Shah-Reddy I, Mirchandani I, Bishop C R
Cancer. 1981 Feb 15;47(4):715-9. doi: 10.1002/1097-0142(19810215)47:4<715::aid-cncr2820470415>3.0.co;2-6.
Acute lymphoblastic leukemia (ALL) with hand mirror cell (HMC) variant was diagnosed in a 26-year-old black man in May 1978. Hemoglobin was 3.6 g/dl; the platelet count was 19.0 x 10(9)/l; leukocyte count was 8.4 x 10(9)/l with 40% blasts, 66% of which had HMC appearance. Cytochemical studies, terminal deoxynucleotidyl transferase level, and immunologic marker studies indicated a non-T/non-B lymphoblastic origin of the leukemic population. Electron microscopic studies confirmed the hand mirror appearance. Mitochondria were more numerous in these cells compared with other lymphoid cells. Cytogenetic studies showed a 46XY karyotype. Our studies confirmed the previous studies reported by Stass, et al of lymphoblastic origin of HMC leukemia. The patient responded to treatment with vincristine, prednisone and L-asparaginase and went into complete remission. It appears that this morphologic variant of ALL does exist and is not an artifact.
1978年5月,一名26岁的黑人男性被诊断为伴有手镜细胞(HMC)变异型的急性淋巴细胞白血病(ALL)。血红蛋白为3.6 g/dl;血小板计数为19.0×10⁹/l;白细胞计数为8.4×10⁹/l,其中40%为原始细胞,66%具有HMC外观。细胞化学研究、末端脱氧核苷酸转移酶水平及免疫标志物研究表明白血病细胞群起源于非T/非B淋巴细胞。电子显微镜研究证实了手镜外观。与其他淋巴细胞相比,这些细胞中的线粒体更多。细胞遗传学研究显示核型为46XY。我们的研究证实了Stass等人之前报道的关于HMC白血病起源于淋巴细胞的研究。患者对长春新碱、泼尼松和L-天冬酰胺酶治疗有反应并进入完全缓解期。看来ALL的这种形态学变异确实存在,并非人为现象。