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长发公主综合征:一例罕见毛粪石病例的全面综述

Rapunzel syndrome: a comprehensive review of an unusual case of trichobezoar.

作者信息

Gonuguntla Veena, Joshi Divya-Devi

机构信息

Department of Pediatrics, Marshfield Clinic, 1000 North Oak Avenue, Marshfield, WI 54449, USA.

出版信息

Clin Med Res. 2009 Sep;7(3):99-102. doi: 10.3121/cmr.2009.822. Epub 2009 Jul 22.

Abstract

An unusual form of bezoar extending from the stomach to the small intestine or beyond has been described as Rapunzel syndrome. Bezoars are concretions in the gastrointestinal tract that increase in size by continuous accumulation of non-absorbable food or fibers. Most bezoars in children are trichobezoars from swallowed hair from the head, dolls, or brushes. Trichobezoars typically cause abdominal pain and nausea, but can also present as an asymptomatic abdominal mass, progressing to abdominal obstruction and perforation. Trichobezoar with Rapunzel syndrome is an uncommon diagnosis in children with less than 40 cases reported. It is predominantly found in emotionally disturbed or mentally retarded youngsters. We present the youngest case of Rapunzel syndrome in the United States, a 5-year-old girl with mental retardation who presented with abdominal pain, vomiting and a non-tender abdominal mass.

摘要

一种从胃延伸至小肠或更远部位的特殊类型的胃石被称为长发公主综合征。胃石是胃肠道内的凝结物,通过不可吸收的食物或纤维的持续积累而增大。儿童中的大多数胃石是毛胃石,由吞食头部毛发、玩偶毛发或刷子毛发所致。毛胃石通常会引起腹痛和恶心,但也可能表现为无症状的腹部肿块,进而发展为肠梗阻和穿孔。伴有长发公主综合征的毛胃石在儿童中是一种罕见的诊断,报告病例少于40例。它主要见于情绪障碍或智力发育迟缓的青少年。我们报告了美国最年轻的长发公主综合征病例,一名5岁智力发育迟缓女童,表现为腹痛、呕吐和无压痛的腹部肿块。

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