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合并肛门直肠畸形的梅干腹综合征

Prune-belly syndrome with anorectal malformation.

作者信息

Mahajan J K, Ojha S, Rao K L N

机构信息

Department of Pediatric Surgery, Advanced Pediatric Center, Postgraduate Institute of Medical Education and Research, Chandigarh, India.

出版信息

Eur J Pediatr Surg. 2004 Oct;14(5):351-4. doi: 10.1055/s-2004-817961.

Abstract

Associated abnormalities of other organ systems result in considerable long-term morbidity in patients of prune-belly syndrome (PBS). The gastrointestinal anomalies commonly observed with PBS are persistence of the embryonic wide mesentery and absence of fixation to the posterior abdominal wall, whereas anorectal malformations (ARM) are rarely associated with PBS. We describe one such case of PBS associated with high ARM and urethral stenosis in a one-day-old male newborn. The neonate underwent preliminary sigmoid colostomy for ARM, but he subsequently developed necrotizing gastritis and gastric perforation in the postoperative period and had to undergo partial gastrectomy and vesicostomy. The neonate developed fatal septicemia after second surgery. A review of all the reported cases of this association is presented and the dilemmas in the management of these cases are discussed.

摘要

其他器官系统的相关异常会导致梨状腹综合征(PBS)患者出现相当严重的长期发病率。PBS常见的胃肠道异常是胚胎期宽肠系膜持续存在且未固定于后腹壁,而肛门直肠畸形(ARM)很少与PBS相关。我们描述了一例1日龄男婴患有PBS并伴有高位ARM和尿道狭窄的病例。该新生儿因ARM接受了初步的乙状结肠造口术,但术后出现坏死性胃炎和胃穿孔,不得不接受部分胃切除术和膀胱造瘘术。该新生儿在第二次手术后发生致命性败血症。本文对所有已报道的这种关联病例进行了综述,并讨论了这些病例管理中的困境。

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