Deciphering Genetic Alterations of Hairy Cell Leukemia and Hairy Cell Leukemia-like Disorders in 98 Patients

Deciphering Genetic Alterations of Hairy Cell Leukemia and Hairy Cell Leukemia-like Disorders in 98 Patients

Hairy cell leukemia (cHCL) patients have, in most cases, a specific clinical and biological presentation with splenomegaly, anemia, leukopenia, neutropenia, monocytopenia and/or thrombocytopenia, identification of hairy cells that express CD103, CD123, CD25, CD11c and identification of the V600E mut...

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Bibliographic Details
Main Authors: Arsham, J. (Author), Benabed, K. (Author), Bijou, F. (Author), Cornet, E. (Author), Jardin, F. (Author), Kerneves, P. (Author), Lebecque, B. (Author), Maitre, E. (Author), Naguib, D. (Author), Sola, B. (Author), Tomowiak, C. (Author), Troussard, X. (Author), Viailly, P.-J (Author)
Format: Article
Language:English
Published: MDPI 2022
Subjects:
BRAF
genetic alterations
hairy cell leukemia
hairy cell leukemia variant (vHCL)
hairy cell leukemia-like disorders
HCL
KLF2
MAP2K1
splenic diffuse red pulp lymphoma (SDRPL)
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