Subclavian artery pseudoaneurysm

锁骨下动脉假性动脉瘤
  • 文章类型: Case Reports
    锁骨下和甲状腺颈干假性动脉瘤是罕见的病理,当它们同时发生时更是如此。这些血管损伤的治疗可以通过血管内或开放手术进行。我们提出了一个小说两阶段,混合开放和血管内的方法来管理一个健康的41岁的男性没有结缔组织疾病的个人或家族史,表现为锁骨下分支和甲状腺颈干假性动脉瘤并发肱动脉闭塞。假性动脉瘤采用微血管塞展开治疗,接着锁骨下动脉覆盖支架置入术,通过开放血栓切除术和补片血管成形术治疗肱动脉闭塞。患者康复,无任何并发症。
    Subclavian and thyrocervical trunk pseudoaneurysms are rare pathologies and even more so when they occur simultaneously. Treatment of these vascular injuries can be done endovascularly or with open surgery. We present a novel two-stage, hybrid open and endovascular approach to the management of a healthy 41-year-old man with no personal or family history of connective tissue disorders, who presented with subclavian branch and thyrocervical trunk pseudoaneurysms complicated by brachial artery occlusion. The pseudoaneurysms were treated with microvascular plug deployment, followed by subclavian artery covered stenting, with treatment of the brachial occlusion via open thrombectomy with patch angioplasty. The patient recovered without any complications.
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  • 文章类型: Case Reports
    锁骨下动脉假性动脉瘤(PSA)是高危经皮冠状动脉介入治疗(PCI)期间经腋窝Impella装置放置引起的罕见并发症。尽管Impella的使用越来越普遍,解决这一并发症的文献很少。该病例强调了锁骨下动脉PSA的现有证据有限,并强调了将其视为潜在风险的重要性。随着高风险PCI和Impella使用的普及,了解这种并发症对于早期发现和适当管理至关重要.一名62岁男性,既往有II型糖尿病病史,外周动脉疾病,高血压,慢性烟草使用表现为反复发作的劳力性胸痛和呼吸困难。最初的心电图检查显示前间隔导联ST段抬高。患者接受了左右两侧的心导管插入术,显示左前降支严重狭窄和心源性休克。在手术过程中,患者需要使用经皮左心室辅助装置进行机械循环支持;由于患者的双侧股动脉患有外周动脉疾病,因此通过经腋窝入路放置。病人有一个复杂的临床过程,但是病人的临床表现慢慢改善,移除经皮左心室辅助装置。移除装置大约六周后,患者在左肩前方的胸壁出现大量液体积聚。影像学显示左锁骨下动脉远端PSA破裂。患者被迅速带到导管插入实验室,并在PSA部位展开覆膜支架。重复血管造影显示,通过左锁骨下动脉进入腋窝动脉的血流很快,没有外渗到胸壁。
    Subclavian artery pseudoaneurysm (PSA) is a rare complication arising from transaxillary Impella device placement during high-risk percutaneous coronary intervention (PCI). Despite the increasing prevalence of Impella use, literature addressing this complication is scarce. This case emphasizes the limited existing evidence on subclavian artery PSA and highlights the importance of recognizing it as a potential risk. With high-risk PCI and Impella use gaining popularity, understanding this complication is crucial for early detection and appropriate management. A 62-year-old male with a past medical history of type II diabetes mellitus, peripheral artery disease, hypertension, and chronic tobacco use presents with recurrent episodes of exertional chest pain and dyspnea. Initial workup with an electrocardiogram showed ST-segment elevations in the anteroseptal leads. The patient underwent right- and left-sided cardiac catheterization, which revealed severe stenosis of the left anterior descending artery and findings of cardiogenic shock. The patient required mechanical circulatory support with a percutaneous left ventricular assist device during the procedure; this was placed via transaxillary approach due to the patient having peripheral artery disease in bilateral femoral arteries. The patient had a complicated clinical course, but the patient\'s clinical picture slowly improved, and the percutaneous left ventricular assist device was removed. Roughly six weeks after the removal of the device, the patient developed a large fluid collection in the chest wall anterior to the left shoulder. Imaging revealed a ruptured left distal subclavian artery PSA. The patient was promptly taken to the catheterization laboratory and a covered stent was deployed over the site of the PSA. Repeat angiography revealed brisk flow through the left subclavian artery into the axillary artery with no extravasation into the chest wall.
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  • 文章类型: Case Reports
    The vascular involvement in patients with Behcet\'s disease is defined as vascular Behcet\'s disease, which can greatly influence the prognosis. However, there are few reports on endovascular treatment (EVT) for subclavian pseudoaneurysms with long-term prognosis over 10 years. We present the case of a 42-year-old man with left subclavian artery pseudoaneurysm due to vascular Behcet\'s disease who was treated with EVT along with immunosuppressive therapies. Subsequently, 8 years after, the aneurysm recurred in the stent with stent fracture. Therefore, additional EVT was performed. We present the details of the patient\'s clinical course over 10 years after the EVT. .
