A Case of Myeloid Sarcoma with Correlation to JAK2V617F Mutation, Complicated by Myelofibrosis and Secondary Acute Myeloid Leukemia
Author:
Affiliation:
1. Department of Hematology and Oncology, Graduate School of Medicine, University of Tokyo, Japan
2. Department of Pathology, University of Tokyo Hospital, Japan
Publisher
Japanese Society of Internal Medicine
Subject
General Medicine,Internal Medicine
Link
http://www.jstage.jst.go.jp/article/internalmedicine/50/21/50_21_2649/_pdf
Reference16 articles.
1. A Gain-of-Function Mutation ofJAK2in Myeloproliferative Disorders
2. Identification of an Acquired JAK2 Mutation in Polycythemia Vera
3. 3. Levine RL, Wadleigh M, Cools J, et al. Activating mutation in the tyrosine kinase JAK2 in polycythemia vera, essential thrombocythemia, and myeloid metaplasia with myelofibrosis. Cancer Cell 7: 387-397, 2005.
4. A unique clonal JAK2 mutation leading to constitutive signalling causes polycythaemia vera
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