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Persistent Mullerian duct syndrome (PMDS): Case report and review of literature
Persistent Mullerian duct syndrome (PMDS) is a rare form of male pseudohermaphroditism (MPH) which characterized by the presence of uterus, fallopian tubes and upper part of vagina in an otherwise normally differentiated 46, XY male. The syndrome is caused by either an insufficient amount of antimül...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9073291/ https://www.ncbi.nlm.nih.gov/pubmed/35530558 http://dx.doi.org/10.1016/j.eucr.2022.102031 |
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author | Alanazi, Abdullah B. Aldhowayan, Afrah Almuhanna, Mousa M. Alghamdi, Abdullah M. |
author_facet | Alanazi, Abdullah B. Aldhowayan, Afrah Almuhanna, Mousa M. Alghamdi, Abdullah M. |
author_sort | Alanazi, Abdullah B. |
collection | PubMed |
description | Persistent Mullerian duct syndrome (PMDS) is a rare form of male pseudohermaphroditism (MPH) which characterized by the presence of uterus, fallopian tubes and upper part of vagina in an otherwise normally differentiated 46, XY male. The syndrome is caused by either an insufficient amount of antimüllerian hormone AMH or by insensitivity of the target organ to this factor, It is usually discovered in patient who assessed for infertility, cryptorchidism or during intra-abdominal surgery. Herein We report a rare presentation case of PMDS with intra-abdominal mass which came to be seminoma. |
format | Online Article Text |
id | pubmed-9073291 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
spelling | pubmed-90732912022-05-07 Persistent Mullerian duct syndrome (PMDS): Case report and review of literature Alanazi, Abdullah B. Aldhowayan, Afrah Almuhanna, Mousa M. Alghamdi, Abdullah M. Urol Case Rep Oncology Persistent Mullerian duct syndrome (PMDS) is a rare form of male pseudohermaphroditism (MPH) which characterized by the presence of uterus, fallopian tubes and upper part of vagina in an otherwise normally differentiated 46, XY male. The syndrome is caused by either an insufficient amount of antimüllerian hormone AMH or by insensitivity of the target organ to this factor, It is usually discovered in patient who assessed for infertility, cryptorchidism or during intra-abdominal surgery. Herein We report a rare presentation case of PMDS with intra-abdominal mass which came to be seminoma. Elsevier 2022-02-21 /pmc/articles/PMC9073291/ /pubmed/35530558 http://dx.doi.org/10.1016/j.eucr.2022.102031 Text en © 2022 Published by Elsevier Inc. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/). |
spellingShingle | Oncology Alanazi, Abdullah B. Aldhowayan, Afrah Almuhanna, Mousa M. Alghamdi, Abdullah M. Persistent Mullerian duct syndrome (PMDS): Case report and review of literature |
title | Persistent Mullerian duct syndrome (PMDS): Case report and review of literature |
title_full | Persistent Mullerian duct syndrome (PMDS): Case report and review of literature |
title_fullStr | Persistent Mullerian duct syndrome (PMDS): Case report and review of literature |
title_full_unstemmed | Persistent Mullerian duct syndrome (PMDS): Case report and review of literature |
title_short | Persistent Mullerian duct syndrome (PMDS): Case report and review of literature |
title_sort | persistent mullerian duct syndrome (pmds): case report and review of literature |
topic | Oncology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9073291/ https://www.ncbi.nlm.nih.gov/pubmed/35530558 http://dx.doi.org/10.1016/j.eucr.2022.102031 |
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