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高嗜酸粒细胞综合征(hypereosinophilic syn-drome,HES)是临床上少见的血液系统疾病,该病多见于男性,好发于20～50岁,临床表现复杂,其症状和体征缺乏特异性,极易被误诊。2001年WHO发布的造血系统髓系肿瘤分类中将其和慢性嗜酸粒细胞白血病(CEL/HES)归类在慢性骨髓增殖性疾病(CMPD)之中,解决了其归类问题。随
Hypereosinophilic syn-drome (HES) is a clinically rare hematological disease. The disease is more common in men and occurs in patients aged 20 to 50 years. The clinical manifestations are complex and the symptoms and signs are not specific. Easily misdiagnosed. The WHO classification of myeloid tumors in the hematopoietic system released in 2001 by the WHO classifies chronic myelogenous leukemia (CEL / HES) in chronic myeloproliferative disorders (CMPD) and addresses its categorization. With