• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利：CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法，用中文像聊天一样搜索，搜遍4000万医学文献。AI智能推荐，让科研检索更轻松。

立即免费搜索

文件翻译

保留排版，准确专业，支持PDF/Word/PPT等文件格式，支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述，25分钟生成高质量综述，智能提取关键信息，辅助科研写作。

立即免费体验

长发公主综合征的诊断与治疗

The diagnosis and treatment of Rapunzel syndrome.

作者信息

Wang Zhe, Cao Feng, Liu Diangang, Fang Yu, Li Fei

机构信息

Department of General Surgery, Xuanwu Hospital, Capital Medical University, Beijing, PR China.

出版信息

Acta Radiol Open. 2016 Nov 22;5(11):2058460115627660. doi: 10.1177/2058460115627660. eCollection 2016 Nov.

DOI:10.1177/2058460115627660
PMID:27900201
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5122172/
Abstract

Trichobezoars are hairballs or hair-like fibers formed by chewing and swallowing hair or any other indigestible materials. Trichobezoars usually form in the gastric body and are thus prepyloric. However, trichobezoars may rarely pass through the pylorus into the duodenum, jejunum, ileum, and even the colon, in a condition referred to as Rapunzel syndrome. Here, we present a case of a 13-year-old girl with this rare syndrome and discuss the diagnosis and treatment of the disease.

摘要

毛粪石是由咀嚼并吞咽毛发或任何其他难以消化的物质形成的毛球或毛发样纤维。毛粪石通常在胃体形成，因此位于幽门前。然而，毛粪石很少会通过幽门进入十二指肠、空肠、回肠，甚至结肠，这种情况被称为长发公主综合征。在此，我们报告一例患有这种罕见综合征的13岁女孩病例，并讨论该疾病的诊断和治疗。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a557/5122172/ceb5ed1240db/10.1177_2058460115627660-fig5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a557/5122172/c701917eff1e/10.1177_2058460115627660-fig1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a557/5122172/adc9df4b79b2/10.1177_2058460115627660-fig2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a557/5122172/5f30fcc295a0/10.1177_2058460115627660-fig3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a557/5122172/aafed13be7ed/10.1177_2058460115627660-fig4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a557/5122172/ceb5ed1240db/10.1177_2058460115627660-fig5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a557/5122172/c701917eff1e/10.1177_2058460115627660-fig1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a557/5122172/adc9df4b79b2/10.1177_2058460115627660-fig2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a557/5122172/5f30fcc295a0/10.1177_2058460115627660-fig3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a557/5122172/aafed13be7ed/10.1177_2058460115627660-fig4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a557/5122172/ceb5ed1240db/10.1177_2058460115627660-fig5.jpg

相似文献

1
The diagnosis and treatment of Rapunzel syndrome.长发公主综合征的诊断与治疗
Acta Radiol Open. 2016 Nov 22;5(11):2058460115627660. doi: 10.1177/2058460115627660. eCollection 2016 Nov.
2
Recurrent Rapunzel syndrome - A rare tale of a hairy tail.复发性长发公主综合征——一个关于毛尾巴的罕见故事。
Int J Surg Case Rep. 2018;45:83-86. doi: 10.1016/j.ijscr.2018.03.017. Epub 2018 Mar 21.
3
[Trichobezoar-Rapunzel syndrome--case report].[毛粪石-长发公主综合征——病例报告]
Rozhl Chir. 2004 Sep;83(9):460-2.
4
A Giant Trichobezoar Causing Rapunzel Syndrome in a 12-year-old Female.一例导致12岁女性患长发公主综合征的巨大毛粪石
Indian J Psychol Med. 2011 Jan;33(1):77-9. doi: 10.4103/0253-7176.85401.
5
Recurrent Rapunzel syndrome.复发性 Rapunzel 综合征。
Singapore Med J. 2011 Jun;52(6):e128-30.
6
Rapunzel syndrome due to ingested hair extensions: Surgical and psychiatric considerations.因摄入接发导致的长发公主综合征：手术及精神科方面的考量
Int J Surg Case Rep. 2015;17:155-7. doi: 10.1016/j.ijscr.2015.11.009. Epub 2015 Nov 19.
7
A rare variant of rapunzel syndrome-acute small bowel obstruction caused by ball of hairs in distal ileum with its tail extending in caecum and ascending colon.拉庞泽尔综合征的一种罕见变体——急性小肠梗阻，由回肠末端的毛球引起，其尾部延伸至盲肠和升结肠。
J Pak Med Assoc. 2016 Jun;66(6):761-4.
8
Fatal Rapunzel Syndrome: Gastric and Intestinal Trichobezoars in a Child With Trichotillomania.致命的长发公主综合征：一名拔毛癖儿童的胃和肠道毛发石
Am J Forensic Med Pathol. 2023 Sep 1;44(3):210-215. doi: 10.1097/PAF.0000000000000849. Epub 2023 Jun 5.
9
A rare outcome of iron deficiency and pica: Rapunzel syndrome in a 5-year-old child iron deficiency and pica.缺铁和异食癖的罕见后果：一名5岁儿童患长发公主综合征与缺铁和异食癖。
Turk J Gastroenterol. 2014 Feb;25(1):100-2. doi: 10.5152/tjg.2014.4051.
10
Rapunzel syndrome: a rare form of trichobezoar in the stomach with some extension into the small intestine.长发公主综合征：一种罕见的胃内毛石症，部分延伸至小肠。
Acta Dermatovenerol Alp Pannonica Adriat. 2018 Sep;27(3):155-157.

