Keung Y K, Pettenati M J, Cruz J M, Powell B L, Woodruff R D, Buss D H
Section on Hematology-Oncology, Department of Medicine, Comprehensive Cancer Center of Wake Forest University, Winston-Salem, North Carolina, USA.
Am J Hematol. 2001 Mar;66(3):167-71. doi: 10.1002/1096-8652(200103)66:3<167::aid-ajh1040>3.0.co;2-r.
Cytogenetic abnormalities in association with aplastic anemia have been reported fairly infrequently. Clonal cytogenetic abnormalities at initial diagnosis are uncommon. A retrospective study was performed of the cytogenetic findings in patients with typical morphological and clinical features of severe aplastic anemia from a single institution for the years 1988 through 1998. A total of 30 cases of aplastic anemia, 16 men and 14 women, were identified. The median age was 60 with females being significantly older (67.5 years) in comparison to males (44 years). Bone marrow specimens failed to yield metaphases in 16 cases and normal karyotypes were detected in 11 cases. Cytogenetic abnormalities were detected in 3 cases. Clonal abnormalities, as defined, occurred in only 2 cases (6.7%). A review of the literature identified a total of 24 cases of aplastic anemia with abnormal cytogenetic findings. Overall, the most common chromosome abnormalities are trisomies of 6 and 8 and loss of chromosome 7. Trisomy 6 is more common at diagnosis while loss of chromosome 7 is more common after therapy.
与再生障碍性贫血相关的细胞遗传学异常报道相对较少。初诊时的克隆性细胞遗传学异常并不常见。对1988年至1998年期间来自单一机构的具有典型形态学和临床特征的重型再生障碍性贫血患者的细胞遗传学结果进行了一项回顾性研究。共确定了30例再生障碍性贫血患者,其中16例男性,14例女性。中位年龄为60岁,女性(67.5岁)明显比男性(44岁)年龄大。16例骨髓标本未能获得中期分裂相,11例检测到正常核型。3例检测到细胞遗传学异常。按照定义,克隆性异常仅发生在2例(6.7%)。文献回顾共发现24例再生障碍性贫血伴有异常细胞遗传学结果。总体而言,最常见的染色体异常是6号和8号染色体三体以及7号染色体缺失。6号染色体三体在诊断时更常见,而7号染色体缺失在治疗后更常见。