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以急性多发性脑梗死为表现的抗中性粒细胞胞浆抗体阴性的变应性肉芽肿性血管炎:一例报告

ANCA-Negative Churg-Strauss Syndrome Presenting as Acute Multiple Cerebral Infarcts: A Case Report.

作者信息

Psychogios Klearchos, Evmorfiadis Ilias, Dragomanovits Spyros, Stavridis Athanasios, Takis Konstantinos, Kaklamanis Loukas, Stathis Pantelis

机构信息

Stroke Unit, Mediterraneo Hospital, Athens, Greece.

Department of Thrombosis and Hemostasis, Mediterraneo Hospital, Athens, Greece.

出版信息

J Stroke Cerebrovasc Dis. 2017 Mar;26(3):e47-e49. doi: 10.1016/j.jstrokecerebrovasdis.2016.12.009. Epub 2017 Jan 5.

Abstract

Eosinophilic granulomatosis with polyangiitis (EGPA, previously named Churg-Strauss syndrome) is a form of necrotizing vasculitis occurring in patients with asthma and eosinophilia. Ischemic stroke is a relatively rare complication of the disease. We report a case of a 63-year-old woman with multiple embolic infarcts, hypereosinophilia (for >7 years), and skin rash. Elevated cardiac enzymes and cardiac magnetic resonance imaging were consistent with endomyocarditis. The simultaneous presence of history of asthma, sinusitis, hypereosinophilia, and vasculitis led to the diagnosis of EGPA. This case contributes to the recent debate of the 2 possible presentations of the disease according to the ANCA (antineutrophil cytoplasmic antibodies) status. We furthermore underscore the need for careful differential diagnosis of the "ANCA negative" cases with persistent hypereosinophilia from the idiopathic hypereosinophilic syndrome.

摘要

嗜酸性肉芽肿性多血管炎(EGPA,既往称为变应性肉芽肿性血管炎)是一种发生于哮喘和嗜酸性粒细胞增多患者的坏死性血管炎。缺血性脑卒中是该疾病相对罕见的并发症。我们报告一例63岁女性患者,有多发栓塞性梗死、嗜酸性粒细胞增多(超过7年)及皮疹。心肌酶升高和心脏磁共振成像符合心内膜炎表现。哮喘、鼻窦炎、嗜酸性粒细胞增多及血管炎病史同时存在,从而诊断为EGPA。该病例参与了近期关于该疾病根据抗中性粒细胞胞浆抗体(ANCA)状态的两种可能表现形式的讨论。我们还强调了对于持续嗜酸性粒细胞增多的“ANCA阴性”病例与特发性嗜酸性粒细胞增多综合征进行仔细鉴别诊断的必要性。

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