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Haematology · Clinical Topics

Lymphoma

⏱️ 30 mins read 📖 Clinical Topics 🎯 MLA Relevance: High

Lymphomas are a diverse group of malignancies arising from the lymphatic system, broadly categorized into Hodgkin Lymphoma (HL) and Non-Hodgkin Lymphoma (NHL). They typically present with painless lymphadenopathy and systemic 'B-symptoms'.

📌 Learning Objectives

  • Describe the key differences between Hodgkin Lymphoma and Non-Hodgkin Lymphoma.
  • Explain the significance of Reed-Sternberg cells in the diagnosis of Hodgkin Lymphoma.
  • Identify the common presenting symptoms and signs of lymphoma, including 'B-symptoms'.
  • Outline the diagnostic approach to suspected lymphoma, emphasising the role of excision biopsy.
  • Apply the Ann Arbor staging system to clinical scenarios of lymphoma.

📋 Overview

Hodgkin Lymphoma (HL) is characterized by the presence of Reed-Sternberg (RS) cells and typically follows an orderly spread through lymph node chains. It has a bimodal age distribution (peaks at 20-30 and 70-80). Non-Hodgkin Lymphoma (NHL) is a more heterogeneous group (85% B-cell, 15% T-cell) and includes indolent types like Follicular Lymphoma and aggressive types like Diffuse Large B-Cell Lymphoma (DLBCL) or Burkitt Lymphoma. Staging for both is conducted using the Ann Arbor system. Presentation often includes painless, rubbery lymphadenopathy, fever, night sweats, and weight loss (B-symptoms). In HL, pain in lymph nodes after drinking alcohol is a rare but classic symptom. Diagnosis requires an excision node biopsy; fine-needle aspiration (FNA) is usually insufficient for architecture assessment.

🔬 Basic Science

Lymphomas result from genetic mutations in lymphocytes at various stages of maturation. HL involves a small number of malignant B-cells (Reed-Sternberg cells) surrounded by a massive infiltrate of reactive non-malignant inflammatory cells. RS cells are typically CD15 and CD30 positive. NHL involves the clonal expansion of B-cells or T-cells. Risk factors include immunosuppression (HIV, post-transplant), autoimmune diseases (Sjogren's, Hashimoto's), and viral infections (EBV for HL and Burkitt; HTLV-1 for Adult T-cell leukaemia/lymphoma; H. pylori for MALT lymphoma). Burkitt lymphoma involves the c-myc oncogene.

🏥 Clinical Relevance

Painless lymphadenopathy is the most common presentation, often cervical. B-symptoms are significant for prognosis and staging. HL: Mediastinal masses are common (can cause SVC obstruction) and pruritus is a frequent symptom. NHL: Variable presentation; aggressive types present with rapidly enlarging nodes; indolent types with years of waxing and waning nodes. Extranodal involvement (skin, GI tract, brain) is more common in NHL. Burkitt lymphoma (endemic form) typically presents with a jaw mass.

🧪 Investigations

Bedside: Full physical exam of all node stations and organomegaly. Bloods: FBC, ESR (prognostic in HL), LDH (marker of cell turnover and prognostic in NHL), Liver function, HIV/HBV/HCV screening. Gold Standard: Lymph node excision biopsy (Morphology and Immunohistochemistry). Imaging: CT Chest/Abdomen/Pelvis and PET-CT for staging (PET is essential in HL). Bone marrow biopsy: To assess for Stage IV disease.

💊 Management

Hodgkin Lymphoma: ABVD chemotherapy (Adriamycin, Bleomycin, Vinblastine, Dacarbazine) + Radiotherapy for early stage. Risk of long-term radiotherapy complications (breast cancer, lung cancer, hypothyroidism). Non-Hodgkin Lymphoma (Aggressive): R-CHOP (Rituximab, Cyclophosphamide, Hydroxydaunorubicin, Oncovin/Vincristine, Prednisolone). Non-Hodgkin Lymphoma (Indolent): Often 'watch and wait' if asymptomatic; Rituximab + chemotherapy (e.g., Bendamustine) when progressive. Supportive: Flu vaccine, prophylactic acyclovir/co-trimoxazole during chemo.

Revision Resources – expand the sections below for high-yield notes, exam pearls, key facts and further reading.

🎯 MLA High-Yield Notes & Quick Revision
Exam pearl: Alcohol-induced node pain = HL. Starry sky appearance on biopsy = Burkitt Lymphoma. If the question mentions a painless node that has been there for weeks and doesn't move, think lymphoma. Reed-Sternberg cells look like 'owl's eyes'.
Lymphadenopathy Weight loss Fever of unknown origin Night sweats Anaemia Splenomegaly
  • Lymphoma is a cancer of the lymphatic system.
  • Divided into Hodgkin Lymphoma (HL) and Non-Hodgkin Lymphoma (NHL).
  • HL features Reed-Sternberg cells and has a bimodal age distribution.
  • NHL is more common, heterogeneous, and often B-cell origin.
  • Common presentation: painless lymphadenopathy, B-symptoms (fever, night sweats, weight loss).
  • Diagnosis requires excision biopsy for histological and architectural assessment.
Exam Pearls
⭐ High Yield
Painless lymphadenopathy is the most common presenting symptom of lymphoma.
B-symptoms (fever, night sweats, weight loss) indicate systemic disease and are prognostically significant.
Hodgkin Lymphoma is characterised by Reed-Sternberg cells and has a bimodal age distribution.
Non-Hodgkin Lymphoma is more common and heterogeneous, with most cases being B-cell origin.
Excision biopsy is crucial for lymphoma diagnosis, as FNA is often insufficient.
The Ann Arbor staging system is used for both HL and NHL.
💡 Clinical Pearl
Infectious Mononucleosis: Can cause lymphadenopathy and B-symptoms, mimicking lymphoma, but is self-limiting and has different serology.
Tuberculosis: Can present with chronic lymphadenopathy, fever, and weight loss, requiring differentiation from lymphoma.
HIV/AIDS: Patients are at increased risk of developing certain types of Non-Hodgkin Lymphoma.
⚠️ Exam Tip — Common Mistakes
Confusing Hodgkin and Non-Hodgkin Lymphoma characteristics, especially regarding Reed-Sternberg cells.
Believing FNA is sufficient for lymphoma diagnosis; it's usually not, due to architectural requirements.
Forgetting the significance of 'B-symptoms' in staging and prognosis.
Not considering lymphoma in younger patients presenting with persistent lymphadenopathy.
Attributing all lymphadenopathy to infection without considering malignancy.
🔑 Key Facts
HL is defined by the Reed-Sternberg cell ('owl's eyes').
NHL is more common and increases in incidence with age.
Ann Arbor Staging: I (one node), II (two nodes same side of diaphragm), III (both sides), IV (extra-nodal).
B-symptoms: Weight loss >10% in 6 months, drenching night sweats, fever >38°C.
Diagnosis requires a tissue biopsy (Excision biopsy is gold standard).
Burkitt Lymphoma is associated with EBV and t(8;14) translocation.
Prognosis for HL is generally very good with modern chemotherapy.
🔗 Related Topics
📚 References
  1. NICE CKS - Lymphoma
  2. British Society for Haematology - Guidelines for HL/NHL
  3. Kumar & Clark's Clinical Medicine

Further Resources

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