| Literature DB >> 28584567 |
Khalid N Alharbi1, Ayman O Khushaim2, Mohannad Alrasheed2, Mohammed Akhtar3, Mohammed Neimatallah2.
Abstract
This case involved a 36-year-old adult male who presented with an unusual inguinal hernia in which the uterus and fallopian tubes were identified as contents of the inguinal hernia sac. These findings reflected a rare autosomal recessive developmental syndrome known as PMDS (persistent Müllerian duct syndrome). The diagnosis was established and confirmed via radiological-mainly MRI-investigation.Entities:
Keywords: Abdominal CT; Abdominal MRI; Hernia uteri inguinalis; Müllerian duct; PMDS; Persistent Müllerian duct syndrome; Scrotal ultrasound; Wolffian duct
Mesh:
Year: 2017 PMID: 28584567 PMCID: PMC5441465 DOI: 10.3941/jrcr.v11i3.3027
Source DB: PubMed Journal: J Radiol Case Rep ISSN: 1943-0922