Burkitt Lymphoma - Subtypes, Pathogenesis, and Treatment Strategies. Academic Article uri icon

Overview

abstract

  • Burkitt's lymphoma (BL) is a rare and highly aggressive Non-Hodgkin lymphoma (NHL) with a germinal center phenotype, a nearly universal myc oncogene translocation to an enhancer element and a proliferation index greater than 95%.1 Bcl-2 is not expressed as opposed to double-hit or triple-hit lymphoma. Genetic mutations and aberrancy involving the phosphatidylcholine 3-kinase and cyclin-dependent kinase pathways are also involved.2-5 Rarely patients present with stage I disease and others are considered as high risk if greater than stage I or with elevated LDH or masses greater than 10 cm.

publication date

  • September 1, 2020

Research

keywords

  • Burkitt Lymphoma

Identity

Scopus Document Identifier

  • 85089816828

Digital Object Identifier (DOI)

  • 10.1016/S2152-2650(20)30455-9

PubMed ID

  • 32862862

Additional Document Info

volume

  • 20 Suppl 1