| Literature DB >> 29057712 |
Islam Nour1, Mona Abd Alatef1, Ahmed Megahed1, Sohier Yahia1, Yahya Wahba1, Abd Elazeez Shabaan1.
Abstract
Rapunzel syndrome is a rare form of gastric trichobezoar. A 4-year-old girl presented with generalised oedema and an epigastric mass. Her family was of a relatively low socio-economic background. There was microcytic hypochromic anaemia, hypoalbuminaemia and an elevated α1-antitrypsin clearance. Abdominal ultrasound and non-contrast computed tomography demonstrated a heterogeneous mass related to the stomach. Upper gastro-intestinal tract endoscopy failed to remove it. Surgical laparotomy was undertaken through a single anterior gastrotomy incision and a large mass was extracted which was a cast of the duodenum and stomach and had a tail of approximately 60 cm in length which extended to the jejunum. Low socio-economic status, child neglect and pica are risk factors for trichobezoars. Surgical laparotomy is the optimal treatment of large bezoars.Entities:
Keywords: Egyptian; Oedema; Rapunzel syndrome; endoscopy; epigastric; laparotomy; trichobezoars
Mesh:
Year: 2017 PMID: 29057712 DOI: 10.1080/20469047.2017.1389809
Source DB: PubMed Journal: Paediatr Int Child Health ISSN: 2046-9047 Impact factor: 1.990