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长发公主综合征。一例报告及文献综述。

The Rapunzel syndrome. Report of a case and review of the literature.

作者信息

Duncan N D, Aitken R, Venugopal S, West W, Carpenter R

机构信息

Department of Surgery, U.W.I., Jamaica.

出版信息

West Indian Med J. 1994 Jun;43(2):63-5.

PMID:7941500
Abstract

The Rapunzel Syndrome, a rare manifestation of trichobezoar, occurs when bolus gastrointestinal obstruction is produced by an unusual trichobezoar with a long tail that extends to or beyond the ileocaecal valve. A five-year-old Jamaican girl presented with this abnormality and was found at laparotomy also to have an ileo-ileal intussusception. For the Rapunzel Syndrome, we recommend bezoar extraction at laparotomy via multiple enterotomies. In addition, psychiatric evaluation and therapy is essential due to the commonly associated finding of underlying emotional stress.

摘要

长发公主综合征是毛粪石的一种罕见表现,当一种不寻常的、带有长尾巴且延伸至回盲瓣或超过回盲瓣的毛粪石导致胃肠道团块梗阻时就会发生。一名5岁的牙买加女孩出现了这种异常情况,剖腹探查时还发现有回肠-回肠套叠。对于长发公主综合征,我们建议通过多处肠切开术在剖腹手术时取出粪石。此外,由于通常会发现潜在的情绪压力,进行精神评估和治疗至关重要。

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