伴有多种异常的完全性阴茎重复畸形的手术治疗
Surgical management of complete penile duplication accompanied by multiple anomalies.
作者信息
Karaca Irfan, Turk Erdal, Ucan A Basak, Yayla Derya, Itirli Gulcin, Ercal Derya
机构信息
Department of Pediatric Surgery, Faculty of Medicine, Izmir University, Izmir, Turkey;
Departments of Pediatric Surgery, Dr. Behcet Uz Children's Hospital, Izmir/Turkey;
出版信息
Can Urol Assoc J. 2014 Sep;8(9-10):E741-3. doi: 10.5489/cuaj.2049.
Diphallus (penile duplication) is very rare and seen once every 5.5 million births. It can be isolated, but is usually accompanied by other congenital anomalies. Previous studies have reported many concurrent anomalies, such as bladder extrophy, cloacal extrophy, duplicated bladder, scrotal abnormalities, hypospadias, separated symphysis pubis, intestinal anomalies and imperforate anus; no penile duplication case accompanied by omphalocele has been reported. We present the surgical management of a patient with multiple anomalies, including complete penile duplication, hypo-gastric omphalocele and extrophic rectal duplication.
双阴茎（阴茎重复畸形）极为罕见，每550万例出生中才会出现1例。它可以单独存在，但通常伴有其他先天性异常。既往研究报告了许多并发异常，如膀胱外翻、泄殖腔外翻、重复膀胱、阴囊异常、尿道下裂、耻骨联合分离、肠道异常和肛门闭锁；尚未有双阴茎病例合并脐膨出的报道。我们介绍了1例患有多种异常的患者的手术治疗情况，这些异常包括完全性双阴茎、下腹脐膨出和直肠重复畸形伴外翻。
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