Pérez-Losada A, Woessner S, Solé F, Florensa L, Grañena A
Hospital Central L'Aliancça de Barcelona, Unitat d'Hematologia i Oncologia, España.
Acta Haematol. 1994;91(2):80-3. doi: 10.1159/000204259.
We report a case with refractory anaemia terminating in an acute leukaemia, which showed from the very beginning an intense eosinophilia that lasted for the whole disease, and in which the eosinophilic metaphases, as documented by the 'Morphology, Antibody, Chromosome' technique, were normal. An unusual karyotypic anomaly in the setting of a myelodysplastic syndrome could only be detected in the neutrophilic series. A general approach to detect structural aberrations of specific human chromosomes in metaphase cells by chromosomal in situ suppression hybridization of DNA libraries from sorted human chromosomes has been applied for chromosomes 11, 3 and 2, in order to identify an extra copy of chromosome 2.
我们报告了一例难治性贫血最终发展为急性白血病的病例,该病例从一开始就表现出强烈的嗜酸性粒细胞增多,且在整个病程中持续存在,并且通过“形态学、抗体、染色体”技术记录的嗜酸性中期相是正常的。骨髓增生异常综合征背景下一种不寻常的核型异常仅在中性粒细胞系列中被检测到。为了鉴定2号染色体的额外拷贝,已将一种通过分选的人类染色体DNA文库进行染色体原位抑制杂交来检测中期细胞中特定人类染色体结构畸变的通用方法应用于11号、3号和2号染色体。