Handa Hiroshi, Motohashi Sachiko, Isozumi Kazuo, Komatsumoto Satoru, Nara Masaharu
Third Department of Internal Medicine, Gunma University School of Medicine, Maebashi, Gunma, Japan.
Acta Haematol. 2002;108(1):47-52. doi: 10.1159/000063065.
We describe a 69-year-old Japanese male with acute leukemia with a CD7+ and CD56+ immunophenotype presenting with multiple lymphadenopathy. He was treated with idarubicin and cytosine arabinoside. Although the leukemia showed partial response, the patient did not achieve complete remission. He died of sepsis due to severe neutropenia after the third course of chemotherapy. His autopsy revealed blast infiltration in the lymph nodes, liver, spleen and vertebral bone marrow. Recently, CD7+ and CD56+ myeloid/natural killer precursor acute leukemia has been associated with a poor prognosis. Our case illustrates that myeloid/natural killer cell precursor acute leukemia shows some response to intensive chemotherapy for acute myeloid leukemia, but such therapy is insufficient to effect a cure. To overcome the resistance of this disease to chemotherapy, further studies should explore other treatment strategies.
我们描述了一名69岁的日本男性,患有急性白血病,免疫表型为CD7+和CD56+,表现为多处淋巴结病。他接受了伊达比星和阿糖胞苷治疗。尽管白血病显示出部分缓解,但患者未达到完全缓解。在第三个化疗疗程后,他因严重中性粒细胞减少死于败血症。尸检发现其淋巴结、肝脏、脾脏和脊椎骨髓有原始细胞浸润。最近,CD7+和CD56+髓系/自然杀伤前体急性白血病与预后不良有关。我们的病例表明,髓系/自然杀伤细胞前体急性白血病对急性髓系白血病的强化化疗有一定反应,但这种治疗不足以治愈。为克服这种疾病对化疗的耐药性,进一步的研究应探索其他治疗策略。