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骨髓增生异常综合征患者的染色体分析:与骨髓组织病理学的相关性及预后意义

Chromosome analyses in patients with myelodysplastic syndromes: correlation with bone marrow histopathology and prognostic significance.

作者信息

Werner M, Maschek H, Kaloutsi V, Choritz H, Georgii A

机构信息

Pathologisches Institut, Medizinischen Hochschule Hannover, Federal Republic of Germany.

出版信息

Virchows Arch A Pathol Anat Histopathol. 1992;421(1):47-52. doi: 10.1007/BF01607138.

Abstract

Chromosome analyses of bone marrow and peripheral blood cells were performed in a total of 51 patients with myelodysplastic syndromes (MDS) simultaneously with histopathological examination of resin-embedded bone marrow biopsies. Diagnosis of MDS was established by histopathology according to the French-American-British (FAB) classification, and reassessed by haematological data and clinical course. Clonal karyotypic changes were found in 30 of the 51 patients (59%): in 15 of 19 (79%) patients with refractory anaemia, 7 of 11 (64%) with refractory anaemia and excess of blasts (RAEB), 6 of 10 (60%) with RAEB in transformation, and 2 of 11 (18%) with chronic myelomonocytic leukaemia. The following three features of the histopathology revealed positive correlations with karyotype abnormalities: all cases of myelofibrosis in MDS (7/51) were accompanied by chromosome aberrations, microforms of megakaryocytes with reduced nuclear lobulation were observed in 18 of 30 cases with karyotype changes, and hypocellularity of haematopoiesis was associated with aberrations of chromosome 7 in 2 of 4 cases. No positive correlations were revealed between abnormal karyotypes and the transformation to acute leukaemia. The survival times were significantly decreased in patients with complex (3 and more) karyotype changes, when compared with patients with single (1-2) chromosome aberrations or normal karyotype, independently of the FAB classification.

摘要

对51例骨髓增生异常综合征(MDS)患者的骨髓和外周血细胞进行了染色体分析,同时对树脂包埋的骨髓活检组织进行了组织病理学检查。MDS的诊断根据法国-美国-英国(FAB)分类标准通过组织病理学确定,并通过血液学数据和临床病程进行重新评估。51例患者中有30例(59%)发现克隆性核型改变:19例难治性贫血患者中有15例(79%),11例难治性贫血伴原始细胞增多(RAEB)患者中有7例(64%),10例转化中的RAEB患者中有6例(60%),11例慢性粒-单核细胞白血病患者中有2例(18%)。组织病理学的以下三个特征与核型异常呈正相关:MDS中的所有骨髓纤维化病例(7/51)均伴有染色体畸变,30例核型改变的病例中有18例观察到核叶减少的巨核细胞微形态,4例病例中有2例造血细胞减少与7号染色体畸变有关。异常核型与向急性白血病的转化之间未发现正相关。与具有单一(1-2个)染色体畸变或正常核型的患者相比,具有复杂(3个及以上)核型改变的患者的生存时间显著缩短,且与FAB分类无关。

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