Subarachnoid Hemorrhage and Prostatic Involvement in Granulomatosis with Polyangiitis – An Atypical Presentation

R. Chu, P. Wong, J. K. M. Wai, F. Yap
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Abstract

Granulomatosis with Polyangiitis (GPA) is a form of Anti-neutrophil cytoplasmic antibody (ANCA)-associated vasculitis. We report a case of a 56-year-old man with GPA who first presented with acute urinary retention, and then developed pulmonarycavitating lesions and subarachnoid hemorrhage (SAH). The SAH was due to a ruptured right vertebral artery aneurysm, whichwas subsequently embolized. The patient initially had a good response to immunosuppressive therapy but later succumbed due to fulminant sepsis. SAH is a rare complication of GPA and usually not associated with a detectable aneurysm. Our patient is thesecond case in the literature where an aneurysm had been detected on angiography and the first case where examination of the culprit aneurysm revealed features of vasculitis.
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肉芽肿合并多血管炎时蛛网膜下腔出血及前列腺受累-一个不典型的表现
肉芽肿伴多血管炎(GPA)是一种抗中性粒细胞胞浆抗体(ANCA)相关血管炎。我们报告了一例56岁的GPA患者,他首先出现急性尿潴留,然后出现肺空洞病变和蛛网膜下腔出血(SAH)。SAH是由于右椎动脉瘤破裂,随后栓塞。患者最初对免疫抑制治疗反应良好,但后来因暴发性败血症而死亡。SAH是一种罕见的GPA并发症,通常与可检测的动脉瘤无关。我们的患者是文献中第二个在血管造影术中检测到动脉瘤的病例,也是第一个对罪魁祸首动脉瘤的检查显示血管炎特征的病例。
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审稿时长
12 weeks
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