• 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

导致儿童胃穿孔的长发公主综合征(毛粪石):一例报告

The Rapunzel syndrome (trichobezoar) causing gastric perforation in a child: a case report.

作者信息

Pul N, Pul M

机构信息

Cocuk Sağliği ve Hastaliklari Uzmani, Edirne, Turkey.

出版信息

Eur J Pediatr. 1996 Jan;155(1):18-9. doi: 10.1007/BF02115620.

DOI:10.1007/BF02115620
PMID:8750804
Abstract

UNLABELLED

The Rapunzel syndrome (RS), is a rare form of gastric trichobezoar extending throughout the bowel. We report on a patient with RS causing gastric perforation and discuss the aetiology, pathogenesis, diagnosis and treatment of this unusual syndrome. RS is found characteristically in girls with varying gastro-intestinal symptoms. The recommended treatment for large or complicated trichobezoars is surgery. Psychiatric follow up is essential to diminish the frequency of recurrence.

CONCLUSION

Symptoms of trichobezoars are nonspecific and may mimic those of other pathological gastro-intestinal conditions. Early diagnosis and treatment of this condition is of prime importance and may avoid later fatal complications.

摘要

未标注

长发公主综合征(RS)是一种罕见的胃内毛石症,可延伸至整个肠道。我们报告一例因RS导致胃穿孔的患者,并讨论这种罕见综合征的病因、发病机制、诊断和治疗。RS典型地见于有各种胃肠道症状的女孩。对于大的或复杂的毛石症,推荐的治疗方法是手术。进行精神科随访对于减少复发频率至关重要。

结论

毛石症的症状不具特异性,可能与其他病理性胃肠道疾病的症状相似。对这种疾病进行早期诊断和治疗至关重要,可避免后期出现致命并发症。

相似文献

1
The Rapunzel syndrome (trichobezoar) causing gastric perforation in a child: a case report.导致儿童胃穿孔的长发公主综合征(毛粪石):一例报告
Eur J Pediatr. 1996 Jan;155(1):18-9. doi: 10.1007/BF02115620.
2
Trichobezoar causing recurrent gastric ulcer and perforation.毛粪石导致复发性胃溃疡和穿孔。
Wien Klin Wochenschr. 2015 Jan;127(1-2):16. doi: 10.1007/s00508-014-0607-4. Epub 2014 Sep 19.
3
An unusual cause of gastric perforation in childhood: trichobezoar (Rapunzel syndrome). A case report.儿童胃穿孔的罕见病因:毛发石(长发公主综合征)。病例报告。
Eur J Pediatr. 2009 Apr;168(4):495-7. doi: 10.1007/s00431-008-0773-3. Epub 2008 Jun 12.
4
A Case Report: Large Trichobezoar Causing Rapunzel Syndrome.病例报告:巨大毛粪石导致长发公主综合征。
Medicine (Baltimore). 2016 May;95(22):e3745. doi: 10.1097/MD.0000000000003745.
5
[The Rapunzel syndrome: rare manifestation of a trichobezoar of the upper gastrointestinal tract].[长发公主综合征:上消化道毛粪石的罕见表现]
Chirurg. 2003 Aug;74(8):753-6. doi: 10.1007/s00104-003-0680-0.
6
Rapunzel syndrome complicated with gastric perforation diagnosed on operation table.手术台上诊断为长发公主综合征合并胃穿孔。
J Gastrointest Surg. 2008 Dec;12(12):2240-2. doi: 10.1007/s11605-007-0460-0. Epub 2008 Jan 3.
7
Rapunzel and pregnancy.长发公主与怀孕。
South Med J. 2009 Jan;102(1):106-7. doi: 10.1097/SMJ.0b013e31818987b9.
8
Trichobezoar causing pancreatitis: first reported case of Rapunzel syndrome in a boy in North America.毛发粪石导致胰腺炎:北美首例男孩版“长发公主综合征”病例报告。
J Pediatr Surg. 2012 Mar;47(3):e17-9. doi: 10.1016/j.jpedsurg.2011.11.002.
9
[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.
10
Duodenal diastatic perforation due to double gastric and jejunal trichobezoar in a patient with Rapunzel syndrome.Rapunzel 综合征患者因双重胃和空肠毛粪石导致十二指肠消化性穿孔。
Rev Esp Enferm Dig. 2023 Apr;115(4):222-223. doi: 10.17235/reed.2023.9394/2022.

引用本文的文献

1
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.
2
Therapeutic Upper Gastrointestinal Endoscopy in Pediatric Gastroenterology.儿科胃肠病学中的治疗性上消化道内镜检查
Front Pediatr. 2022 Feb 25;9:715912. doi: 10.3389/fped.2021.715912. eCollection 2021.
3
Huge trichobezoar presenting as abdominal mass and weight loss: Case report.

本文引用的文献

1
The Rapunzel syndrome: a case report and review of the literature.长发公主综合征:一例病例报告及文献综述
Eur J Pediatr Surg. 1993 Jun;3(3):171-3. doi: 10.1055/s-2008-1063536.
2
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.
3
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。
巨大毛粪石表现为腹部肿块及体重减轻:病例报告
Int J Surg Case Rep. 2019;57:33-35. doi: 10.1016/j.ijscr.2019.02.033. Epub 2019 Mar 7.
4
Rapunzel syndrome is not just a mere surgical problem: A case report and review of current management.长发公主综合征并非仅仅是一个外科问题:一例病例报告及当前治疗方法综述。
World J Clin Cases. 2017 Feb 16;5(2):50-55. doi: 10.12998/wjcc.v5.i2.50.
5
Rapunzel syndrome: a rare cause of hypoproteinaemia and review of literature.长发公主综合征:低蛋白血症的罕见病因及文献综述
BMJ Case Rep. 2016 Sep 26;2016:bcr2016216600. doi: 10.1136/bcr-2016-216600.
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
13-year-old with cryptic abdominal pain.13岁,有不明原因的腹痛。
West J Emerg Med. 2015 Jan;16(1):149-50. doi: 10.5811/westjem.2014.11.24429. Epub 2014 Dec 5.
8
Terminal ileal trichophytobezoar with perforation: A rare presentation with review.伴有穿孔的末端回肠毛粪石:一种罕见表现并文献复习
J Indian Assoc Pediatr Surg. 2008 Jan;13(1):38-40. doi: 10.4103/0971-9261.42575.
9
Trichobezoar presenting with the 'comma sign' in Rapunzel Syndrome: a case report and literature review.长发公主综合征中呈现“逗号征”的毛粪石:一例报告及文献综述
Cases J. 2008 Oct 30;1(1):286. doi: 10.1186/1757-1626-1-286.
10
An unusual cause of gastric perforation in childhood: trichobezoar (Rapunzel syndrome). A case report.儿童胃穿孔的罕见病因:毛发石(长发公主综合征)。病例报告。
Eur J Pediatr. 2009 Apr;168(4):495-7. doi: 10.1007/s00431-008-0773-3. Epub 2008 Jun 12.
Surgery. 1968 Feb;63(2):339-43.
4
Trichobezoar: case presentation and review of literature.毛粪石:病例报告及文献综述
J Am Osteopath Assoc. 1973 Feb;72(6):628-34.
5
Bezoars: classification, pathophysiology, and treatment.胃石:分类、病理生理学及治疗
Am J Gastroenterol. 1988 May;83(5):476-8.