Cargando…

Persistent Mullerian duct syndrome with testicular seminoma: A report of two cases

Persistent Mullerian duct syndrome is a rare form of male pseudohermaphroditism, characterized by the presence of the Mullerian duct structures in an otherwise phenotypically as well as genotypically normal male. We report two cases of males with cryptorchidism, and seminoma in the undescended abdom...

Descripción completa

Detalles Bibliográficos
Autores principales: Inuganti, Renuka V., Bala, G. Salia, Kumar, Y. Kiran, Bharathi, Y. Krishna
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Medknow Publications 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3193747/
https://www.ncbi.nlm.nih.gov/pubmed/22022070
http://dx.doi.org/10.4103/0970-1591.85451
_version_ 1782213877546614784
author Inuganti, Renuka V.
Bala, G. Salia
Kumar, Y. Kiran
Bharathi, Y. Krishna
author_facet Inuganti, Renuka V.
Bala, G. Salia
Kumar, Y. Kiran
Bharathi, Y. Krishna
author_sort Inuganti, Renuka V.
collection PubMed
description Persistent Mullerian duct syndrome is a rare form of male pseudohermaphroditism, characterized by the presence of the Mullerian duct structures in an otherwise phenotypically as well as genotypically normal male. We report two cases of males with cryptorchidism, and seminoma in the undescended abdominal testis along with Mullerian duct derivatives (uterus and fallopian tube).
format Online
Article
Text
id pubmed-3193747
institution National Center for Biotechnology Information
language English
publishDate 2011
publisher Medknow Publications
record_format MEDLINE/PubMed
spelling pubmed-31937472011-10-21 Persistent Mullerian duct syndrome with testicular seminoma: A report of two cases Inuganti, Renuka V. Bala, G. Salia Kumar, Y. Kiran Bharathi, Y. Krishna Indian J Urol Case Report Persistent Mullerian duct syndrome is a rare form of male pseudohermaphroditism, characterized by the presence of the Mullerian duct structures in an otherwise phenotypically as well as genotypically normal male. We report two cases of males with cryptorchidism, and seminoma in the undescended abdominal testis along with Mullerian duct derivatives (uterus and fallopian tube). Medknow Publications 2011 /pmc/articles/PMC3193747/ /pubmed/22022070 http://dx.doi.org/10.4103/0970-1591.85451 Text en Copyright: © Indian Journal of Urology http://creativecommons.org/licenses/by-nc-sa/3.0 This is an open-access article distributed under the terms of the Creative Commons Attribution-Noncommercial-Share Alike 3.0 Unported, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Case Report
Inuganti, Renuka V.
Bala, G. Salia
Kumar, Y. Kiran
Bharathi, Y. Krishna
Persistent Mullerian duct syndrome with testicular seminoma: A report of two cases
title Persistent Mullerian duct syndrome with testicular seminoma: A report of two cases
title_full Persistent Mullerian duct syndrome with testicular seminoma: A report of two cases
title_fullStr Persistent Mullerian duct syndrome with testicular seminoma: A report of two cases
title_full_unstemmed Persistent Mullerian duct syndrome with testicular seminoma: A report of two cases
title_short Persistent Mullerian duct syndrome with testicular seminoma: A report of two cases
title_sort persistent mullerian duct syndrome with testicular seminoma: a report of two cases
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3193747/
https://www.ncbi.nlm.nih.gov/pubmed/22022070
http://dx.doi.org/10.4103/0970-1591.85451
work_keys_str_mv AT inugantirenukav persistentmullerianductsyndromewithtesticularseminomaareportoftwocases
AT balagsalia persistentmullerianductsyndromewithtesticularseminomaareportoftwocases
AT kumarykiran persistentmullerianductsyndromewithtesticularseminomaareportoftwocases
AT bharathiykrishna persistentmullerianductsyndromewithtesticularseminomaareportoftwocases