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1
Extremely unusual case of gastrointestinal trichobezoar.极其罕见的胃肠道毛粪石病例。
World J Clin Cases. 2015 May 16;3(5):466-9. doi: 10.12998/wjcc.v3.i5.466.
2
Giant gastric trichobezoar in a young female with Rapunzel syndrome: case report.一名患有长发公主综合征的年轻女性的巨大胃毛石:病例报告。
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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。
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Rapunzel Syndrome in a Teenage Girl: A Case Report.一名少女的长发公主综合征:病例报告
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引用本文的文献

1
Atypical Rapunzel Syndrome in an Adult Female: Trichobezoar Beyond the Gastric Outlet Leading to Gastrointestinal Perforation and Septic Shock.成年女性的非典型长发公主综合征:胃出口以外的毛石导致胃肠道穿孔和感染性休克。
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Coexistence of bezoar and superior mesenteric artery syndrome: A case report.胃石与肠系膜上动脉综合征并存:一例报告。
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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.
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[Rapunzel syndrome: Radiological diagnosis].[长发公主综合征:影像学诊断]
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5
A 'Hairy' problem: Trichotillomania, trichophagia and trichobezoars.一个“棘手”的问题:拔毛癖、食毛癖和毛粪石。
Singapore Med J. 2016 Jul;57(7):411. doi: 10.11622/smedj.2016125.
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.

本文引用的文献

1
Laparoscopic-assisted removal of gastric trichobezoar; a novel technique to reduce operative complications and time.腹腔镜辅助下胃毛粪石取出术;一种降低手术并发症和时间的新方法。
J Pediatr Surg. 2013 Mar;48(3):e13-5. doi: 10.1016/j.jpedsurg.2012.12.028.
2
Unusual cause of palpable mass in upper abdomen--giant gastric trichobezoar: report of a case.上腹部可触及肿块的罕见病因——巨大胃毛石:1例报告
Acta Chir Belg. 2012 Mar-Apr;112(2):160-3. doi: 10.1080/00015458.2012.11680816.
3
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.
4
Trichotillomania: A current review.拔毛癖:最新综述。
Clin Psychol Rev. 2010 Mar;30(2):181-93. doi: 10.1016/j.cpr.2009.10.008. Epub 2009 Oct 30.
5
Rapunzel syndrome: a comprehensive review of an unusual case of trichobezoar.长发公主综合征:一例罕见毛粪石病例的全面综述
Clin Med Res. 2009 Sep;7(3):99-102. doi: 10.3121/cmr.2009.822. Epub 2009 Jul 22.
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
Common and unique factors associated with DSM-IV-TR internalizing disorders in children.与儿童DSM-IV-TR内化性障碍相关的常见因素和独特因素。
J Abnorm Child Psychol. 2008 Nov;36(8):1279-88. doi: 10.1007/s10802-008-9250-8.
8
Successful treatment with a combination of endoscopic injection and irrigation with coca cola for gastric bezoar-induced gastric outlet obstruction.内镜注射联合可口可乐冲洗成功治疗胃石症所致胃出口梗阻。
J Chin Med Assoc. 2008 Jan;71(1):49-52. doi: 10.1016/S1726-4901(08)70073-X.
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
Trichotillomania and trichobezoar: a clinical practice insight with report of illustrative case.拔毛癖与毛发石:临床实践见解及病例报告
J Am Osteopath Assoc. 2006 Nov;106(11):647-52.

极其罕见的胃肠道毛粪石病例。

Extremely unusual case of gastrointestinal trichobezoar.

作者信息

Jatal Sopan N, Jamadar Nawab P, Jadhav Bhagwat, Siddiqui Saleha, Ingle Sachin B

机构信息

Sopan N Jatal, Jatal Hospital and Research Centre Latur, Maharashtra 4132512, India.

出版信息

World J Clin Cases. 2015 May 16;3(5):466-9. doi: 10.12998/wjcc.v3.i5.466.

DOI:10.12998/wjcc.v3.i5.466
PMID:25984522
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4419111/
Abstract

Trichobezoars (hair ball) are usually located in the stomach, but may extend through the pylorus into the duodenum and small bowel (Rapunzel syndrome). Rapunzel syndrome remains uncommon; with fewer than 40 cases reported. To the best of our knowledge, this case may be the first well-documented case with a length of 75 cm. They are almost always associated with trichotillomania and trichophagia or other psychiatric disorders. In the literature several treatment options are proposed, including removal by conventional laparotomy, laparoscopy and endoscopy. Herein, we are reporting an interesting case of an 18-year mentally retarded girl with history of trichotillomania and trichophagia who presented to our emergency department with a history of central abdominal pain associated with vomiting and constipation for five days. An examination showed a trichobezoar requiring emergent surgical intervention, and indicating the need for psychiatric treatment. The trichobezoar was treated successfully by laparoscopy.

摘要

胃石(毛球)通常位于胃内,但可能通过幽门延伸至十二指肠和小肠(长发公主综合征)。长发公主综合征仍然不常见,报告的病例少于40例。据我们所知,该病例可能是首例有详细记录、长度达75厘米的病例。它们几乎总是与拔毛癖和食毛癖或其他精神障碍相关。文献中提出了几种治疗选择,包括传统剖腹手术、腹腔镜手术和内窥镜检查。在此,我们报告一例有趣的病例,一名18岁智力发育迟缓女孩,有拔毛癖和食毛癖病史,因中腹部疼痛伴呕吐和便秘5天就诊于我们的急诊科。检查发现一个需要紧急手术干预的胃石,同时表明需要进行精神治疗。该胃石通过腹腔镜手术成功治疗。