Definition: Lymphoma is a malignancy of lymphocytes arising from lymphoid tissues. It is broadly classified into:
Major Types
- Characterized by Reed–Sternberg cells (CD30+, CD15+)
- Typically affects young adults
- Spread is orderly and predictable
- Heterogeneous group (B-cell > T-cell)
- More variable clinical behavior
- Includes:
- Diffuse Large B-Cell Lymphoma (DLBCL) – aggressive, most common
- Follicular Lymphoma – indolent
- Mantle Cell Lymphoma, Burkitt Lymphoma, T-cell Lymphomas
Clinical Features
- Painless lymphadenopathy (commonly cervical or supraclavicular)
- B symptoms: fever, night sweats, weight loss
- Fatigue, hepatosplenomegaly
- Extranodal involvement (GI, CNS, marrow)
Diagnosis
- Excisional lymph node biopsy (gold standard)
- Immunophenotyping (flow cytometry, IHC)
- PET-CT for staging
- Bone marrow biopsy if indicated
- Cytogenetics/molecular studies (e.g., t(14;18) in follicular lymphoma, MYC in Burkitt)
Staging (Ann Arbor System)
- Stage I–IV based on extent of nodal/extranodal involvement
- “A” = no B symptoms, “B” = presence of B symptoms
- Bulky disease = large mass (>10 cm or >1/3 mediastinum)
Treatment Overview
- ABVD: doxorubicin, bleomycin, vinblastine, dacarbazine
- Consider Brentuximab vedotin (CD30+) or nivolumab (PD-1) in relapse
- Cure rate high, even in advanced stages
- DLBCL: R-CHOP (rituximab, cyclophosphamide, doxorubicin, vincristine, prednisone)
- Follicular lymphoma: rituximab ± chemo or observation
- Burkitt lymphoma: aggressive multi-agent chemo (e.g., hyper-CVAD)
- Mantle cell lymphoma: rituximab + bendamustine or R-HyperCVAD; often transplant
- CNS prophylaxis if high risk (e.g., testicular, breast, high LDH)
Key Pharmacologic Considerations
- Rituximab: anti-CD20 monoclonal antibody; watch for infusion reactions, HBV reactivation
- Chemotherapy toxicity: neutropenia, mucositis, cardiac toxicity (doxorubicin), neuropathy (vincristine)
- Growth factor support (e.g., G-CSF) often needed
- TLS prophylaxis in high-grade NHLs (hydration, allopurinol, rasburicase)
Monitoring
- CBC, renal/hepatic function
- LDH (prognostic marker)
- Interim PET scan for response assessment
- Cardiac monitoring with anthracyclines
- Long-term: secondary malignancy risk, fertility, cardiac function
Prognosis
- HL: >85% cure rate
- NHL: depends on type and stage (e.g., indolent vs aggressive subtypes)
- Use IPI (International Prognostic Index) for NHL risk stratification
Synonyms
Lymphomas

