Enright H, Weisdorf D, Peterson L, Rydell R E, Kaplan M E, Arthur D C
Department of Medicine, University of Minnesota, Minneapolis.
Leukemia. 1992 May;6(5):381-4.
Abnormalities of chromosome 16, including inv(16)(p13q22), del(16)(q22), and t(16;16)(p13;q22), have been reported almost exclusively in association with acute myelomonocytic leukemia and are characteristically accompanied by abnormal eosinophils with dysplastic granules in the bone marrow. We observed an inv(16)(p13q22) in two patients with typical Philadelphia chromosome positive chronic myeloid leukemia (CML). The appearance of the abnormality of chromosome 16 was associated with acceleration of disease or onset of blast crisis and with the appearance in the bone marrow of abnormal eosinophils. In both cases the marrow karyotypes were 46,XY,t(9;22)(q34;q11)/46,XY,inv(16)(p13q22),t(9;22)(q34;q11). In these two patients the temporal association of the acquisition of the inversion 16 and the appearance of monocytoid cells and dysplastic eosinophils in the bone marrow further supports the relationship of this karyotypic abnormality with leukemic monocytoid and eosinophilic evolution. This secondary cytogenetic change appears to be an infrequent manifestation of specific phenotypic disease progression in CML.
16号染色体异常,包括inv(16)(p13q22)、del(16)(q22)和t(16;16)(p13;q22),几乎仅在急性粒单核细胞白血病中报道过,其特征是骨髓中伴有异常嗜酸性粒细胞和发育异常的颗粒。我们在两名典型的费城染色体阳性慢性髓性白血病(CML)患者中观察到inv(16)(p13q22)。16号染色体异常的出现与疾病加速或急变期的发生以及骨髓中异常嗜酸性粒细胞的出现有关。在这两例中,骨髓核型均为46,XY,t(9;22)(q34;q11)/46,XY,inv(16)(p13q22),t(9;22)(q34;q11)。在这两名患者中,16号染色体倒位的获得与骨髓中单核样细胞和发育异常的嗜酸性粒细胞出现的时间相关性,进一步支持了这种核型异常与白血病单核样和嗜酸性粒细胞演变的关系。这种继发性细胞遗传学改变似乎是CML中特定表型疾病进展的罕见表现。