Fogel Sandy
Department of Surgery, Virginia Tech Carilion School of Medicine, Roanoke, Virginia 24016, USA.
Am Surg. 2013 Jun;79(6):608-13.
Ehlers-Danlos syndrome (EDS) is a closely related group of disorders caused by a heritable defect in collagen synthesis, which leads to marked healing difficulties. It has been estimated to occur in between one in 2500 and one in 5000 individuals but likely occurs more frequently than reported. EDS has probably been seen by all general surgeons several times over the course of a career. The purpose of this report is to describe the findings that should raise the index of suspicion, to aid in the diagnosis, and to characterize the general surgical procedures seen in patients with EDS by reviewing a single surgeon's experience in managing such patients with a review of the literature. Recommendations for treatment are given. A retrospective review of the experience of a single surgeon of 25 procedures in 15 patients with EDS is being reported. This is believed to be the largest series by one surgeon as yet reported. There was a wide variety of procedures performed, including ventral hernia repair (n = 6), inguinal hernia repair (n = 4), colectomy (n = 3), anal fistula (n = 3), and one each of an exploratory laparotomy, an appendectomy, a closure of a dehiscence, a Hickman catheter placement, an open lysis of adhesions for small bowel obstruction (SBO), a laparoscopic lysis of adhesions for SBO, an open cholecystectomy, a laparoscopic cholecystectomy, and an excision of a round ligament endometrioma. There was only one death, which was in a patient with Type IV EDS who was the first patient in this series. He presented with a spontaneous sigmoid perforation treated by Hartmann procedure and went on to develop two more colon perforations and to die of sepsis. The morbidity included only two recurrent ventral hernias, a wound dehiscence, a wound hematoma, and recurrence of the anal fistula. Although patients with EDS pose significant healing problems, successful general surgical procedures can be performed in most patients. Among other recommendations, total avoidance of colon anastomoses and colostomies in favor of total abdominal colectomy and ileostomy and routine closure of the abdominal wall with mesh or retention sutures is advocated. Making the diagnosis is the key to having successful outcomes. Further recommendations on avoiding operation and on the conduct of the operation, if needed, are given.
埃勒斯-当洛综合征(EDS)是一组密切相关的疾病,由胶原蛋白合成的遗传性缺陷引起,这会导致明显的愈合困难。据估计,其发病率在2500分之一至5000分之一之间,但实际发生率可能比报告的更高。在普通外科医生的职业生涯中,可能都曾多次遇到过EDS患者。本报告的目的是描述那些应提高怀疑指数的发现,以协助诊断,并通过回顾一位外科医生管理此类患者的经验及相关文献,来描述EDS患者常见的普通外科手术情况。文中给出了治疗建议。本文报告了一位外科医生对15例EDS患者进行25例手术的回顾性经验。据信,这是迄今由一位外科医生报告的最大病例系列。所实施的手术种类繁多,包括腹疝修补术(n = 6)、腹股沟疝修补术(n = 4)、结肠切除术(n = 3)、肛瘘手术(n = 3),以及各1例的剖腹探查术、阑尾切除术、切口裂开缝合术、希克曼导管置入术、小肠梗阻粘连松解术(开放手术)、小肠梗阻粘连松解术(腹腔镜手术)、开腹胆囊切除术、腹腔镜胆囊切除术和圆韧带子宫内膜瘤切除术。仅1例死亡,该患者为IV型EDS,是本系列的首例患者。他因自发性乙状结肠穿孔接受哈特曼手术治疗,随后又出现两次结肠穿孔,最终死于败血症。并发症仅包括2例复发性腹疝、1例伤口裂开、1例伤口血肿和肛瘘复发。尽管EDS患者存在严重的愈合问题,但大多数患者仍可成功进行普通外科手术。除其他建议外,主张完全避免结肠吻合术和结肠造口术,而采用全腹结肠切除术和回肠造口术,并常规使用网片或保留缝线关闭腹壁。做出诊断是取得成功治疗效果的关键。文中还给出了关于避免手术以及必要时手术操作的进一步建议。