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首页> 外文期刊>Case Reports in Otolaryngology >A Very Rare Case of Hypereosinophilic Syndrome Secondary to Natural Killer/T-Cell Lymphoma
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A Very Rare Case of Hypereosinophilic Syndrome Secondary to Natural Killer/T-Cell Lymphoma

机译：自然杀手/ T细胞淋巴瘤继发的罕见的嗜酸性粒细胞增多综合征

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Hypereosinophilic syndrome (HES) is a systemic disease characterized by an increased peripheral blood eosinophil count accompanied by systemic organ dysfunction. HES is classified into idiopathic HES, primary (neoplastic) HES (HESN), and secondary (reactive) HES (HESR). In this case report, a patient who developed peripheral blood eosinophilia and granulation tissue in the pharynx and paranasal sinus, which was initially diagnosed as chronic eosinophilic leukemia (CEL), categorized as HESN, but was eventually identified after the patient had died as natural killer/T-cell (NK/T) lymphoma, nasal type (ENKL), categorized as HESR, is presented. ENKL-induced HES is very rare but must be considered.
机译：高嗜酸性粒细胞综合征（HES）是一种全身性疾病，其特征在于外周血嗜酸性粒细胞计数增加，并伴有全身器官功能障碍。 HES分为特发性HES，原发性（肿瘤性）HES（HESN）和继发性（反应性）HES（HESR）。在该病例报告中，一名患者的咽部和副鼻窦出现外周血嗜酸性粒细胞增多和肉芽组织，最初被诊断为慢性嗜酸性粒细胞白血病（CEL），被归类为HESN，但在该患者死亡后被鉴定为自然杀手介绍了归类为HESR的鼻型/ T细胞（NK / T）淋巴瘤（ENKL）。 ENKL诱导的HES非常罕见，但必须考虑。

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