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[长发公主综合征作为梗阻和肠穿孔的原因]

[Rapunzel syndrome as a cause of obstruction and intestinal perforation].

作者信息

Rojas Patricia Guzmán, Paredes Eduar Bravo, Reto Catherina Pichilingue

出版信息

Acta Gastroenterol Latinoam. 2016 Jun;46(2):114-7.

Abstract

The following is a case report involving a 16 year old female with trichotillomania as an antecedent. This patient presented to the Emergency Room with a chief complaint of early satiety and persistent abdominal pain for the past 3 months. However, recently her abdominal pain has worsened and it is now complicated by nausea and vomiting. The physical exam was notable for epigastric pain on deep palpation. The biochemical analysis and abdominal ultrasound were otherwise unremarkable. An esophagogastroduodenoscopy was subsequently performed where a trichobezoar was discovered. It extended from the gastric fundus to the third portion of the duodenum. A surgical extraction of the trichobezoar was then performed. The trichobezoar was found to be 130 cm in length and 8 cm wide at its most cephalad aspect. It is important to note that they also found five mall perforations throughout the duodenum and jejunum. The patient was discharged with outpatient follow up with psychiatry. In this report we describe the case of a patient with Rapunzel syndrome that was complicated by small bowel perforation and we provide a review of the salient literature concerning this syndrome and its associated complications.

摘要

以下是一份病例报告,涉及一名16岁患有拔毛癖的女性。该患者因过去3个月出现早饱感和持续性腹痛为主诉前往急诊室就诊。然而,最近她的腹痛加重,现在并发恶心和呕吐。体格检查发现深触诊时上腹部疼痛。生化分析和腹部超声检查未见异常。随后进行了食管胃十二指肠镜检查,发现了一个毛石。它从胃底延伸至十二指肠第三部分。然后对毛石进行了手术摘除。发现毛石长度为130厘米,最上端宽8厘米。需要注意的是,他们还在整个十二指肠和空肠发现了五个小穿孔。患者出院后接受精神科门诊随访。在本报告中,我们描述了一例并发小肠穿孔的长发公主综合征患者的病例,并对有关该综合征及其相关并发症的重要文献进行了综述。

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