儿童特发性获得性再生障碍性贫血的远期预后及残留异常。

I Tsukimoto, M Tsuchida, A Ohara, T Akabane, T Nakahata, J Akatsuka, N Taguchi, T Nagao, G Tsujino, S Konishi
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引用次数: 0

摘要

评价儿童特发性获得性再生障碍性贫血的远期预后和治疗质量。在1965- 1985年登记的244例患者中,1965-1975年和1976-1985年登记的患者生存率分别为50.1%和62.0%。治愈率、治疗不足率和死亡率分别为30%、30%和40%。约40%的中度病例患者死亡或需要频繁输血。在小儿患者中,骨髓移植成功率高。对于诊断后3个月需要输血且有HLA相同供者的中度重症患者,应考虑采用这种方式。体格发育基本正常,但35%的患者在治疗过程中出现出血倾向、肝功能紊乱等残留异常。三分之一的患者出现血小板减少和造血功能低下,所有患者的干细胞检测结果均异常。50%的患者CD /8比值降低,15%的患者表现出心理问题。这些残留的异常会持续数年,有时会持续一生。
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Long-term prognosis and residual abnormalities of idiopathic acquired aplastic anemia in children.

We evaluated the long-term prognosis and quality of cure of idiopathic acquired aplastic anemia in children. Of the 244 patients registered from 1965 to 1985, those registered in 1965-1975 and 1976-1985 had a survival rate of 50.1% and 62.0%. The percentage of cure, undertreatment and death was 30, 30 and 40%, respectively. About 40% of the patients with moderate cases, died dead or required frequent blood transfusions. In the case of pediatric patients, as the success rate of bone marrow transplantation was high. This modality should be considered for patients with moderate severity who require blood transfusion 3 months after the diagnosis and an HLA identical donor is available. Physical development was almost normal but 35% of the patients showed residual abnormalities such as bleeding tendency, and hepatic disorders due to treatment. Thrombocytopenia and ineffective hematopoiesis were observed in one-third of the patients and all of the patients showed abnormal committed stem cell assay. The CD 4/8 ratio was reduced in 50% of the patients and 15% exhibited psychological problems. These residual abnormalities last for years, and sometimes a lifetime.

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The hematopoietic system [Application of nucleolar organizer region staining technique to air-dried blood smears]. [Biochemical and molecular biological studies on beta-glucuronidase in myelogenous leukemic cells]. [Production and secretion of BSF2/IL6 in a case of hairy cell leukemia with polyclonal hypergammaglobulinemia]. [Long-term cultures of marrow cells from the patients with aplastic anemia].
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