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Indian J Cancer ; 2012 Jan-Mar; 49(1): 137-143
Article Dans Anglais | IMSEAR | ID: sea-144564

Résumé

Chronic lymphocytic leukemia (CLL) was largely considered to be a disease of slow progression, standard treatment with Chlorambucil and having almost similar prognosis. With the introduction of molecular methods for understanding the disease pathophysiology in CLL there has been a remarkable change in the approach towards the disease. The variation in B-cell receptor response and immunoglobulin heavy chain variable region (IGHV) mutation, genetic aberration and defect in apoptosis and proliferation has had an impact on therapy initiation and prognosis. Early diagnosis of molecular variant is therefore necessary in CLL.


Sujets)
Aberrations des chromosomes , Humains , Chaines lourdes des immunoglobulines/génétique , Région variable d'immunoglobuline/génétique , Leucémie chronique lymphocytaire à cellules B/diagnostic , Leucémie chronique lymphocytaire à cellules B/génétique , Leucémie chronique lymphocytaire à cellules B/thérapie , Hyperlymphocytose/diagnostic , Mutation , Pronostic , Récepteurs pour l'antigène des lymphocytes B/génétique , Protéine p53 suppresseur de tumeur/génétique , ZAP-70 Protein-tyrosine kinase/génétique
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