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患者,男,48岁,主因确诊急性粒细胞白血病M1型6个月余,完全缓解4个月余,患者出现间断头痛,伴左眼视物重影,为进一步化疗于2013-06-24入院。患者于6个月前无明显诱因出现全身散在瘀斑,颜色加重,血常规:WBC 292.5×109/L,白细胞无法分类,Hb 76g/L,PLT 11×109/L;血涂片检查:可见大量原始细胞,约占91%;骨髓涂片细胞形态学检查:骨髓增生明显活跃,粒系增生显著,
The patient, male, aged 48, was diagnosed with acute myeloid leukemia for more than 6 months with complete remission for more than 4 months. The patient developed intermittent headache with left-eye ghosting and was admitted for further chemotherapy on June 26, 2013 . Patients with no obvious incentive 6 months ago appeared systemic scattered ecchymosis, color, blood: WBC 292.5 × 109 / L, white blood cells can not be classified, Hb 76g / L, PLT 11 × 109 / L; blood smears: visible A large number of primitive cells, accounting for about 91%; bone marrow smear cells morphology examination: bone marrow hyperplasia was significantly active, granulocyte hyperplasia significantly,