Shah I, Lewkow L M, Koppitch F
Am J Med. 1984 Jun;76(6):1097-9. doi: 10.1016/0002-9343(84)90864-7.
Acute basophilic leukemia was diagnosed in a 61-year-old black woman on the basis of 85 to 90 percent basophils in the peripheral blood as well as bone marrow and very high serum histamine level (more than 10,000 ng/ml). These complications occurred as a transformation from essential thrombocythemia. Accompanying this transformation, there was also cytogenetic change from 46XX karyotype to 46XX 2p+ in 66 to 90 percent of cells in the bone marrow. This may be the first reported occurrence of transformation of essential thrombocythemia into acute basophilic leukemia.
一名61岁的黑人女性被诊断为急性嗜碱性粒细胞白血病,其外周血、骨髓中嗜碱性粒细胞占比达85%至90%,且血清组胺水平极高(超过10,000 ng/ml)。这些并发症是由原发性血小板增多症转变而来。伴随这种转变,骨髓中66%至90%的细胞染色体核型也从46XX变为46XX 2p+。这可能是首次报道的原发性血小板增多症转变为急性嗜碱性粒细胞白血病的病例。