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长发公主尾巴的曲折故事：以脱落的女儿胃石作为肠套叠的起始点

A Convoluted Tale of Rapunzel Tail: With Dislodged Daughter Bezoar as Lead Point for Intussusception.

作者信息

Mathew Priya, Singh Aditya Pratap, Mittal Priyanka, Mathur Praveen

机构信息

Department of Pediatric Surgery, Sawai Man Singh Medical College, Jaipur, Rajasthan, India.

出版信息

Int J Trichology. 2024 Jan-Dec;16(1-6):42-44. doi: 10.4103/ijt.ijt_70_21. Epub 2025 Apr 18.

DOI:10.4103/ijt.ijt_70_21
PMID:40309375
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC12039773/
Abstract

Rapunzel syndrome (RS) can have a varied clinical presentation, spanning from being asymptomatic to having a fatal outcome. If left untreated, complications are inevitable. This case highlights an amalgamation of varied presentations of RS with a daughter bezoar acting as a lead point for intussusception, its management, and favorable result. The purpose of this discussion is to throw the focus on the blend of diverse clinical findings and complications of RS with a daughter bezoar; and the importance of early surgical intervention followed by psychological support and psychiatric treatment, as a key to a successful outcome.

摘要

长发公主综合征（RS）的临床表现多样，从无症状到出现致命后果不等。若不治疗，并发症不可避免。本病例突出了RS多种表现形式与作为肠套叠起始点的胃石合并出现的情况、其治疗及良好结果。本次讨论的目的是聚焦RS的各种临床发现及并发症与胃石的混合情况；以及早期手术干预并随后给予心理支持和精神治疗作为取得成功结果关键的重要性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/80f9/12039773/2911e929b107/IJT-16-42-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/80f9/12039773/95ec3d547261/IJT-16-42-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/80f9/12039773/2911e929b107/IJT-16-42-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/80f9/12039773/95ec3d547261/IJT-16-42-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/80f9/12039773/2911e929b107/IJT-16-42-g002.jpg

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Int J Trichology. 2024 Jan-Dec;16(1-6):42-44. doi: 10.4103/ijt.ijt_70_21. Epub 2025 Apr 18.
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The Rapunzel syndrome. Report of a case and review of the literature.长发公主综合征。一例报告及文献综述。
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本文引用的文献

1
A hairy situation: trichobezoar presenting with intussusception, and intestinal and biliary perforation in a child.棘手的情况：一名儿童出现毛粪石伴肠套叠、肠道及胆道穿孔
Radiol Case Rep. 2016 Dec 3;12(1):42-44. doi: 10.1016/j.radcr.2016.07.003. eCollection 2017 Mar.
2
Rapunzel syndrome presenting as jejuno-jejunal intussusception.表现为空肠-空肠套叠的长发公主综合征。
Clin J Gastroenterol. 2015 Aug;8(4):202-6. doi: 10.1007/s12328-015-0578-7. Epub 2015 Jun 25.
3
An unusual case report of rapunzel syndrome trichobezoar in a 3-year-old boy.
一名3岁男孩患长发公主综合征毛粪石的罕见病例报告。
Int J Trichology. 2011 Jul;3(2):102-4. doi: 10.4103/0974-7753.90820.
4
Management of trichobezoar: case report and literature review.毛发石的管理：病例报告与文献综述
Pediatr Surg Int. 2010 May;26(5):457-63. doi: 10.1007/s00383-010-2570-0. Epub 2010 Mar 6.
5
Rapunzel syndrome reviewed and redefined.长发公主综合征的回顾与重新定义。
Dig Surg. 2007;24(3):157-61. doi: 10.1159/000102098. Epub 2007 Apr 27.
6
The Rapunzel syndrome (trichobezoar) causing atypical intussusception in a child: a case report.导致儿童非典型肠套叠的长发公主综合征（毛粪石）：一例报告
J Pediatr Surg. 1999 Mar;34(3):479-80. doi: 10.1016/s0022-3468(99)90504-3.
7
An unusual case of the trichobezoar: the Rapunzel syndrome.一例罕见的毛粪石病例：长发公主综合征。
Am J Gastroenterol. 1982 Jul;77(7):467-70.
8
The Rapunzel syndrome. An unusual complication of intestinal bezoar.长发公主综合征。一种罕见的肠粪石并发症。
Surgery. 1968 Feb;63(2):339-43.