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针对腹部肌肉缺损(“梅干腹”)综合征患者的全手术重建。

Total surgical reconstruction for patients with abdominal muscular deficiency ("prune-belly") syndrome.

作者信息

Randolph J G

出版信息

J Pediatr Surg. 1977 Dec;12(6):1033-43. doi: 10.1016/0022-3468(77)90616-9.

Abstract

In the past decade, seven children with the prune-belly syndrome have been seen. Their management has consisted of immediate high tubeless urinary diversion, usually pyelostomy. Thereafter, total reconstruction has been carried out, preferably at one stage. This consists of (1) bilateral shortening, tapering and reimplantation of the ureters, (2) reduction cystoplasty, (3) bilateral orchiopexy, and (4) excision of that part of the abdominal wall that is most redundant and least endowed with musculature. This early effort at mechanical reconstruction has led to gratifying progress in six of the seven children.

摘要

在过去十年中,我们诊治了7例患有梅干腹综合征的患儿。对他们的治疗包括立即进行高位无管尿液转流术,通常是肾盂造瘘术。此后,进行了全面的重建手术,最好是一期完成。这包括:(1)双侧输尿管缩短、变细并重新植入;(2)膀胱缩小成形术;(3)双侧睾丸固定术;(4)切除腹壁最松弛且肌肉最少的部分。这种早期的机械重建努力已使7例患儿中的6例取得了令人满意的进展。

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