Hemiscrotal Agenesis: A Rare Congenital Anomaly
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...
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doaj-c8446a45e5be4b9d9c3f741fab80f39a2020-11-25T03:17:32ZengJCDR Research and Publications Private LimitedJournal of Clinical and Diagnostic Research2249-782X0973-709X2017-08-01118PD19PD2010.7860/JCDR/2017/28605.10507Hemiscrotal Agenesis: A Rare Congenital AnomalyAlexandros Psarris0Anastasia Dimopoulou1Emmanouil Iakomidis2Nikolaos Zavras3Georgios Vaos4Resident, Department of Gynaecology, Agios Savvas Cancer Hospital, Athens, Greece.Consultant, Department of Paediatric Surgery, Attikon University General Hospital, School of Medicine, National and Kapodistrian University of Athens, Athens, Greece.Senior Resident, Department of Paediatric Surgery, Agia Sofia Children’s Hospital, Athens, Greece.Assistant Professor, Department of Paediatric Surgery, Attikon University General Hospital, School of Medicine, National and Kapodistrian University of Athens, Athens, Greece. Professor, Department of Paediatric Surgery, Attikon University General Hospital, School of Medicine, National and Kapodistrian University of Athens, Athens, Greece.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. https://jcdr.net/articles/PDF/10507/28605_270617_28605_CE[Ra1]_F[RU]_PF1_(MJ_PY)_PFA(MJ_GG)_(SY_MJ_GG).pdfcryptorchidismperineumscrotum |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Alexandros Psarris Anastasia Dimopoulou Emmanouil Iakomidis Nikolaos Zavras Georgios Vaos |
spellingShingle |
Alexandros Psarris Anastasia Dimopoulou Emmanouil Iakomidis Nikolaos Zavras Georgios Vaos Hemiscrotal Agenesis: A Rare Congenital Anomaly Journal of Clinical and Diagnostic Research cryptorchidism perineum scrotum |
author_facet |
Alexandros Psarris Anastasia Dimopoulou Emmanouil Iakomidis Nikolaos Zavras Georgios Vaos |
author_sort |
Alexandros Psarris |
title |
Hemiscrotal Agenesis: A Rare Congenital Anomaly |
title_short |
Hemiscrotal Agenesis: A Rare Congenital Anomaly |
title_full |
Hemiscrotal Agenesis: A Rare Congenital Anomaly |
title_fullStr |
Hemiscrotal Agenesis: A Rare Congenital Anomaly |
title_full_unstemmed |
Hemiscrotal Agenesis: A Rare Congenital Anomaly |
title_sort |
hemiscrotal agenesis: a rare congenital anomaly |
publisher |
JCDR Research and Publications Private Limited |
series |
Journal of Clinical and Diagnostic Research |
issn |
2249-782X 0973-709X |
publishDate |
2017-08-01 |
description |
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. |
topic |
cryptorchidism perineum scrotum |
url |
https://jcdr.net/articles/PDF/10507/28605_270617_28605_CE[Ra1]_F[RU]_PF1_(MJ_PY)_PFA(MJ_GG)_(SY_MJ_GG).pdf |
work_keys_str_mv |
AT alexandrospsarris hemiscrotalagenesisararecongenitalanomaly AT anastasiadimopoulou hemiscrotalagenesisararecongenitalanomaly AT emmanouiliakomidis hemiscrotalagenesisararecongenitalanomaly AT nikolaoszavras hemiscrotalagenesisararecongenitalanomaly AT georgiosvaos hemiscrotalagenesisararecongenitalanomaly |
_version_ |
1724631636845264896 |