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慢性粒细胞白血病干扰素-α治疗期间发生的严重自身免疫性血小板减少性紫癜。

Severe autoimmune thrombocytopenic purpura during interferon-alpha therapy for chronic myelogenous leukemia.

作者信息

Arimura Kosei, Arima Naomichi, Ohtsubo Hideo, Matsushita Kakushi, Kukita Toshimasa, Ayukawa Tomoko, Kuroki Tomoaki, Tei Chuwa

机构信息

Department of Hematology and Immunology, Kagoshima University Hospital, Kagoshima, Japan.

出版信息

Acta Haematol. 2004;112(4):217-8. doi: 10.1159/000081276.

DOI:10.1159/000081276
PMID:15564735
Abstract

Interferon (IFN)-alpha is a leukocyte-derived cytokine and is used to treat several hematopoietic malignancies. The most common adverse effects of IFN-alpha are flu-like symptoms and usually insignificant. However, adverse effects due to autoimmune mechanisms are often hazardous and irreversible, although their frequency is low. In the present report, we describe a 55-year-old female with chronic myelogenous leukemia who developed severe autoimmune thrombocytopenia during IFN-alpha therapy. The lowest platelet count was 6 x 10(9)/l with severe hemorrhagic tendency. The present report strongly suggests the clinical importance of autoimmune thrombocytopenia as an adverse effect of IFN-alpha.

摘要

干扰素(IFN)-α是一种源自白细胞的细胞因子,用于治疗多种血液系统恶性肿瘤。IFN-α最常见的不良反应是类流感症状,通常不严重。然而,尽管自身免疫机制导致的不良反应发生率较低,但往往具有危险性且不可逆转。在本报告中,我们描述了一名55岁的慢性粒细胞白血病女性患者,她在接受IFN-α治疗期间发生了严重的自身免疫性血小板减少症。最低血小板计数为6×10⁹/L,伴有严重的出血倾向。本报告强烈提示自身免疫性血小板减少症作为IFN-α不良反应的临床重要性。

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