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先天性巨包皮的手术矫正

Surgical correction of congenital megaprepuce.

作者信息

Shenoy M U, Rance C H

机构信息

Department of Paediatric Surgery, Nottingham City Hospital, UK.

出版信息

Pediatr Surg Int. 1999;15(8):593-4. doi: 10.1007/s003830050683.

Abstract

Congenital megaprepuce (CMP) is a rare entity. Two infant boys presented with a tight congenital phimosis resulting in an excessively baggy, urine-filled prepuce and a swollen scrotum. Compression of the scrotum resulted in drainage of urine. We feel this to be a separate entity from a buried penis and recommend early surgery. The phimotic tip of the foreskin was excised and the inner layer preserved to cover the full length of the penile shaft. The outer layer of the foreskin, in reality the penoscrotal junction, was anchored to the base of the penile shaft. A V-shaped edge of ventral skin was excised and the edges approximated, giving the appearance of median raphe. The final appearance was that of a circumcised penis. A third patient awaits operation.

摘要

先天性巨包皮(CMP)是一种罕见病症。两名男婴表现为先天性包茎过紧,导致包皮过度松弛、充满尿液,阴囊肿胀。压迫阴囊会有尿液排出。我们认为这是一种有别于隐匿阴茎的独立病症,并建议早期手术。切除包皮的狭窄尖端,保留内层以覆盖阴茎体全长。包皮外层,实际上是阴茎阴囊交界处,固定于阴茎体基部。切除腹侧皮肤的V形边缘,使边缘对合,形成正中缝外观。最终外观类似包皮环切术后的阴茎。第三名患者等待手术。

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