Anti-neutrophil Cytoplasmic Antibody-Associated Vasculitis Complicated by Subarachnoid Hemorrhage due to a Ruptured Cerebral Aneurysm: A Case Report.

NMC case report journal Pub Date : 2026-05-19 eCollection Date: 2026-01-01 DOI:10.2176/jns-nmc.2025-0378
Megumi Tomita, Junya Kaneko, Shodai Yamada, Shin Sato, Akiko Kitahashi, Tomohiro Kaneko, Masamune Kuno, Shoji Yokobori
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Abstract

Anti-neutrophil cytoplasmic antibody-associated vasculitis is an autoimmune disorder characterized by inflammation of small vessels, with potential for multi-organ involvement. Anti-neutrophil cytoplasmic antibody-associated vasculitis can affect blood vessels throughout the body, but involvement of cerebral vessels is relatively rare. We report a case of anti-neutrophil cytoplasmic antibody-associated vasculitis complicated by a subarachnoid hemorrhage due to the rupture of a cerebral artery pseudoaneurysm, which was successfully managed with endovascular intervention. A 61-year-old man presented with headache, purpura on the extremities, profound fatigue, and diffuse myalgia. Computed tomography revealed subarachnoid hemorrhage. Based on clinical, laboratory, brain magnetic resonance imaging, and cerebral angiography findings, the patient was diagnosed with anti-neutrophil cytoplasmic antibody-associated vasculitis and subarachnoid hemorrhage secondary to the rupture of pseudoaneurysm formed in perforating branch arising from the vertebral artery. Parent artery occlusion of the vertebral artery resulted in the complete obliteration of the aneurysm and no rebleeding occurred during the course. Despite intensive care management, the patient developed renal and putaminal hemorrhages, resulting in a fatal outcome. Anti-neutrophil cytoplasmic antibody-associated vasculitis may involve the cerebral vessels, and in cases complicated by ruptured aneurysms, implementing appropriate re-rupture prevention alongside adequate treatment of anti-neutrophil cytoplasmic antibody-associated vasculitis may help improve clinical outcomes.

脑动脉瘤破裂致抗中性粒细胞细胞质抗体相关血管炎并发蛛网膜下腔出血1例。
抗中性粒细胞细胞质抗体相关血管炎是一种以小血管炎症为特征的自身免疫性疾病,有可能累及多器官。抗中性粒细胞细胞质抗体相关的血管炎可累及全身血管,但累及脑血管是相对罕见的。我们报告一例抗中性粒细胞细胞质抗体相关的血管炎并发蛛网膜下腔出血,这是由于脑动脉假性动脉瘤破裂,这是成功地管理与血管内介入。男性,61岁,头痛,四肢紫癜,极度疲劳,弥漫性肌痛。计算机断层扫描显示蛛网膜下腔出血。根据临床、实验室、脑磁共振成像和脑血管造影结果,诊断为抗中性粒细胞细胞质抗体相关血管炎和蛛网膜下腔出血,继发于椎动脉穿支形成的假性动脉瘤破裂。母动脉闭塞椎动脉导致动脉瘤完全闭塞,过程中无再出血发生。尽管进行了重症监护,患者还是出现了肾脏和皮膜出血,导致了致命的结果。抗中性粒细胞细胞质抗体相关的血管炎可能累及脑血管,在并发动脉瘤破裂的病例中,实施适当的再破裂预防和抗中性粒细胞细胞质抗体相关血管炎的适当治疗可能有助于改善临床结果。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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