Journal of Clinical and Diagnostic Research, ISSN - 0973 - 709X

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Case report
Table of Contents - Year : 2017 | Month : August | Volume : 11 | Issue : 8 | Page : PD19 - PD20

Hemiscrotal Agenesis: A Rare Congenital Anomaly PD19-PD20

Alexandros Psarris, Anastasia Dimopoulou, Emmanouil Iakomidis, Nikolaos Zavras, Georgios Vaos

Correspondence
Dr. Anastasia Dimopoulou,
Consultant, Department of Paediatric Surgery, Attikon University General Hospital, Rimini Street 1, 124 62, Athens, Greece.
Email: natasa_dimo@hotmail.com

Hemiscrotal Agenesis (HSA) is the rarest developmental malformation of the scrotum. It is characterized by the absence of either half of the scrotal rugae with an intact midline raphe. We report the case of a 16-month-old boy with HSA, with an island of scrotal tissue in the pubic tubercle region and ipsilateral cryptorchidism. To our knowledge, this is the first case of HSA with heterotopic development of scrotal tissue.