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Essential thrombocythemia during treatment of acute myeloid leukemia with JAK2 V617F mutation: A case report of a CARE-compliant article
RATIONALE: The JAK2 V617F mutation is frequently found in ET, while it is rare in de novo AML. ET has a low frequency of leukemic transformation. Both secondary AML (sAML) from ET and AML with JAK2 V617F mutation have poor prognoses. Because of the low incidence of JAK2 mutation in acute myeloid leu...
Autores principales: | Ding, Wenwen, Li, Danni, Zhuang, Chao, Wei, Pingping, Mou, Wenfeng, Zhang, Lei, Liang, Hui, Liu, Yong |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Wolters Kluwer Health
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6076173/ https://www.ncbi.nlm.nih.gov/pubmed/29979407 http://dx.doi.org/10.1097/MD.0000000000011331 |
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