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...

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Detalles Bibliográficos
Autores principales: Wang, Lingling, Tang, Jiao, Feng, Jun, Huang, Yongfen, Cheng, Yuexin, Xu, Hao, Miao, Yuqing
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Immunology
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

Internet

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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