医学
达沙替尼
骨髓纤维化
鲁索利替尼
髓系白血病
克隆(Java方法)
内科学
髓样
Janus激酶2
肿瘤科
骨髓
癌症研究
胃肠病学
伊马替尼
基因
化学
受体
生物化学
作者
Ayae Amemiya,Yoshikazu Ito,Yasunori Ishibashi,Yuu Saito,Seiichiro Katagiri,Tamiko Suguro,Michiyo Asano,Seiichiro Yoshizawa,Daigo Akahane,Yuko Tanaka,Hiroaki Fujimoto,Seiichi Okabe,Moritaka Gotoh,Tetsuzo Tauchi,Kazuma Ohyashiki
出处
期刊:PubMed
日期:2017-01-01
卷期号:58 (4): 298-302
标识
DOI:10.11406/rinketsu.58.298
摘要
A 53-year-old woman with a 27-year history of myeloproliferative neoplasms came to our hospital because of a marked white blood cell count increase and progressive anemia. Clinical examination demonstrated positivity for BCR-ABL1 and JAK2-V617F mutations. She was given a diagnosis of chronic myeloid leukemia. Using the international scale, a molecular response (MR) 4.5 was achieved after treatment with dasatinib, despite the persistence of marked splenomegaly. The pathological findings of myelofibrosis were demonstrated by bone marrow biopsy. After stopping dasatinib administration for 4 years and 5 months, treatment with ruxolitinib was started. Five months later, the size of her spleen was reduced. We speculated that translocation of BCR-ABL1 might have occurred in a sub-clone of the JAK2-V617F mutated tumor clone.
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