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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...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Elsevier
2014
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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. |
format | Online Article Text |
id | pubmed-4276263 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
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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