Uppal Salil, Goel Sandeep, Randhawa Baljit, Maheshwary Ankush
Neurology, Uppal Neuro Hospital (UNH), Amritsar, IND.
Medicine, Government Medical College, Amritsar, IND.
Cureus. 2020 Sep 12;12(9):e10403. doi: 10.7759/cureus.10403.
Autoimmune-associated vasculitis is related to conditions like granulomatosis with polyangiitis (GPA) and eosinophilic polyangiitis with granulomatosis (EGPA), among many others. An unlikely scenario is patients with the above conditions presenting with ischemic strokes before any renal or pulmonary pathology. These conditions are associated with increased antineutrophillic cytoplasmic antibodies (C-ANCA) levels in the blood, and its decline after treatment is directly proportional to the recovery of the patient. We present a case of a previously healthy 38-year-old male patient who presented with acute/subacute ischemic stroke with elevated C-ANCA levels; his MRI brain images revealed multiple posterior circulation infarcts with hemorrhagic transformation. With pulse steroid therapy, he had significant improvement in neurological functions. This case report highlights the importance of maintaining a high degree of suspicion and providing early treatment for autoimmune strokes in young patients with no clear etiology for such a presentation.
自身免疫相关血管炎与多种疾病相关,如肉芽肿性多血管炎(GPA)和嗜酸性肉芽肿性多血管炎(EGPA)等。一种不太可能出现的情况是,患有上述疾病的患者在出现任何肾脏或肺部病变之前就发生缺血性中风。这些疾病与血液中抗中性粒细胞胞浆抗体(C-ANCA)水平升高有关,治疗后其水平下降与患者的恢复直接相关。我们报告一例38岁既往健康的男性患者,他因急性/亚急性缺血性中风就诊,C-ANCA水平升高;他的脑部MRI图像显示多个后循环梗死灶并伴有出血转化。经过脉冲类固醇治疗,他的神经功能有显著改善。本病例报告强调了对于无明确病因的年轻自身免疫性中风患者保持高度怀疑并提供早期治疗的重要性。