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环孢素用于嗜酸性粒细胞增多综合征。

Cyclosporin for hypereosinophilic syndrome.

作者信息

Zabel P, Schlaak M

机构信息

Medizinische Klinik, Forschungsinstitut Borstel, FRG.

出版信息

Ann Hematol. 1991 Jun;62(6):230-1. doi: 10.1007/BF01729838.

Abstract

The idiopathic hypereosinophilic syndrome (HES) comprises a heterogeneous group of disorders with unknown pathogenesis characterized by persistent peripheral blood and bone marrow eosinophilia and eosinophil infiltrates of multiple organs, leading to severe organ dysfunction. Lymphokine-mediated T-lymphocyte control of human eosinophilic granulopoiesis is though to play a major role in the pathogenesis of HES. Treatment of this disease with cyclosporin-A (CSA) therefore appears to be sensible. We report the case of a patient with a severe HES who failed to respond adequately to glucocorticoid treatment. With additional CSA therapy, disease activity showed a favorable remission and eosinophil counts rapidly decreased to the normal range and remained normal even after reduction of the methylprednisolone dosage to 7.5 mg daily. To date his remission has continued for more than 6 months. In the meantime we have confirmed the beneficial effects of CSA in two other cases of HES. This suggests that CSA treatment is justified, at least in combination with glucocorticoids, in severe cases of HES to prevent the side effects of a long-lasting high-dose glucocorticoid therapy.

摘要

特发性嗜酸性粒细胞增多综合征(HES)是一组发病机制不明的异质性疾病,其特征为外周血和骨髓嗜酸性粒细胞持续增多以及多个器官出现嗜酸性粒细胞浸润,进而导致严重的器官功能障碍。淋巴细胞介导的T淋巴细胞对人类嗜酸性粒细胞生成的控制被认为在HES的发病机制中起主要作用。因此,用环孢素A(CSA)治疗这种疾病似乎是合理的。我们报告了1例严重HES患者,该患者对糖皮质激素治疗反应不佳。加用CSA治疗后,疾病活动度出现良好缓解,嗜酸性粒细胞计数迅速降至正常范围,即使将甲泼尼龙剂量减至每日7.5mg后仍保持正常。迄今为止,他的缓解状态已持续超过6个月。同时,我们在另外2例HES患者中证实了CSA的有益作用。这表明,至少在重症HES病例中,为预防长期大剂量糖皮质激素治疗的副作用,CSA治疗(至少与糖皮质激素联合使用)是合理的。

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