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[长发公主综合征一例]

[A case of Rapunzel syndrome].

作者信息

Eryilmaz Ramazan, Sahin Mustafa, Alimoğlu Orhan, Yildiz M Kamil

机构信息

1st Department of General Surgery, SSK Vakif Gureba Training Hospital, Istanbul, Turkey.

出版信息

Ulus Travma Acil Cerrahi Derg. 2004 Oct;10(4):260-3.

Abstract

Trichobezoars are concretions of hair casts in the stomach associated with trichotillomania and trichophagia. The condition is termed Rapunzel syndrome when formation of a huge trichobezoar extends to the small bowel, resulting in gastrointestinal obstruction. We present a 19-year-old girl who had complaints of colicky abdominal pain, nausea and vomiting seven years after surgical treatment for a gastric trichobezoar. Gastric endoscopy was performed with an initial diagnosis of recurrent trichobezoar, which revealed a huge one. The patient underwent laparotomy, during which a huge trichobezoar with a long tail was totally removed by an anterior gastrotomy. Following removal of the lesion, the antrum was observed with multiple ulcers secondary to extensive pressure. Postoperative period was uneventful. A subsequent psychiatric consultation revealed depressive personality disorder.

摘要

胃石是胃内毛发团块,与拔毛癖和食毛癖有关。当巨大胃石形成并延伸至小肠导致胃肠道梗阻时,这种情况被称为长发公主综合征。我们报告一名19岁女孩,她在接受胃石手术治疗7年后出现绞痛性腹痛、恶心和呕吐。最初诊断为复发性胃石而行胃镜检查,发现一个巨大胃石。患者接受剖腹手术,术中通过前胃切开术将一个带长尾的巨大胃石完全切除。切除病变后,观察到胃窦有多处因广泛压迫继发的溃疡。术后恢复顺利。随后的精神科会诊显示为抑郁型人格障碍。

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