Michael E. DeBakey Department of Surgery, Division of Pediatric Surgery, Baylor College of Medicine, Houston, TX 77030, USA.
J Pediatr Surg. 2013 Apr;48(4):830-4. doi: 10.1016/j.jpedsurg.2012.07.046.
BACKGROUND/PURPOSE: The surgical removal of a trichobezoar is the rare end complication of the psychiatric disorders trichotillomania and trichophagia. The more severe form of the disease is termed Rapunzel syndrome, where the bezoar extends from the gastric body beyond the pylorus into the duodenum. Traditional therapy has included endoscopy, often with subsequent laparotomy, and associated psychiatric intervention. We present the largest and most recent series of patients with trichobezoars managed in a single institution.
A retrospective review of all cases of trichobezoar at our institution from 2003 to 2011 was performed. Demographic data, presenting complaints, imaging, surgical treatment, and subsequent management were collected.
All 7 patients were female, ages 5 to 23 years (mean, 11.5 years). Although multiple imaging modalities were necessary for preoperative diagnosis, most patients were accurately diagnosed without endoscopic evaluation (85%). All patients required an exploratory laparotomy for definitive treatment. At laparotomy, 5 patients were found to have postpyloric extension of the trichobezoar (71%). One of 7 patients had a wound infection postoperatively. There were no other surgical complications or recurrences requiring further exploration.
Our series of trichobezoar patients appear to have a high rate of Rapunzel syndrome, and perhaps postpyloric extension should be considered the rule rather than the exception. Our series demonstrates that diagnosis can be established with a thorough history combined with radiography, and treatment should be a combination of laparoscopy and/or laparotomy with psychiatric consultation.
背景/目的:毛粪石是拔毛癖和异食癖等精神障碍的罕见手术并发症。该病的更严重形式被称为长发公主综合征,此时毛粪石从胃体延伸超过幽门进入十二指肠。传统的治疗方法包括内镜检查,通常随后进行剖腹手术,并进行相关的精神干预。我们报告了在单一机构中管理的最大和最新的一组毛粪石患者系列。
对我们机构 2003 年至 2011 年期间所有毛粪石病例进行回顾性研究。收集人口统计学数据、临床表现、影像学、手术治疗和后续管理。
所有 7 例患者均为女性,年龄 5 至 23 岁(平均 11.5 岁)。尽管术前诊断需要多种影像学方法,但大多数患者无需内镜评估即可准确诊断(85%)。所有患者均需要剖腹探查以进行明确治疗。剖腹探查时,发现 5 例患者的毛粪石延伸至幽门后(71%)。7 例患者中有 1 例术后出现伤口感染。无其他手术并发症或需要进一步探查的复发。
我们的毛粪石患者系列似乎有很高的长发公主综合征发生率,也许幽门后延伸应该被认为是常规而非例外。我们的系列表明,通过详细的病史结合放射学可以确立诊断,治疗应结合腹腔镜和/或剖腹手术以及精神科咨询。