Haseyama Yoshihito, Takeda Yukari, Kumano Koki
Department of Hematology, Tonan Hospital.
Rinsho Ketsueki. 2018;59(12):2594-2599. doi: 10.11406/rinketsu.59.2594.
An 80-year-old female with fever, edema in the lower extremities, and marked eosinophilia was referred to our hospital. Based on the presence of the Philadelphia chromosome, she was diagnosed with chronic myeloid leukemia (CML). Although imatinib induced a complete cytogenetic response (CCyR), CML relapsed after 28 months of starting it. A CCyR was achieved again by nilotinib but was lost after about 14 months. Only transient response occurred to dasatinib, and the patient died. At relapse, neutrophilia was more predominant than eosinophilia. We reviewed 6 patients with CML whose eosinophil rate in the peripheral blood was >50%. Most patients were males with palpable splenomegaly and had cardiac disorders, peripheral vascular disease, or pleural effusion. Typically, CML causes neutrophil-predominant leukocytosis. However, a subgroup of CML with marked eosinophilia resembles chronic eosinophilic leukemia or idiopathic hypereosinophilic syndrome.
一名80岁女性,伴有发热、下肢水肿及明显嗜酸性粒细胞增多,被转诊至我院。基于费城染色体的存在,她被诊断为慢性髓性白血病(CML)。尽管伊马替尼诱导了完全细胞遗传学缓解(CCyR),但在开始使用28个月后CML复发。尼洛替尼再次实现了CCyR,但约14个月后又消失。达沙替尼仅产生短暂反应,患者死亡。复发时,中性粒细胞增多比嗜酸性粒细胞增多更显著。我们回顾了6例外周血嗜酸性粒细胞率>50%的CML患者。大多数患者为男性,可触及脾肿大,并有心脏疾病、外周血管疾病或胸腔积液。典型地,CML引起以中性粒细胞为主的白细胞增多。然而,一组伴有明显嗜酸性粒细胞增多的CML类似于慢性嗜酸性粒细胞白血病或特发性高嗜酸性粒细胞综合征。