| Literature DB >> 32775671 |
Alexandra Pearce1, Chad Crigger1, Ali Hajiran1, Osama Al-Omar1.
Abstract
Background: Persistent Mullerian duct syndrome (PMDS) is a rare disorder of sexual development that results in the presence of internal female reproductive structures in male children who are otherwise phenotypically normal. The removal of the Mullerian structures is suggested, as they pose a risk for future malignancy. Case Presentation: In this study, we present the case of a 14-month-old male infant who initially presented with bilateral nonpalpable undescended testes and was later diagnosed with PMDS. The effective removal of the Mullerian structures and bilateral orchiopexy was performed using robot-assisted laparoscopy, a novel approach for such a scenario.Entities:
Keywords: disorder of sexual development; pediatrics; persistent Mullerian duct syndrome; robot-assisted
Year: 2020 PMID: 32775671 PMCID: PMC7383418 DOI: 10.1089/cren.2019.0079
Source DB: PubMed Journal: J Endourol Case Rep ISSN: 2379-9889