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General Medicine

Hodgkin Lymphoma

A highly curable lymphatic cancer marked by painless swollen lymph nodes and the presence of unique Reed-Sternberg cells.

Source: WHO / CDC / NIH Evidence Guidelines
Updated: Aug 14, 2026
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Red Flag Warning & Emergency Situations

Emergency Management: Superior Vena Cava (SVC) Syndrome from large mediastinal mass. Treat with steroids/radiation.

Core Definition:

Hodgkin Lymphoma (HL) is a B-cell malignancy characterized by sparse, multinucleated Reed-Sternberg (RS) cells embedded in a dense background of reactive inflammatory cells.

Detailed Overview

HL classically spreads contiguously through lymph node chains. It has a bimodal age distribution (20-30s and >65). It is highly curable with multi-agent chemotherapy (ABVD) and involved-site radiation, though treatment is associated with significant long-term toxicities like secondary cancers and cardiotoxicity.

Epidemiology & Demographics

Incidence of 2.5 per 100,000. Nodular sclerosis is the most common subtype in young adults.

Etiological Mechanism

EBV infection is implicated in 40-50% of classical HL cases.

Primary Causes

Malignant transformation of germinal center B-cells

Malignant RS cells secrete cytokines (IL-5, TARC) recruiting benign lymphocytes and eosinophils, which make up 98% of the tumor. RS cells express PD-L1, exhausting host T-cells and enabling immune evasion.

Diagnostic Criteria & Guidelines

Excisional lymph node biopsy showing Reed-Sternberg cells with appropriate IHC.

First-Line Treatment:

Advanced stage: ABVD (Doxorubicin 25 mg/m2, Bleomycin 10 U/m2, Vinblastine 6 mg/m2, Dacarbazine 375 mg/m2) for 6 cycles. Often adapted based on interim PET/CT (dropping Bleomycin).

Second-Line & Adjunctive Therapy

Salvage chemotherapy (ICE) followed by Autologous Stem Cell Transplant.

Surgical & Procedural Management

Excisional biopsy for diagnosis. No therapeutic surgery.

Patient Counseling & Advice

Discuss high cure rates. Instruct to report fever >38.3°C immediately due to neutropenia. Warn of temporary hair loss.

Follow-Up & Monitoring Schedule

H&P every 3-6 months. Annual TSH if neck radiated. Mammogram/MRI at age 40 or 8 years post-chest radiation.

Preventive Strategies

No primary prevention.

Excellent. 5-year survival is ~89%.

Authoritative Sources & Evidence References
World Health Organization (WHO) & CDC Guidelines: Information compiled from current international clinical practice guidelines.

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