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自身免疫性疾病患者孤立性胸段脊髓前动脉动脉瘤:一例报告

Isolated Thoracic Anterior Spinal Artery Aneurysm in a Patient With Autoimmune Disease: A Case Report.

作者信息

Ahmadpour Arjang, Morsi Rami Z, Al-Salihi Mohammed Maan, Kass-Hout Tareq

机构信息

Department of Neurosurgery, University of Chicago, Chicago, USA.

Department of Neurology, University of Chicago, Chicago, USA.

出版信息

Cureus. 2024 Jul 19;16(7):e64943. doi: 10.7759/cureus.64943. eCollection 2024 Jul.

Abstract

This case report describes a rare presentation of a mycotic anterior spinal artery aneurysm of the thoracic spine presenting as a subarachnoid hemorrhage. Isolated anterior spinal artery aneurysms are exceedingly rare. While this condition can occur in the setting of an underlying infection that may lead to shock, other signs and symptoms of the infection itself typically manifest before the development of the aneurysm and subsequent hemorrhage. We present a case of a 30-year-old male who presented with acute-onset bilateral lower extremity motor paraplegia and was found to have diffuse subarachnoid hemorrhage related to an isolated thoracic anterior spinal artery aneurysm, which was believed to be mycotic in origin. Spinal angiogram revealed evidence of an aneurysm originating from the anterior spinal artery at the T11-T12 level, contributing to diffuse subarachnoid hemorrhage of the spinal cord. The patient was followed closely and exhibited progressive improvement in motor function. Magnetic resonance imaging performed two weeks later revealed decreased intrathecal hemorrhage, mild spinal cord edema, and a reduction in the discrete visualization of the anterior spinal artery aneurysm. We present a unique case of an isolated anterior spinal artery aneurysm in the thoracic spine presenting with subarachnoid hemorrhage. This case is distinctive in that the clinical presentation and radiographic findings strongly suggest a mycotic etiology for the aneurysm, despite the absence of definitive histopathologic confirmation. To our knowledge, this is the first reported case of an isolated thoracic ASA aneurysm suspected to be mycotic in origin.

摘要

本病例报告描述了一例罕见的胸椎霉菌性脊髓前动脉动脉瘤,表现为蛛网膜下腔出血。孤立性脊髓前动脉动脉瘤极为罕见。虽然这种情况可发生在潜在感染导致休克的情况下,但感染本身的其他体征和症状通常在动脉瘤形成及随后出血之前就已出现。我们报告一例30岁男性患者,其急性起病,出现双侧下肢运动性截瘫,经检查发现与一个孤立的胸段脊髓前动脉动脉瘤相关的弥漫性蛛网膜下腔出血,该动脉瘤被认为是霉菌性起源。脊髓血管造影显示在T11 - T12水平有一个起源于脊髓前动脉的动脉瘤,导致脊髓弥漫性蛛网膜下腔出血。对该患者进行密切随访,其运动功能逐渐改善。两周后进行的磁共振成像显示鞘内出血减少、脊髓轻度水肿,脊髓前动脉动脉瘤的清晰显影减少。我们报告了一例独特的胸段孤立性脊髓前动脉动脉瘤伴蛛网膜下腔出血的病例。该病例的独特之处在于,尽管缺乏明确的组织病理学证实,但临床表现和影像学检查结果强烈提示该动脉瘤为霉菌性病因。据我们所知,这是首例报告的疑似霉菌性起源的孤立性胸段脊髓前动脉动脉瘤病例。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/70df/11330671/ec06047da4b5/cureus-0016-00000064943-i01.jpg

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