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动脉重建在自发性肾动脉夹层中的作用。

The role of arterial reconstruction in spontaneous renal artery dissection.

作者信息

Reilly L M, Cunningham C G, Maggisano R, Ehrenfeld W K, Stoney R J

机构信息

Department of Surgery, University of California, San Francisco 94143.

出版信息

J Vasc Surg. 1991 Oct;14(4):468-77; discussion 477-9.

PMID:1920644
Abstract

Spontaneous renal artery dissection is an uncommon cause of renovascular hypertension, usually associated with fibromuscular dysplasia. Among reported nonautopsy cases (N = 80), arterial reconstruction has seldom been attempted (N = 21) and the outcome has frequently been poor (48% clinical failure rate). This is attributed in part to the frequent involvement of renal artery branches by the dissection. Furthermore, the report of spontaneous reversion to normotension among patients treated medically has also clouded the role of surgery in this disease. Since progress in the technique of renal artery repair now allows successful treatment of anatomically complex lesions, we reviewed our experience with arterial reconstruction in the management of spontaneous renal artery dissection to determine the frequency of and factors correlating with cure after operative repair. Ten patients (eight men, two women; mean age, 39.3 +/- 5.9 years) were admitted with severe hypertension (10/10), often associated with neurologic symptoms, hematuria, or flank pain (8/10). Serum creatinine was elevated in only two patients. Angiography demonstrated changes consistent with fibromuscular dysplasia in 7 of 10 patients and evidence of dissection in 6 of 10. Bilateral disease was present in three patients. Only five patients had a single renal artery on the involved side. The dissection extended into the primary branches in 8 of 10 patients and involved both renal arteries in four of the five patients with two arteries. Histologic study confirmed fibromuscular dysplasia in six and intramural dissection in all operative specimens. Five patients underwent revascularization (in one case requiring the ex vivo technique), with use of hypogastric artery as a conduit in four of five or resection and primary reanastomosis in one of five. Three patients became normotensive, and two returned to their previous level of blood pressure control. Follow-up averaged 14.5 years. Two patients underwent nephrectomy after exploration demonstrated nonreconstructible vessels, and two underwent nephrectomy when intraoperative assessment of the kidney showed that revascularization had failed to adequately reverse extensive renal ischemia. After a mean follow-up of 14.6 years these patients remain normotensive, although two require antihypertensive medications. One patient was treated medically and is currently hypertensive off all medications. Nine of 10 patients have maintained a normal serum creatinine during follow-up. We conclude that renal revascularization is frequently successful in spontaneous renal artery dissection (five of seven, 71.4%) and results in sustained relief of hypertension with maximal conservation of renal tissue. This is important because of the young age at onset and the not infrequent occurrence of bilateral fibromuscular dysplasia, and even of dissection.(ABSTRACT TRUNCATED AT 400 WORDS)

摘要

自发性肾动脉夹层是肾血管性高血压的一种罕见病因,通常与纤维肌性发育异常相关。在已报道的非尸检病例(N = 80)中,很少尝试进行动脉重建(N = 21),且结果往往不佳(临床失败率为48%)。部分原因是夹层常累及肾动脉分支。此外,接受药物治疗的患者中出现血压自发恢复正常的报道也使手术在该病中的作用变得模糊。由于肾动脉修复技术的进步现在能够成功治疗解剖结构复杂的病变,我们回顾了我们在自发性肾动脉夹层治疗中进行动脉重建的经验,以确定手术修复后治愈的频率及相关因素。10例患者(8例男性,2例女性;平均年龄39.3±5.9岁)因严重高血压(10/10)入院,常伴有神经症状、血尿或胁腹痛(8/10)。仅2例患者血清肌酐升高。血管造影显示10例患者中有7例存在与纤维肌性发育异常一致的改变,10例中有6例有夹层证据。3例患者为双侧病变。受累侧仅5例患者有单一肾动脉。10例患者中有8例夹层延伸至主要分支,5例有两条肾动脉的患者中有4例双侧肾动脉均受累。组织学研究证实6例有纤维肌性发育异常,所有手术标本均有壁内夹层。5例患者接受了血管重建(1例需要体外技术),5例中有4例使用髂内动脉作为管道,5例中有1例进行了切除及一期再吻合。3例患者血压恢复正常,2例恢复到之前的血压控制水平。随访平均14.5年。2例患者在探查发现血管无法重建后接受了肾切除术,2例患者在术中评估肾脏显示血管重建未能充分逆转广泛的肾缺血时接受了肾切除术。平均随访14.6年后,这些患者血压仍正常,尽管2例需要抗高血压药物治疗。1例患者接受药物治疗,目前不服药时仍有高血压。10例患者中有9例在随访期间血清肌酐维持正常。我们得出结论,肾血管重建在自发性肾动脉夹层中常常成功(7例中的5例,71.4%),并能持续缓解高血压,最大程度地保留肾组织。这一点很重要,因为该病发病年龄较轻,双侧纤维肌性发育异常甚至夹层并不少见。(摘要截短至400字)

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