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[锁骨下动脉动脉瘤]

[Aneurysms of the subclavian artery].

作者信息

Davidović L B, Lotina S I, Jakovljević N S, Pavlović G S, Kecman Lj

机构信息

Institute of Cardiovascular Diseases, Clinical Centre of Serbia, Belgrade.

出版信息

Srp Arh Celok Lek. 2000 May-Jun;128(5-6):184-90.

Abstract

INTRODUCTION

The Subclavian artery aneurysms are not a commonly seen peripheral aneurysm [1-5]-. We present the experience of the Institute of Cardiovascular Diseases of the Serbian Clinical Centre, Belgrade.

PATIENTS AND METHODS

Eight cases of subclavian artery aneurysms are presented. There were 3 male and 5 female patients, average age 51 (32-65) years. Of them 3 aneurysms were of atherosclerotic origin, 4 developed due to thoracic outlet syndrome (TOS), and one developed after intra-arterial drug injection. More details about our cases are presented in Table 1. One of our patients had intra-thoracal aneurysm (Case 3), and 7 had extra-thoracal aneurysm (Figure 1). Two aneurysms appeared as an asymptomatic pulsatile mass in supraclavicular space, and two with compression in the brachial plexus (Figure 2). Our patient 3 manifested skin necrosis and haemorrhage in supraclavicular region (Figure 3). The other 3 patients manifested acute hand ischaemia due to partial aneurysmal thrombosis and distal embolization. In these patients all distal arterial pulses were absent (Figures 4 and 5). In patient 8, besides hand ischaemia, transitory ischaemic attack (TIA) with contralateral hemiparesis also occurred. The reason was microembolization of ipsilateral carotid artery due to retrograde thrombo propagation. The diagnosis was established by selective angiography of the subclavian artery, and in 4 patients Duplex ultrasonography was also used. All patients were treated surgically. In 7 patients supraclavicular approach to subclavian artery was used, and in case 3 we used a combined trans-sternal and supraclavicular approach. In 7 patients a complete aneurysmal resection was performed, and in patient 5 due to infection aneurysm was excluded by proximal and distal arterial ligations. In this case arterial flow was reestablished by extra-atomic carotid axillary bypass with saphenous vein graft. In three patients with TOS, after aneurysmal resections, end-to-end anastomosis was performed. In patient 2 in whom aneurysm was also caused by TOS, saphenous vein graft was used for reconstruction. In all 4 patients with TOS, some kind of decompressive procedure at the thoracic outlet was also performed (two cervical and two first-rib resections using supraclavicular approach). In 3 patients with atherosclerotic subclavian artery aneurysms, PTFE graft was used for reconstruction (Figures 6 and 7).

RESULTS

One early postoperative complication occurred. It was embolism of the brachial artery which has been successfully treated by transbrachial embolectomy. The early patency rate was 88%. The patients were controlled using physical and Doppler ultrasonographic examinations 1, 3, 6, 12 months, and then every year postoperatively. The mean follow-up period was 3.6 (1-8) years. In that period one (13%) late complication was observed. It was thrombosis of the saphenous vein graft true aneurysm in our patient 2. This aneurysm was resected and replaced with PTFE graft. Postoperative histological examination showed connective tissue disorder of the vein wall. The long-term patency rate was 88%.

DISCUSSION

In most cases the true subclavian artery aneurysms are of atherosclerotic origin [1-4, 6, 7, 12]. We had 3 such cases. TOS is also often caused by subclavian artery true aneurysms [5, 13-17]. We had 4 such cases. Fibromuscular dysplasia [1, 18], cystic idiopathic medionecrosis [1, 19, 20], infection [1, 21, 22] and congenital disorders [23, 24], are rare causes of subclavian artery true aneurysms. Subclavian artery pseudoaneurysms can develop after different reconstructive vascular procedures [5, 28-41]. Subclavian artery aneurysms can rupture, thrombosis, embolize, or cause symptoms by local compression [6, 12, 41]. We had two cases with compression on brachial plexus. The compression on the trachea, oesophagus, laryngeal nerve, ganglion stellatum were also described [6, 12, 25, 42, 43]. Most subclavian artery aneurysms present ischaemic symptoms of

摘要

引言

锁骨下动脉瘤并非常见的周围动脉瘤[1 - 5]。我们介绍了贝尔格莱德塞尔维亚临床中心心血管疾病研究所的经验。

患者与方法

本文呈现了8例锁骨下动脉瘤病例。其中男性3例,女性5例,平均年龄51(32 - 65)岁。其中3例动脉瘤源于动脉粥样硬化,4例因胸廓出口综合征(TOS)形成,1例在动脉内药物注射后出现。表1展示了我们病例的更多详细信息。我们的1例患者患有胸内动脉瘤(病例3),7例为胸外动脉瘤(图1)。2例动脉瘤表现为锁骨上区域无症状性搏动性肿块,2例伴有臂丛神经受压(图2)。我们的患者3出现锁骨上区域皮肤坏死和出血(图3)。另外3例患者因部分动脉瘤血栓形成和远端栓塞表现为急性手部缺血。这些患者所有远端动脉搏动消失(图4和图5)。在患者8中,除了手部缺血,还发生了伴有对侧偏瘫的短暂性脑缺血发作(TIA)。原因是同侧颈动脉因逆行血栓传播发生微栓塞。通过锁骨下动脉选择性血管造影确诊,4例患者还使用了双功超声检查。所有患者均接受手术治疗。7例患者采用锁骨上入路处理锁骨下动脉,病例3采用经胸骨和锁骨上联合入路。7例患者进行了完整的动脉瘤切除术,患者5因感染通过近端和远端动脉结扎排除动脉瘤。在此病例中,通过大隐静脉移植的体外颈动脉腋动脉旁路重建动脉血流。3例TOS患者在动脉瘤切除术后进行了端端吻合。患者2的动脉瘤也由TOS引起,使用大隐静脉移植进行重建。所有4例TOS患者在胸廓出口处也进行了某种减压手术(2例采用锁骨上入路行颈椎和第1肋切除术)。3例动脉粥样硬化性锁骨下动脉瘤患者使用聚四氟乙烯(PTFE)移植物进行重建(图6和图7)。

结果

发生1例早期术后并发症。为肱动脉栓塞,通过经肱动脉取栓术成功治疗。早期通畅率为88%。术后1、3、6、12个月以及之后每年通过体格检查和多普勒超声检查对患者进行随访。平均随访期为3.6(1 - 8)年。在此期间观察到1例(13%)晚期并发症。为患者2的大隐静脉移植真性动脉瘤血栓形成。该动脉瘤被切除并用PTFE移植物替换。术后组织学检查显示静脉壁结缔组织紊乱。长期通畅率为88%。

讨论

在大多数情况下,真性锁骨下动脉瘤源于动脉粥样硬化[1 - 4, 6, 7, 12]。我们有3例此类病例。TOS也常由锁骨下动脉真性动脉瘤引起[5, 13 - 17]。我们有4例此类病例。纤维肌发育不良[1, 18]、囊性特发性中层坏死[1, 19, 20]、感染[1, 21, 22]和先天性疾病[23, 24]是真性锁骨下动脉瘤的罕见病因。锁骨下动脉假性动脉瘤可在不同的血管重建手术后形成[5, 28 - 41]。锁骨下动脉瘤可破裂、血栓形成、栓塞或通过局部压迫引起症状[6, 12, 41]。我们有2例臂丛神经受压病例。也有关于气管、食管、喉返神经、星状神经节受压的描述[6, 12, 25, 42, 43]。大多数锁骨下动脉瘤表现为缺血症状

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