原发性嗜酸性粒细胞增多症罕见病例

A. Bs, Farzana Hoque
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引用次数: 0

摘要

嗜酸性粒细胞过多症是一种罕见的综合征,其病因多种多样,可偶发或在某些情况下危及生命。这是一个独特的病例,患者是一名 38 岁的男性,在一次脑血管事件后出现急性脑病,随后被发现嗜酸性粒细胞计数升高。当患者出现无明确病因的多器官功能障碍时,临床高度怀疑诊断这种罕见疾病至关重要,尤其是涉及相对年轻的患者急性发病时。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Rare Case of Primary Hypereosinophilic Syndrome
Hypereosinophilia is a rare collection of syndromes of various etiologies that can present incidentally or in some cases, in a life-threatening manner. This is a unique case of a 38-year-old male who presented with acute encephalopathy following a cerebrovascular event and was later found to have elevated eosinophil counts. It is crucial to have high clinical suspicion to diagnose this rare disease when a patient presents with multi-organ dysfunction with no clear etiology, especially when involving a presentation of acute onset in a relatively young patient. J MEDICINE 2024; 25: 94-97
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