Taniwaki M, Inazawa J, Horiike S, Misawa S, Abe T, Takino T
Cancer Genet Cytogenet. 1987 Feb;24(2):257-62. doi: 10.1016/0165-4608(87)90107-5.
A 37-year-old Japanese male patient with acute myelomonocytic leukemia subtype M4 (according to FAB classification) associated with bone marrow eosinophilia and specific chromosome abnormalities: a pericentric inversion of chromosome 16, inv(16)(p13q22); a long arm deletion of chromosome #7, del(7)(q22q34); and a gain of chromosomes #8 and #22 is reported. In addition to the modal karyotype, 47,XY,7q-,inv(16),+22, there were three other clones whose karyotypes were 46,XY,inv(16); 47,XY,inv(16),+22; and 48,XY,+8,inv(16),+22. As these karyotypes were related to each other, the presence of multiple clones indicated that karyotypic evolution had occurred. The karyotypic evolution associated with 7q- has not been reported previously in patients with M4Eo with inv(16).
报告了一名37岁的日本男性患者,患有急性粒单核细胞白血病M4亚型(根据FAB分类),伴有骨髓嗜酸性粒细胞增多和特定染色体异常:16号染色体臂间倒位,inv(16)(p13q22);7号染色体长臂缺失,del(7)(q22q34);以及8号和22号染色体增多。除了众数核型47,XY,7q-,inv(16),+22外,还有另外三个克隆,其核型分别为46,XY,inv(16);47,XY,inv(16),+22;以及48,XY,+8,inv(16),+22。由于这些核型相互关联,多个克隆的存在表明发生了核型进化。此前在伴有inv(16)的M4Eo患者中尚未报道与7q-相关的核型进化。