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Case report: A rare case of coexisting Waldenstrom Macroglobulinemia and B-cell acute lymphoblastic leukemia with KMT2D and MECOM mutations
BACKGROUND: Waldenstrom Macroglobulinemia (WM) is a rare and indolent lymphoma of B-cell origin characterized by elevated monoclonal IgM, with MYD88L265P mutation and CXCR4 mutation as common molecular alterations. B-cell Acute Lymphoblastic Leukemia (B-ALL) is clinically heterogeneous, characterize...
Autores principales: | Wang, Lingling, Tang, Jiao, Feng, Jun, Huang, Yongfen, Cheng, Yuexin, Xu, Hao, Miao, Yuqing |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9618799/ https://www.ncbi.nlm.nih.gov/pubmed/36325357 http://dx.doi.org/10.3389/fimmu.2022.1001482 |
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