Naik Saleem, Gupta Vivek, Naik Swati, Rangole Ashwin, Chaudhary Ashok K, Jain Prashant, Sharma Ashok K
Department of Surgery, Pandit Jawahar Lal Nehru Medical College, Raipur, and Department of Surgical Gastroenterology, Bhopal Memorial Hospital, India.
Dig Surg. 2007;24(3):157-61. doi: 10.1159/000102098. Epub 2007 Apr 27.
Rapunzel syndrome is a rare presentation of a trichobezoar, with 24 cases having been reported in literature so far. This syndrome has been reported in 23 female and 1 male patient with a mean age of 10.8 years. The patients commonly present with abdominal pain, nausea, vomiting and signs of obstruction. The distal end of the bezoar may be in the jejunum, ileum or the colon. We evaluate the various cases reported and discuss the various modes of presentation of this uncommon syndrome, and also present a series of 3 cases, all females, aged 16, 18 and 21 years, and had a trichobezoar in the stomach with a tail extending into the ileum.
长发公主综合征是毛粪石的一种罕见表现,迄今为止文献中已报道24例。该综合征已在23名女性和1名男性患者中报道,平均年龄为10.8岁。患者通常表现为腹痛、恶心、呕吐及梗阻体征。粪石远端可能位于空肠、回肠或结肠。我们评估了已报道的各种病例,讨论了这种罕见综合征的各种表现形式,并呈现了一组3例病例,均为女性,年龄分别为16岁、18岁和21岁,胃内有毛粪石且尾部延伸至回肠。