Yılmaz İnsu, Kaynar Leylagül, Tutar Nuri, Pala Çiğdem, Canöz Özlem, Yıldırım Afra, Büyükoğlan Hakan, Gülmez İnci
Department of Chest Diseases, Division of Immunology and Allergy, Erciyes University Faculty of Medicine, Kayseri, Turkey.
Department of Internal Medicine, Division of Hematology, Erciyes University Faculty of Medicine, Kayseri, Turkey.
Turk Thorac J. 2016 Jul;17(3):118-121. doi: 10.5578/ttj.30508. Epub 2016 Jul 1.
Hypereosinophilic syndomes (HESs) include potentially lethal multisystem disorders characterized by eosinophilic infiltration of a variable spectrum of target organs, predominantly the skin, heart, lungs, gastrointestinal tract, and nervous system. Based on recent advances in molecular and genetic diagnostic techniques and increasing experience with differences in clinical features and prognosis, subtypes have been defined, including "myeloproliferative-HES ", "lymphocytic-HES", "familial eosinophilia", "overlap HES", "undefined HES" ("complex undefined HES", "simple undefined HES", "episodic undefined HES") and "eosinophil associated diseases" (such as Churg-Strauss syndrome). HES should be kept in mind in the differential diagnosis of eosinophilic lung diseases especially in patients with peripheral eosinophilia and pulmonary infiltrates. Corticosteroids represent an effective firstline approach to decreasing eosinophil counts in the majority of cases. Imatinib might be used for corticosteroid nonresponders. We herein report a patient with "complex undefined HES" who had disease resistant to corticosteroids, but who had a significant response after treatment with imatinib.
高嗜酸性粒细胞综合征(HESs)包括潜在致命的多系统疾病,其特征为嗜酸性粒细胞浸润多种不同的靶器官,主要是皮肤、心脏、肺、胃肠道和神经系统。基于分子和基因诊断技术的最新进展以及对临床特征和预后差异的经验积累,已定义了多种亚型,包括“骨髓增殖性HES”、“淋巴细胞性HES”、“家族性嗜酸性粒细胞增多症”、“重叠性HES”、“未定型HES”(“复杂未定型HES”、“单纯未定型HES”、“发作性未定型HES”)以及“嗜酸性粒细胞相关疾病”(如Churg-Strauss综合征)。在嗜酸性粒细胞性肺病的鉴别诊断中应考虑到HES,尤其是在外周血嗜酸性粒细胞增多和肺部浸润的患者中。在大多数情况下,糖皮质激素是降低嗜酸性粒细胞计数的有效一线治疗方法。伊马替尼可用于对糖皮质激素无反应的患者。我们在此报告一例“复杂未定型HES”患者,该患者对糖皮质激素耐药,但在接受伊马替尼治疗后有显著反应。