Author:
Zhou Hui,Xu Jinling,Xie Xingwang,Han Jiantao
Abstract
Abstract
Background
Cocoon abdomen is a relatively rare abdominal disease characterized by the total or partial encasement of the small intestinal by a dense fibro-collagenous membrane.
Case presentation
We reported an unusual case of idiopathic cocoon abdomen with congenital colon malrotation. Laparotomy and sac release were performed on the patient. The patient was no recurrence 6 months after operation. A literature review was also performed.
Conclusion
Preoperative diagnosis of abdominal cocoon is difficult. A careful history, physical examination and appropriate radiology may be helpful in making a definitive diagnosis. If conservative treatment can’t relieve symptoms effectively, surgery is currently considered to be important in the management of this disease.
Publisher
Springer Science and Business Media LLC
Reference22 articles.
1. Foo KT, Ng KC, Rauff A, Foong WC, Sinniah R. Unusual small intestinal obstruction in adolescent girls: the abdominal cocoon. Br J Surg. 1978;65:427–30.
2. Kumar R, Singh PK. Masiullah. Primary sclerosing encapsulating peritonitis presenting as recurrent intestinal obstruction. Clin Gastroenterol Hepatol. 2017;15:e84–5.
3. Cleffken B, Sie G, Riedl R, Heineman E. Idiopathic sclerosing encapsulating peritonitis in a young female-diagnosis of abdominal cocoon. J Pediatr Surg. 2008;43:e27–30.
4. Tu JF, Huang XF, Zhu GB, Liao Y, Jiang FZ. Comprehensive analysis of 203 cases of abdominal cramps. Chin J Gastrointest Surg. 2006;9:133–5.
5. Yi L, Ning L, Zhu WM, et al. Clinical analysis of 67 cases of primary abdominal cramps surgery. Chin J Surg. 2013;51:139–41.
Cited by
4 articles.
订阅此论文施引文献
订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献