引用本文的文献

1
Rapunzel Syndrome: Clinical, Diagnostic and Forensic Aspects in Related Deaths-A Review of the Literature.长发公主综合征：相关死亡的临床、诊断及法医方面——文献综述
J Clin Med. 2024 Dec 8;13(23):7464. doi: 10.3390/jcm13237464.
2
Rapunzel Syndrome: Diagnostic Challenges and Multidisciplinary Treatment Strategies.长发公主综合征：诊断挑战与多学科治疗策略
Cureus. 2024 May 29;16(5):e61294. doi: 10.7759/cureus.61294. eCollection 2024 May.
3
Gastrointestinal Bezoars in Paediatrics: Case Series and Literature Review.儿科胃石症：病例系列及文献复习。

本文引用的文献

1
The surgical management of Rapunzel syndrome: a case series and literature review.Rapunzel 综合征的外科治疗：病例系列和文献复习。
J Pediatr Surg. 2013 Apr;48(4):830-4. doi: 10.1016/j.jpedsurg.2012.07.046.
2
Endoscopic retrieval of a gastric trichobezoar.内镜下取出胃内毛发石。
World J Gastrointest Endosc. 2011 Jan 16;3(1):20-2. doi: 10.4253/wjge.v3.i1.20.
3
Laparoscopic intragastric removal of giant trichobezoar.腹腔镜下胃内巨大毛石的取出术
Afr J Paediatr Surg. 2024 Apr 1;21(2):101-106. doi: 10.4103/ajps.ajps_104_22. Epub 2023 Feb 14.
4
Gastrointestinal trichobezoars in the pediatric population: a retrospective study.儿童人群中的胃肠道毛粪石：一项回顾性研究。
BMC Pediatr. 2024 Feb 16;24(1):124. doi: 10.1186/s12887-023-04489-x.
5
Rapunzel syndrome complicated with pancreatitis, intussusception and intestinal perforation.雷朋泽尔综合征合并胰腺炎、肠套叠和肠穿孔。
BMJ Case Rep. 2022 Jul 4;15(7):e247005. doi: 10.1136/bcr-2021-247005.
6
A huge abdominal mass revealing a depressive syndrome.腹部巨大肿块致抑郁综合征。
Ann R Coll Surg Engl. 2021 Mar;103(3):e77-e80. doi: 10.1308/rcsann.2020.7093.
7
Trichobezoar as a cause of pediatric acute small bowel obstruction.毛发石作为小儿急性小肠梗阻的一个病因
Clin Case Rep. 2019 Dec 18;8(1):166-170. doi: 10.1002/ccr3.2576. eCollection 2020 Jan.
8
Rapunzel syndrome: a tail too long to tell!长发公主综合征：一条长得离谱的尾巴！
BMJ Case Rep. 2018 Apr 5;2018:bcr-2018-224756. doi: 10.1136/bcr-2018-224756.
JSLS. 2010 Apr-Jun;14(2):259-62. doi: 10.4293/108680810X12785289144520.
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
Laparoscopic removal of a large gastric trichobezoar in a 4-year-old girl.4岁女童腹腔镜下取出巨大胃毛石
JSLS. 2009 Oct-Dec;13(4):608-11. doi: 10.4293/108680809X12589999538110.
6
Laparoscopic removal of a gastric trichobezoar in a pediatric patient.小儿患者胃内毛石的腹腔镜切除术
J Laparoendosc Adv Surg Tech A. 2009 Dec;19(6):835-7. doi: 10.1089/lap.2008.0367.
7
Clinical characteristics of trichotillomania with trichophagia.拔毛癖伴食毛症的临床特征
Compr Psychiatry. 2008 Nov-Dec;49(6):579-84. doi: 10.1016/j.comppsych.2008.05.002. Epub 2008 Aug 23.
8
Rapunzel syndrome: the unsuspected culprit.长发公主综合征：意想不到的罪魁祸首。
World J Gastroenterol. 2008 Feb 21;14(7):1141-3. doi: 10.3748/wjg.14.1141.
9
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.
10
Large gastric trichobezoar in a normal healthy woman: case report and review of pertinent literature.一名健康正常女性体内的巨大胃毛石：病例报告及相关文献综述
South Med J. 2005 Oct;98(10):1042-4. doi: 10.1097/01.smj.0000182175.55032.4a.