| Literature DB >> 27275640 |
Eszter Sári1, Hajnalka Rajnai2, Kitti Dénes2, Csaba Bödör2, Judit Csomor2, Gábor Körösmezey1, Ilona Tárkányi1, Hanna Eid2, Zsolt Nagy1, Judit Demeter1.
Abstract
Differential diagnosis of hairy cell leukemia (HCL) and related disorders (hairy cell leukemia variant and splenic marginal zone lymphoma) is of utmost importance since the treatment and prognosis of these lymphomas differ. Since 2011 diagnosis of hairy cell leukemia has been easier because of discovery of the disease defining somatic mutation BRAF V600E mutation, which has been also known as driver mutation in malignant melanoma. The presence of this mutation enabled targeted molecular therapy in HCL as well. As first line therapy purine nucleoside analogues are the gold standard, but refractory/relapsed patient are candidates for targeted BRAF-inhibitor therapy. This manuscript serves as guidance in making diagnosis and standard treatment of HCL, and summarizes newest data about molecular therapy, including our single center experience collected from 75 patients.Entities:
Mesh:
Substances:
Year: 2016 PMID: 27275640
Source DB: PubMed Journal: Magy Onkol ISSN: 0025-0244