首页> 美国卫生研究院文献>World Journal of Gastroenterology >Idiopathic abdominal cocoon syndrome with unilateral abdominal cryptorchidism and greater omentum hypoplasia in a young case of small bowel obstruction
【2h】

Idiopathic abdominal cocoon syndrome with unilateral abdominal cryptorchidism and greater omentum hypoplasia in a young case of small bowel obstruction

机译:年轻的小肠梗阻病例特发性腹茧综合症伴单侧腹部隐睾和大网膜发育不全

代理获取
本网站仅为用户提供外文OA文献查询和代理获取服务,本网站没有原文。下单后我们将采用程序或人工为您竭诚获取高质量的原文,但由于OA文献来源多样且变更频繁,仍可能出现获取不到、文献不完整或与标题不符等情况,如果获取不到我们将提供退款服务。请知悉。

摘要

Abdominal cocoon syndrome (ACS) is a rare cause of intestinal obstruction due to total or partial encapsulation of the small intestine by a fibrocollagenous membrane. Idiopathic ACS with abdominal cryptorchidism and greater omentum hypoplasia is even rarer clinically. We successfully treated a 26-year-old male case of small bowel obstruction with acute peritonitis. He was finally diagnosed with idiopathic ACS with unilateral abdominal cryptorchidism and greater omentum hypoplasia during exploratory laparotomy. He then underwent enterolysis, cryptorchidectomy, and appendectomy. He recovered gradually from the operations and early postoperative inflammatory ileus. There has been no recurrence of intestinal obstruction since the operation, and he is still in follow-up. We analyzed his clinical data and retrospectively reviewed the literature, and our findings may be helpful for the clinical diagnosis and treatment on ACS.
机译:腹部茧综合症(ACS)是由于纤维胶原膜完全或部分包封小肠而引起肠梗阻的罕见原因。具有腹部隐睾症和大网膜发育不全的特发性ACS在临床上更为罕见。我们成功地治疗了26岁的男性小肠梗阻伴急性腹膜炎。最终他在探索性剖腹手术中被诊断为特发性ACS,伴有单侧腹部隐睾和大网膜发育不全。然后,他接受了小肠溶解,隐睾切除术和阑尾切除术。他从手术和术后早期炎症性肠梗阻逐渐恢复。自手术以来没有再发生肠梗阻,他仍在随访中。我们分析了他的临床资料并回顾性地回顾了文献,我们的发现可能有助于ACS的临床诊断和治疗。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
代理获取

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号