Kowal-Vern A, Birdsong B A, Dizikes G, Radvany R, Desai S N, Schumacher H
Department of Pathology, Loyola University Medical Center, Maywood, Ill 60153.
Arch Pathol Lab Med. 1990 Jul;114(7):676-8.
We present, to our knowledge, the first extensively studied case of lymphoid L2 blast crisis of chronic myelogenous leukemia with a hand mirror cell (HMC) variant. Special stains revealed the leukemic cells to be terminal deoxynucleotidyl transferase positive by immunofluorescence and cytochemically positive for alpha-naphthyl acetate esterase and acid phosphatase (diffuse granular). Immunophenotyping identified the major leukemic cell population as B-cells that expressed CD10+, CD19+, and HLA-DR+. It was not possible to separate the HMC and the non-HMC leukemic population by gating various cell populations, dual staining, cytochemistry, or by terminal deoxynucleotidyl transferase. Gene rearrangements were observed in both Ig heavy-chain alleles and one T-cell antigen receptor gamma-subunit allele. The rearrangements occupied all of the cells, indicating that the HMC and non-HMC were of a common clonal origin. The patient had a mosaic karyotype, with 90% of the cells having t(9;22), t(8;14), and t(9;15) translocations, an additional chromosome 8, and deleted chromosomes 9 and 15. Antibodies to simian sarcoma-associated virus and baboon endogenous virus were isolated in the patient's peripheral blood plasma.
据我们所知,我们首次对一例伴有手镜细胞(HMC)变异型的慢性髓性白血病淋巴样L2原始细胞危象进行了广泛研究。特殊染色显示,白血病细胞经免疫荧光检测末端脱氧核苷酸转移酶呈阳性,细胞化学检测对α-萘乙酸酯酶和酸性磷酸酶呈阳性(弥漫性颗粒状)。免疫表型分析确定主要的白血病细胞群体为表达CD10 +、CD19 +和HLA-DR +的B细胞。通过对各种细胞群体进行门控、双重染色、细胞化学或末端脱氧核苷酸转移酶,无法分离HMC和非HMC白血病细胞群体。在Ig重链等位基因和一个T细胞抗原受体γ亚基等位基因中均观察到基因重排。重排存在于所有细胞中,表明HMC和非HMC具有共同的克隆起源。该患者具有嵌合核型,90%的细胞具有t(9;22)、t(8;14)和t(9;15)易位、一条额外的8号染色体以及9号和15号染色体缺失。在患者外周血浆中分离出了抗猿猴肉瘤相关病毒和狒狒内源性病毒的抗体。