Non-Hodgkin lymphomas

Epidemiology


Etiology


Pathophysiology

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Clinical features

Indolent (low-grade)

Aggressive (high-grade)


Diagnostics

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Lymphoma arises from mature lymphocytes and often forms tumors in the lymphatic system, leukemia typically originates from immature progenitor cells in the bone marrow and is characterized by abnormal cells circulating in the blood.

Chromosomal translocations

Malignancy Pathogenesis
Acute promyelocytic leukemia t(15;17) involving PML & RARA → PML-RARα oncoprotein → myeloid differentiation inhibited
RARα: nuclear receptor involved in myeloid differentiation
PML: fusion forms receptor with dominant negative activity
Burkitt lymphoma t(8;14) involving MYC & IGH → MYC overexpression → cell growth
MYC: transcription factor regulating cell growth
IGH: immunoglobulin heavy chain (high expression in B cells)
Chronic myeloid leukemia t(9;22) involving ABL1 & BCR → BCR-ABL1 oncoprotein → cell proliferation
ABL1: nonreceptor tyrosine kinase
BCR: fusion leads to activation
Follicular lymphoma t(14;18) involving IGH & BCL2 → BCL2 overexpression → apoptosis evasion
BCL2: antiapoptotic protein
Mantle cell lymphoma t(11;14) involving CCND1 & IGH → cyclin D1 overexpression → cell cycle progression
Cyclin D1: regulates cell cycle progression

Pathology

Treatment


Specific regimens