rare case report Sherwani, Afak Yusuf Shah, Abdul Qayoom Wani, Abdul Majeed Bashir, Ahmad Chalkoo Bashir, Ahmad Khan Sofi, Farooq Ahmad Wani, Ashfaq Amin Lone, Wasim Sherwani, Ab Hamid Sheikh, Mehmood Rashid Sharma, Raj Reshi Int J Surg Case Rep Article INTRODUCTION: Persistent Mullerian duct syndrome is a rare form of male pseudo-hermaphroditism characterized by the presence of Mullerian duct structures in an otherwise phenotypically, as well as genotypically, normal man; only a few cases have been reported in the worldwide literature. A great variety of organs have been found in indirect inguinal hernial sacs. PRESENTATION OF CASE: We report a case of 70 year old man, father of 4 children with unilateral cryptorchidism on the right side and left-sided obstructed inguinal hernia containing uterus and fallopian tube (that is, hernia uteri inguinalis; type I male form of persistent Mullerian duct syndrome) coincidentally detected during an operation for an obstructed left inguinal hernia. DISCUSSION: PMDS is usually coincidently detected during surgical operation, as was in our case. However pre-operative ultrasonography, computerized tomography and MRI allow possible pre-operative diagnosis.(3) CONCLUSION: In cases of unilateral or bilateral cryptorchidism associated with hernia, as in our patient's case, the possibility of PMDS should be kept in mind. Elsevier 2014-10-30 /pmc/articles/PMC4276263/ /pubmed/25481861 http://dx.doi.org/10.1016/j.ijscr.2014.10.020 Text en © 2014 Surgical Associates Ltd. Published by Elsevier Ltd. All rights reserved. http://creativecommons.org/licenses/by-nc-nd/3.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/3.0/).
spellingShingle Article
Sherwani, Afak Yusuf
Shah, Abdul Qayoom
Wani, Abdul Majeed
Bashir, Ahmad Chalkoo
Bashir, Ahmad Khan
Sofi, Farooq Ahmad
Wani, Ashfaq Amin
Lone, Wasim
Sherwani, Ab Hamid
Sheikh, Mehmood Rashid
Sharma, Raj Reshi
Hysterectomy in a male? A rare case report
title Hysterectomy in a male? A rare case report
title_full Hysterectomy in a male? A rare case report
title_fullStr Hysterectomy in a male? A rare case report
title_full_unstemmed Hysterectomy in a male? A rare case report
title_short Hysterectomy in a male? A rare case report
title_sort hysterectomy in a male? a rare case report
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4276263/
https://www.ncbi.nlm.nih.gov/pubmed/25481861
http://dx.doi.org/10.1016/j.ijscr.2014.10.020
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