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胃毛石症和长发公主综合征:一种极为罕见病症的病例报告

Gastric trichobezoar and Rapunzel syndrome: case report of a very rare condition.

作者信息

Kouskos E, Polychroni D, Rizou M, Andronikou A, Petrellis V

机构信息

Surgical Department, General Hospital of Mytilene, Lesvos Island, Greece.

Department of Obstetrics and Gynecology, General Hospital of Mytilene, Lesvos Island, Greece.

出版信息

Hippokratia. 2023 Jan-Mar;27(1):25-27.

Abstract

BACKGROUND

Rapunzel syndrome is a rare trichobezoar variant extending from the gastric cavity into the small bowel.

CASE DESCRIPTION

We report the case of a 22-year-old woman who presented with epigastric pain, nausea, and loss of appetite within the preceding five weeks. She had a palpable mass in the epigastric area with mild localized tenderness. Her abdominal computed tomography scan showed a distended stomach and duodenum, with a heterogeneous solid material, suspicious for a bezoar. Upper gastrointestinal endoscopy revealed a large, densely packed trichobezoar occupying the gastric cavity and extending through the pylorus. Endoscopic removal of the bezoar was unsuccessful. The patient underwent a 6cm-long gastrotomy, and the 150cm-long bezoar, extending from the stomach to the jejunum, was uneventfully removed. The patient was referred postoperatively to a dietitian and psychiatrist for management of her trichotillomania and trichophagia.

CONCLUSION

Trichobezoars are commonly found in young females with a history of trichotillomania and trichophagia and are associated with psychiatric disorders. HIPPOKRATIA 2023, 27 (1):25-27.

摘要

背景

长发公主综合征是一种罕见的毛石症变体,从胃腔延伸至小肠。

病例描述

我们报告一例22岁女性病例,该患者在之前五周内出现上腹部疼痛、恶心和食欲不振。她在上腹部区域可触及一个肿块,伴有轻度局部压痛。她的腹部计算机断层扫描显示胃和十二指肠扩张,有一个不均匀的实性物质,怀疑是毛石。上消化道内镜检查发现一个大的、紧密堆积的毛石占据胃腔并延伸至幽门。内镜下取出毛石未成功。患者接受了一个6厘米长的胃切开术,顺利取出了从胃延伸至空肠的150厘米长的毛石。术后患者被转介给营养师和精神科医生,以治疗她的拔毛癖和食毛癖。

结论

毛石常见于有拔毛癖和食毛癖病史的年轻女性,且与精神障碍有关。《希波克拉底》2023年,第27卷(1):25 - 27页。

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