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特发性嗜酸粒细胞增多综合征(IHES)是指无明确致病因素、存在持续的嗜酸粒细胞(EC)血症(外周血EC绝对数大于1.5×109/L)并伴有器官损害的一种疾病~[1]。IHES多发于中年以上男性,儿童和青少年罕见,该疾病可累及各系统,心脏、皮肤和神经系统最常受累~[2]。该病属于罕见疾病,临床表现复杂多样且缺乏特异性,而临床上反应性或继发性EC增多的原因很多,故首诊常易误诊误治。现报道我
Idiopathic eosinophilia syndrome (IHES) refers to no specific risk factors, there is persistent eosinophilia (EC absolute number of peripheral blood greater than 1.5 × 109 / L) and accompanied by organs A disease that damages ~ [1]. IHES occurs frequently in middle-aged men, children and adolescents, which can affect the most commonly affected systems, heart, skin, and nervous system [2]. The disease is a rare disease, the clinical manifestations of complex and diverse and lack of specificity, and clinically reactive or secondary EC increased for many reasons, so the first diagnosis often misdiagnosis and misdiagnosis. Now report me