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上肢纤维肌发育不良的临床表现、临床特征及干预结果

Presentation, clinical features, and results of intervention in upper extremity fibromuscular dysplasia.

作者信息

Nguyen Nancy, Sharma Aditya, West Jonathan K, Serhal Maya, Brinza Ellen, Gornik Heather L, Kim Esther S H

机构信息

Department of Cardiovascular Medicine, Cleveland Clinic, Cleveland, Ohio.

Department of Medicine, Cardiovascular Medicine Division, University of Virginia, Charlottesville, Va.

出版信息

J Vasc Surg. 2017 Aug;66(2):554-563. doi: 10.1016/j.jvs.2017.02.049.

DOI:10.1016/j.jvs.2017.02.049
PMID:28735951
Abstract

BACKGROUND

We present a case series of upper extremity fibromuscular dysplasia (UE FMD) consisting of 22 patients from two tertiary referral centers focusing on clinical presentation, diagnostic findings, and interventional outcomes. FMD is a noninflammatory, nonatherosclerotic arteriopathy that has a predisposition for middle-aged women. Involvement of the UE is thought to be rare. Patients with UE FMD can present with claudication or ischemia, or they can be incidentally diagnosed. The treatment approach is dictated by clinical presentation.

METHODS

Data were collected of patients with UE FMD evaluated at two centers. Demographic data, presenting UE symptoms, UE arteries involved, FMD type, diagnostic method, physical examination findings, management, and outcomes were included.

RESULTS

Twenty-two patients (29 limbs) were diagnosed with UE FMD. The brachial artery was most commonly involved (89.7% of affected limbs). More than half of limbs (n = 15 of 29 limbs [51.7%]) were asymptomatic, and of those who presented with symptoms, the most common symptoms were ischemic fingers or hand (31% of all affected limbs) and hand or arm claudication (27.6% of all affected limbs). UE FMD was noted on catheter angiography in 58.6% (n = 17 of 29 limbs), duplex ultrasound in 41.4% (n = 12 of 29 limbs), and computed tomography angiography in 27.6% (n = 8 of 29 limbs). Of the symptomatic limbs (n = 14), the majority were treated solely with medical therapy as the first intervention (57.1%). For symptomatic limbs treated with vascular intervention (n = 5), angioplasty was most commonly performed. Only 4 of the 14 limbs (28.6%) had complete symptomatic relief after the initial first intervention, in which 2 limbs were treated with medical therapy, 1 limb underwent angioplasty, and 1 limb had resolution of symptoms despite deferment of any therapy. Of the 10 limbs with residual symptoms after the first intervention, 6 limbs underwent a second intervention: angioplasty in 2 limbs initially treated medically (33.3%), surgical bypass in 2 limbs initially treated with angioplasty, surgical bypass in 1 limb initially treated with medical therapy, and sympathectomy in 1 limb (16.7%) initially treated with angioplasty. Both surgical bypass and angioplasty as secondary interventions resulted in complete symptom relief.

CONCLUSIONS

Presenting symptoms for patients with UE FMD vary in severity from asymptomatic disease to digital ischemia. More than half of symptomatic limbs eventually require at least one invasive intervention for complete relief of symptoms.

摘要

背景

我们报告了一组上肢纤维肌性发育异常(UE FMD)病例系列,共22例患者,来自两个三级转诊中心,重点关注临床表现、诊断结果和介入治疗效果。FMD是一种非炎性、非动脉粥样硬化性动脉病,好发于中年女性。上肢受累被认为较为罕见。UE FMD患者可表现为间歇性跛行或缺血,也可能是偶然诊断出来的。治疗方法取决于临床表现。

方法

收集在两个中心评估的UE FMD患者的数据。包括人口统计学数据、上肢出现的症状、受累的上肢动脉、FMD类型、诊断方法、体格检查结果、治疗及结果。

结果

22例患者(29条肢体)被诊断为UE FMD。肱动脉最常受累(占受累肢体的89.7%)。超过一半的肢体(29条肢体中的15条[51.7%])无症状,有症状的患者中,最常见的症状是手指或手部缺血(占所有受累肢体的31%)和手部或手臂间歇性跛行(占所有受累肢体的27.6%)。29条肢体中有58.6%(17条)在导管血管造影时发现UE FMD,41.4%(12条)在双功超声检查时发现,27.6%(8条)在计算机断层血管造影时发现。在有症状的肢体(14条)中,大多数作为首次干预仅接受药物治疗(57.1%)。对于接受血管介入治疗的有症状肢体(5条),最常进行的是血管成形术。14条肢体中只有4条(28.6%)在首次干预后症状完全缓解,其中2条肢体接受药物治疗,1条肢体接受血管成形术,1条肢体尽管未进行任何治疗但症状自行缓解。在首次干预后仍有残留症状的10条肢体中,6条肢体接受了二次干预:最初接受药物治疗的2条肢体进行了血管成形术(33.3%),最初接受血管成形术的2条肢体进行了外科搭桥手术,最初接受药物治疗的1条肢体进行了外科搭桥手术,最初接受血管成形术的1条肢体进行了交感神经切除术(16.7%)。外科搭桥手术和血管成形术作为二次干预均使症状完全缓解。

结论

UE FMD患者的症状严重程度不一,从无症状到手指缺血。超过一半有症状的肢体最终需要至少一次侵入性干预才能完全缓解症状。

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