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  • 文章类型: Case Reports
    We present a rare case of a 10-cm right subclavian artery pseudoaneurysm, with slow growth over 4 years after a traumatic fracture of the right clavicle. The patient had multiple prior endovascular attempts of embolization and stenting at other hospitals; despite this the pseudoaneurysm continued to grow and caused mass effect and neurologic symptoms. We present our open approach for the repair and a review of literature.
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  • 文章类型: Case Reports
    A young male patient presented at a tertiary care hospital with cold and bluish left upper limb accompanied with digital gangrene arousing suspicion of peripheral vascular disease. History did not reveal any high-risk behavior. Clinical examination and subsequent investigations lead to the diagnosis of acute infective endocarditis of native aortic valve along with peripheral embolism caused by methicillin-resistant Staphylococcus aureus. Fogarty\'s balloon embolectomy was done following which patient developed pseudoaneurysm of the left subclavian artery. These iatrogenic sequelae were managed with the resection of the pseudoaneurysm and prolonged antibiotic therapy as per the culture and sensitivity report.
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  • 文章类型: Case Reports
    Ultrasound-guided thrombin injection has been well described as a safe and effective treatment for pseudoaneurysms of the femoral artery. However, cases for subclavian artery pseudoaneurysm are rare. An 82-year-old man developed an iatrogenic right subclavian artery pseudoaneurysm. The pseudoaneurysm, which was partially thrombosed, was successfully treated by ultrasound-guided percutaneous thrombin injection. A trial injection with saline under color Doppler ultrasonography was helpful for confirming that the tip of the needle was in the sac with blood flow in the partially thrombosed pseudoaneurysm. Ultrasound-guided thrombin injection can be the first treatment of choice to treat subclavian artery pseudoaneurysm.
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  • 文章类型: Journal Article
    Behçet病(BD)是一种病因不明的罕见慢性系统性血管炎,常见于年轻人。我们报告了一个非常罕见的病例,该病例是一名70岁的男性,有40年的肠道BD病史,在左锁骨骨折后发现的左锁骨下动脉假性动脉瘤。患者在大约5个月前从床上摔下来后,通过绑扎固定治疗骨折,由于发现左锁骨下搏动性肿块,他被转诊到我们医院。增强计算机断层扫描显示左锁骨下动脉假性动脉瘤,它是使用血管内支架移植物修复的。
    Behçet\'s disease (BD) is a rare chronic systemic vasculitis of unknown etiology that presents in young adults. We report a very rare case of a left subclavian artery pseudoaneurysm identified after a left clavicle fracture in a 70-year-old man with a 40-year history of intestinal BD. The patient received fixation by banding to treat a fracture after falling from a bed about 5 months previously, and he was referred to our hospital due to the finding of a left subclavian pulsatile mass. As enhanced computed tomography showed a left subclavian artery pseudoaneurysm, it was repaired using an endovascular stent graft.
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  • 文章类型: Case Reports
    A rare case of a 56-year-old man with posttraumatic false aneurysm of the right subclavian artery is presented. He was admitted to hospital due to pain in the shoulder. The diagnosis was made upon ultrasonography and computed tomography (CT) results. With ultrasound guidance, the aneurysm was punctured and injected with bovine thrombin (Biotrombina 400u, Biomed). During the injection, the aneurysm neck was occluded by an endovascular balloon placed in the subclavian artery. Complete aneurysm embolisation was confirmed by ultrasound and CT studies. The postoperative course was complicated by Horner\'s syndrome which resolved completely within 3 weeks. The procedure technique is described in detail.
    W pracy przedstawiono rzadki przypadek 56-letniego mężczyzny z pourazowym rzekomym tętniakiem prawej tętnicy podobojczykowej. Chory został przyjęty do szpitala z powodu bólu barku, a rozpoznanie ustalono na podstawie badania ultrasonograficznego (USG) i angiografii tomografii komputerowej. Wykonano embolizację tętniaka za pomocą trombiny bydlęcej podanej pod kontrolą USG. Podczas iniekcji szyję tętniaka zabezpieczono balonem wewnątrznaczyniowym rozprężonym w tętnicy podobojczykowej prawej. Skuteczność embolizacji potwierdzono badaniem angiografii tomografii komputerowej. Przebieg pooperacyjny był powikłany wystąpieniem zespołu Hornera, który ustąpił po 3 tygodniach. W pracy dokładnie przedstawiono technikę postępowania chirurgicznego.
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