Casey M C, Robertson I, Waters P S, Hanaghan J, Khan W, Barry K
Department of General Surgery, Mayo General Hospital, Ireland.
Department of General Surgery, Mayo General Hospital, Ireland.
Int J Surg Case Rep. 2014;5(3):135-7. doi: 10.1016/j.ijscr.2013.12.024. Epub 2014 Jan 8.
No consensus exists regarding definitive management of colonic perforation in Ehlers-Danlos syndrome (EDS), with various authors advocating different operative techniques. Spontaneous colonic perforation is a recognised complication of vascular-type EDS (type IV), with many reported cases in the literature. No such cases have been reported concerning classical-type EDS (type I/II).
A 55-year-old male with a family history of EDS presented with acute lower abdominal pain and signs of localised peritonitis. Following resuscitation, computerised tomography identified perforation of a sigmoid diverticulum with localised intraperitoneal air. Considering the potential complications associated with laparotomy in a patient with EDS, a trial of conservative management was undertaken including image-guided drainage of a mesenteric abscess. Intensive care monitoring, nutritional support and intravenous antibiotics also facilitated successful non-operative management. Following discharge, molecular studies confirmed COL5A1 mutation, and a diagnosis of classical Ehlers-Danlos syndrome was established.
This is the first reported case of successful conservative management of colonic diverticular perforation in a patient with classical Ehlers-Danlos syndrome.
EDS is highly significant in the surgical context, with the causative genetic factors serving to further complicate the course of surgical intervention. In the absence of consensus regarding best surgical management, due consideration should be given to non-operative management of benign colonic perforation.
关于埃勒斯-当洛斯综合征(EDS)患者结肠穿孔的确切治疗方法尚无共识,不同作者主张不同的手术技术。自发性结肠穿孔是血管型EDS(IV型)公认的并发症,文献中有许多相关病例报道。但关于经典型EDS(I/II型),尚无此类病例报道。
一名有EDS家族史的55岁男性,出现急性下腹痛和局限性腹膜炎体征。复苏后,计算机断层扫描发现乙状结肠憩室穿孔,伴有局限性腹腔内积气。考虑到EDS患者行剖腹手术可能出现的并发症,进行了保守治疗尝试,包括在影像引导下引流肠系膜脓肿。重症监护监测、营养支持和静脉使用抗生素也有助于成功进行非手术治疗。出院后,分子研究证实存在COL5A1突变,确诊为经典型埃勒斯-当洛斯综合征。
这是首例关于经典型埃勒斯-当洛斯综合征患者结肠憩室穿孔成功保守治疗的报道病例。
EDS在外科手术领域具有重要意义,致病基因因素会使手术干预过程更加复杂。在最佳手术治疗方法尚无共识的情况下,应充分考虑对良性结肠穿孔进行非手术治疗。