Kaneko Hiroto, Shimura Kazuho, Yoshida Mihoko, Ohkawara Yasuo, Ohshiro Muneo, Tsutsumi Yasuhiko, Iwai Toshiki, Horiike Shigeo, Yokota Shohei, Taniwaki Masafumi
Department of Hematology, Japanese Red Cross Kyoto Daiichi Hospital, 15-749 Honmachi, Higashiyama-ku, Kyoto, 605-0981 Japan.
Department of Hematology, Aiseikai Yamashina Hospital, 19-4 Takehana-Shichono-cho, Yamashina-ku, Kyoto, 607-8086 Japan.
Indian J Hematol Blood Transfus. 2014 Sep;30(Suppl 1):80-3. doi: 10.1007/s12288-013-0255-2. Epub 2013 Apr 26.
We describe a 57-year-old woman who was diagnosed as precursor B-cell acute lymphoblastic leukemia with marked eosinophilia (ALL-eo). She presented with low grade fever and eosinophilia (absolute count 16.5 × 10(9)/l). Most of eosinophils had hypogranular cytoplasm. Immature cells were absent in her peripheral blood. Since her platelet count was low, bone marrow examination was carried out. 57.2 % of nucleated cells were blastic cells positive for CD10, 19, and 20. Chromosomal analysis revealed a karyotype of 46,XX,t(5;14)(q31;q32). Despite induction chemotherapy, her disease progressed and she died of sepsis a month later. ALL-eo is extremely rare and the diagnosis might be delayed unless leukemic cells are seen in peripheral blood. Therefore, bone marrow should be examined as soon as possible in cases with eosinophilia not only for the differential diagnosis of eosinophilic disorders but also not to overlook ALL-eo.
我们描述了一名57岁女性,她被诊断为伴有明显嗜酸性粒细胞增多的前体B细胞急性淋巴细胞白血病(ALL-eo)。她表现为低热和嗜酸性粒细胞增多(绝对计数为16.5×10⁹/L)。大多数嗜酸性粒细胞的细胞质颗粒减少。其外周血中未出现幼稚细胞。由于她的血小板计数较低,因此进行了骨髓检查。57.2%的有核细胞为CD10、19和20阳性的原始细胞。染色体分析显示核型为46,XX,t(5;14)(q31;q32)。尽管进行了诱导化疗,她的病情仍进展,一个月后死于败血症。ALL-eo极为罕见,除非在外周血中发现白血病细胞,否则诊断可能会延迟。因此,对于嗜酸性粒细胞增多的病例,应尽快进行骨髓检查,不仅用于嗜酸性粒细胞疾病的鉴别诊断,也为了不遗漏ALL-eo。