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α干扰素治疗儿童原发性血小板增多症获持久部分缓解

Long-lasting partial remission by Interferon-alpha treatment in a child with essential thrombocythemia.

作者信息

Szegedi István, Benko Ilona, Mero Gabriella, Prinzinger Agota, Kappelmayer János, Kiss Csongor

机构信息

Department of Pediatrics, Medical and Health Science Center, University of Debrecen, Debrecen, Hungary.

出版信息

Pediatr Blood Cancer. 2007 Oct 15;49(5):744-7. doi: 10.1002/pbc.20744.

Abstract

Essential thrombocythemia (ET) is a clonal myeloproliferative disorder characterized by sustained thrombocytosis, isolated hyperplasia of megakaryocytic lineage, and association with thrombotic or bleeding episodes. It is extremely rare in childhood and frequently presents without evident clinical signs. We describe a 3-year-old girl with severe headache and dizziness suffering from ET, who was treated with Interferon-alpha-2a (IFN) based on the potent effect of this agent to inhibit myeloid colonies induced by phytohemagglutinin A stimulated leukocyte conditioned medium (PHA-LCM). Bone-marrow-derived mononuclear cells of this patient did not exhibit spontaneous colony formation but responded to recombinant human (rh) erythropoietin (EPO), rh granulocyte-colony stimulating factor (G-CSF), granulocyte-macrophage (GM)-CSF, and stem-cell factor in addition to PHA-LCM. After 65 months of in vivo IFN treatment, the patient experienced a sustained partial remission with platelet counts varying between 400 and 600 x 10(3)/microl.

摘要

原发性血小板增多症(ET)是一种克隆性骨髓增殖性疾病,其特征为持续性血小板增多、巨核细胞系孤立性增生,以及与血栓形成或出血事件相关。它在儿童期极为罕见,且常常在没有明显临床体征的情况下出现。我们描述了一名患有ET的3岁女童,她出现严重头痛和头晕症状,基于干扰素α-2a(IFN)对抑制由植物血凝素A刺激的白细胞条件培养基(PHA-LCM)诱导的髓系集落具有显著效果,对其进行了治疗。该患者的骨髓来源单核细胞未表现出自发集落形成,但除了对PHA-LCM有反应外,还对重组人(rh)促红细胞生成素(EPO)、rh粒细胞集落刺激因子(G-CSF)、粒细胞-巨噬细胞(GM)-CSF和干细胞因子有反应。经过65个月的体内IFN治疗,患者实现了持续部分缓解,血小板计数在400至600×10³/微升之间波动。

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