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[长发公主综合征——病例报告:毛发石作为肠穿孔的原因]

[The Rapunzel syndrome - a case report: trichobezoar as a cause of intestinal perforation].

作者信息

Faria A P, Silva I Z, Santos A, Avilla S G, Silveira A E

机构信息

Pontifícia Universidade Católica do Paraná (PUC/PR), Curitiba, PR, Brazil.

出版信息

J Pediatr (Rio J). 2000 Jan-Feb;76(1):83-6. doi: 10.2223/jped.806.

Abstract

OBJECTIVE

To report a rare case of a patient with gastric trichobezoar extended through the small bowel, proper to the Rapunzel syndrome. CASE REPORT: Girl at age 7 with history and exams suggestive of peritonitis whose laparotomy demonstrated trichobezoar and jejunal perforation. She also presented alopecia and psychological disorder which were not totally eliminated despite the support given. CONCLUSION: A multidisciplinary view of the patient would have increased the suspicion rate for the pathology and would provide early diagnosis and treatment before complication was evident.

摘要

目的

报告一例罕见的胃毛石延伸至小肠的病例,符合长发公主综合征。病例报告:一名7岁女孩,有腹膜炎病史及相关检查提示,剖腹探查显示有毛石和空肠穿孔。她还伴有脱发和心理障碍,尽管给予了支持,但这些症状并未完全消除。结论:对该患者采用多学科视角本可提高对该病理状况的怀疑率,并在并发症明显之前提供早期诊断和治疗。

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