先天性单侧阴囊发育不全：一种罕见实体的报告。
Congenital hemiscrotal agenesis: report of a rare entity.
机构信息
Bakirköy Dr. Sadi Konuk Training and Research Hospital, Department of Pediatric Surgery, İstanbul, Turkey.
出版信息
J Pediatr Urol. 2013 Feb;9(1):e76-7. doi: 10.1016/j.jpurol.2012.09.005. Epub 2012 Oct 6.
PMID:23044375
Abstract
Congenital scrotal agenesis is the rarest anomaly of scrotal development disorder and is characterized by the absence of scrotal rugae in the perineum between the penis and anus. We report here a case of hemiscrotal agenesis in a 2-year-old boy. To the best of our knowledge, our patient is the second reported case of hemiscrotal agenesis in the English literature.
摘要
先天性阴囊发育不全是阴囊发育障碍中最罕见的异常，其特征是阴茎和肛门之间的会阴部没有阴囊皱襞。我们在此报告一例 2 岁男孩的单侧阴囊发育不全病例。据我们所知，我们的患者是英文文献中第二例报道的单侧阴囊发育不全病例。
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