| Literature DB >> 32323276 |
Xin Meng1, Qing Min1, Ji-Yang Wang2.
Abstract
B cell development and activation are accompanied by dynamic genetic alterations including V(D)J rearrangements and immunoglobulin-gene somatic hypermutation and class-switch recombination. Abnormalities in these genetic events can cause chromosomal translocations and genomic mutations, leading to altered expression and function of genes involved in B cell survival or proliferation and consequently B lymphomagenesis. In fact, B cell lymphoma accounts for 95% of the lymphomas. In this chapter, we summarize the morphology, immunophenotypes, clinical features, genetic defects that cause the malignancies, treatments, and prognosis of the most prevalent types of B cell lymphomas, including typical precursor B cell malignance (B-ALL/LBL) and mature B cell lymphoma (Hodgkin lymphoma and B cell non-Hodgkin lymphoma).Entities:
Keywords: B cell non-Hodgkin lymphoma; B lymphoblastic leukemia/lymphoma; Chromosomal translocation; Hodgkin lymphoma; Molecular target therapy
Mesh:
Year: 2020 PMID: 32323276 DOI: 10.1007/978-981-15-3532-1_12
Source DB: PubMed Journal: Adv Exp Med Biol ISSN: 0065-2598 Impact factor: 2.622