Abstract
Context:Persistent Mullerian duct syndrome (PMDS) is a rare disorder. It is a type of male pseudohermaphroditism, usually presenting as “Hernia Uteri Inguinalis”.Aims:This study aims to present our experience of PMDS, over a 7-year period.Settings and Design:Our center is a tertiary care facility, situated in Tamil Nadu, a southern state of India.Subjects and Methods:This is a retrospective study. The study period was from 2007 to 2015. Seven cases presented during that period. The difficulties in diagnosis, treatment options discussed, along with a review of literature are presented.Results:Seven cases of PMDS presented over 8 years. Only four were diagnosed preoperatively. Mullerian remnants were excised in five cases.Conclusions:PMDS is rare. Orchiopexy should be the goal of treatment.
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