[非霍奇金淋巴瘤男孩继发性骨髓增生异常综合征]。

Q4 Medicine
Cesko-Slovenska Pediatrie Pub Date : 1993-11-01
H Hrstková, V Cíhalová, M Pejchlová, M Vrba
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引用次数: 0

摘要

作者描述了一个男孩继发性骨髓增生异常综合征(MDS)发展成急性白血病的病例史。后者对治疗很有抵抗力。该疾病之前曾接受过高恶性程度的NH淋巴瘤放疗和化疗。作者给出了给病人的所有细胞抑制剂的总剂量。MDS诊断前一年的外周血细胞遗传学检查显示,从数量和结构方面高度病理核型。其中第1号染色体单体。5被发现,这是MDS的典型特征,这些变化通常表明预后较差,较早转化为急性白血病。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
[Secondary myelodysplastic syndrome in a boy with non-Hodgkin's lymphoma].

The authors describe the case-history of a boy with secondary myelodysplastic syndrome (MDS) which developed into acute leukaemia. The latter was quite resistant to treatment. The disease was preceded by treatment of NH lymphoma with a high grade of malignity by radiotherapy and chemotherapy. The authors give the total doses of all cytostatics which were administered to the patient. One year prior to diagnosis of MDS cytogenetic examination of peripheral blood revealed a highly pathological karyotype, from the numerical and structural aspect. Among others monosomy of chromosome no. 5 was found which is typical for MDS and these changes indicate as a rule a poor prognosis and relatively early transformation to acute leukaemia.

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来源期刊
Cesko-Slovenska Pediatrie
Cesko-Slovenska Pediatrie Medicine-Pediatrics, Perinatology and Child Health
CiteScore
0.30
自引率
0.00%
发文量
32
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