Robyn Jamie, Noel Pierre, Wlodarska Iwona, Choksi Mamta, O'neal Patricia, Arthur Diane, Dunbar Cynthia, Nutman Thomas, Klion Amy
Hematology Branch, National Heart Lung and Blood Institute National Institutes of Health Bethesda, MD 20892, USA.
Leuk Lymphoma. 2004 Dec;45(12):2497-501. doi: 10.1080/10428190400005288.
Hypereosinophilia is a rare presenting sign of acute lymphocytic leukemia. A 29-year-old male was diagnosed with idiopathic hypereosinophilic syndrome with respiratory symptoms. Although his peripheral blood eosinophilia decreased in response to treatment with imatinib mesylate, a follow-up bone marrow showed a diffuse infiltrate of myeloperoxidase-negative blasts. He was subsequently diagnosed with CD10 positive precursor B lymphoblastic leukemia. This case underscores the importance of follow-up bone marrow examination in patients who demonstrate imatinib mesylate-responsive eosinophilia.
嗜酸性粒细胞增多是急性淋巴细胞白血病罕见的表现体征。一名29岁男性被诊断为患有伴有呼吸道症状的特发性嗜酸性粒细胞增多综合征。尽管他的外周血嗜酸性粒细胞增多在接受甲磺酸伊马替尼治疗后有所下降,但后续的骨髓检查显示髓过氧化物酶阴性原始细胞弥漫浸润。他随后被诊断为CD10阳性前体B淋巴细胞白血病。该病例强调了对甲磺酸伊马替尼治疗反应性嗜酸性粒细胞增多患者进行骨髓检查随访的重要性。