Raman J, Saldanha R F, Esmore D S, Spratt P M, Farnsworth A E, Chang V P, Shanahan M X
Cardiothoracic Surgical Unit, St. Vincent's Hospital, Sydney, Australia.
J Cardiovasc Surg (Torino). 1988 Nov-Dec;29(6):647-9.
The Ehlers-Danlos syndrome (EDs) is one of the most frequently encountered inherited disorders of connective tissue. The arterial-ecchymotic type IV is notorious for large vessel involvement associated with spontaneous catastrophic bleeding. Most of these patients who require cardiovascular surgical procedures have a poor prognosis. Our experience of two patients, with aneurysmal dilatation of the ascending aorta is presented. The first patient presented with an aortic dissection extending from the ascending aorta to the common iliac arteries. The second patient presented with asymptomatic but progressive aneurysmal dilatation of the aortic root. Both patients underwent the Bentall procedure using a 25 mm St. Jude composite valved conduit. Despite increased vascular friability, both of these patients tolerated the operative procedure without complication and are doing well on early follow-up. This experience suggests that the Bentall procedure may be used to decrease the risks of dissection and rupture of the ascending aorta in patients with Ehlers-Danlos syndrome.
埃勒斯-当洛综合征(EDS)是最常见的遗传性结缔组织疾病之一。动脉瘀斑型IV型以累及大血管并伴有自发性灾难性出血而臭名昭著。大多数需要进行心血管外科手术的此类患者预后较差。本文介绍了我们对两名升主动脉瘤样扩张患者的治疗经验。首例患者表现为主动脉夹层,从升主动脉延伸至双侧髂总动脉。第二例患者表现为主动脉根部无症状但进行性的瘤样扩张。两名患者均使用25mm圣犹达复合带瓣管道进行了Bentall手术。尽管血管脆性增加,但这两名患者均耐受手术且无并发症,早期随访情况良好。这一经验表明,Bentall手术可用于降低埃勒斯-当洛综合征患者升主动脉夹层和破裂的风险。