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长发公主综合征:关于误导性尾巴的隐秘故事。

Rapunzel Syndrome: A Concealed Tale of the Misleading Tail.

作者信息

Kumar Deepak, Pandey Vaibhav, Nandan Ruchira

机构信息

Department of Pediatric Surgery, IMS, Banaras Hindu University, Varanasi, Uttar Pradesh, India.

出版信息

J Indian Assoc Pediatr Surg. 2023 Jan-Feb;28(1):69-71. doi: 10.4103/jiaps.jiaps_86_22. Epub 2023 Jan 10.

DOI:10.4103/jiaps.jiaps_86_22
PMID:36910287
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9997584/
Abstract

The diagnosis of Rapunzel syndrome can sometimes be challenging. The silent features such as poor appetite, constipation, anemia, hypoalbuminemia, and hypoproteinemia were all overlooked in our patient initially. The Rapunzel tail leads to multiple intussusceptions and an unexpected perforation sealed by intussusceptions. Perforation sealed by intussusceptions in a clinically stable patient of Rapunzel syndrome has never been reported.

摘要

长发公主综合征的诊断有时具有挑战性。我们的患者最初忽视了一些隐匿的特征,如食欲不振、便秘、贫血、低白蛋白血症和低蛋白血症。长发公主综合征的尾巴会导致多处肠套叠以及由肠套叠封闭的意外穿孔。临床稳定的长发公主综合征患者中出现由肠套叠封闭的穿孔此前从未有过报道。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/24a9/9997584/d31bddb11f09/JIAPS-28-69-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/24a9/9997584/cccca7016d1a/JIAPS-28-69-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/24a9/9997584/d31bddb11f09/JIAPS-28-69-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/24a9/9997584/cccca7016d1a/JIAPS-28-69-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/24a9/9997584/d31bddb11f09/JIAPS-28-69-g002.jpg

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Cureus. 2024 May 29;16(5):e61294. doi: 10.7759/cureus.61294. eCollection 2024 May.
2
Rapunzel syndrome in children: a retrospective review of ten cases combined with literature review in a tertiary referral center.儿童拉佩尔综合征:一家三级转诊中心回顾性分析十例病例并结合文献复习
Pediatr Surg Int. 2024 May 4;40(1):121. doi: 10.1007/s00383-024-05705-0.

本文引用的文献

1
Rapunzel Syndrome in a 3-Year-Old Boy: A Menace too Early to Present.一名3岁男孩的长发公主综合征:一种过早出现的威胁。
J Indian Assoc Pediatr Surg. 2020 Mar-Apr;25(2):112-114. doi: 10.4103/jiaps.JIAPS_1_19. Epub 2020 Jan 28.
2
Surgical outcome of jejunum-jejunum intussusception secondary to Rapunzel syndrome: a case report.长发公主综合征继发空肠-空肠套叠的手术结果:一例报告
J Med Case Rep. 2018 Dec 7;12(1):362. doi: 10.1186/s13256-018-1883-9.
3
Respiratory arrest due to airway obstruction following endoscopic removal of Trichobezoar.
内镜下取出毛粪石后因气道阻塞导致呼吸骤停。
J Pak Med Assoc. 2011 Jul;61(7):700-1.
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.