A.15 Hodgkin's Lymphoma Flashcards
A.15 Hodgkin’s Lymphoma
Epidemiology
Age: Bimodal distribution:
- 1st peak: 25-30 years
- 2nd peak: 50-70 years
Higher incidence in males (especially notable in pediatric cases)
Exeption: nodular sclerosing HL shows a more balanced distribution, with roughly equal rates of diagnosis in males and females.
A.15 Hodgkin’s Lymphoma
In Hodgkin’s lymphoma, characteristic cells with mirror-image nuclei are found, called Reed–Sternberg cells.
Hodgkin’s lymphoma (HL) is a malignancy of mature B lymphocytes.
It represents ~10% of all lymphomas diagnosed each year.
The majority of HL diagnoses are classical HL (cHL), but there is a second subtype of HL, nodular lymphocyte-predominant HL (NLPHL).
A.15 Hodgkin’s Lymphoma
Etiology
Risk Factors:
* Association with Epstein-Barr virus (EBV)
* Immunodeficiency (e.g., organ transplant recipients, HIV infection)
* Autoimmune diseases (e.g., RA, sarcoidosis)
A.15 Hodgkin’s Lymphoma
Clinical Features
- Painless Lymphadenopathy:
* Cervical Lymph Nodes: Affected in 60-70% of patients.
* Axillary Lymph Nodes: Involved in 25-35% of cases.
* Inguinal Lymph Nodes: Affected in 8-15% of patients.
* Mediastinal Lymph Nodes: Can cause chest pain, dry cough, and shortness of breath. - Systemic Symptoms (B Symptoms):
* Night sweats, unexplained weight loss (>10% in 6 months), and fever (>38°C), which may overlap with other diseases. - Other Symptoms:
* Alcohol-Induced Pain: Pain in lymph nodes after consuming alcohol.
* Pruritus: Itching that may be localized or generalized. - Characteristics of Lymphadenopathy:
* Lymph nodes may show rapid growth, be painless, hard/ coarse, and fixed to surrounding tissues, indicating possible malignancy.
A.15 Hodgkin’s Lymphoma
Staging (Ann Arbor System)
- Stage I: Confined to a single lymph node region.
- Stage II: Involvement of two or more nodal areas on the same side of the diaphragm.
- Stage III: Involvement of lymph nodes on both sides of the diaphragm.
- Stage IV: Spread beyond the lymph nodes to the liver or bone marrow.
Each stage can be classified as either
‘A’—without systemic symptoms other than pruritus, or
‘B’—presence of B symptoms: weight loss >10% in the last 6 months, unexplained fever >38°C, or night sweats.
Stage ‘B’ indicates worse disease.
Localized extranodal extension does not change the stage but is noted with a subscript, e.g., I-AE.
The staging of Hodgkin’s lymphoma influences treatment options and prognosis. It is determined through imaging and, if B symptoms or stage III–IV disease are present, a marrow biopsy.
A.15 Hodgkin’s Lymphoma
Diagnostics
Diagnosis of Hodgkin’s lymphoma is primarily based on medical history and clinical features (B symptoms, localization of lymph node involvement) and is confirmed with a lymph node biopsy (excisional).
Blood Tests
* Complete Blood Count (CBC): May show elevated or decreased white blood cell count, anemia, or eosinophilia.
* Serum Chemistry: Elevated LDH; hypercalcemia (potentially due to paraneoplastic syndromes).
* Vitamin D Levels: Check for deficiencies.
Histology
* Obligatory Diagnostic Step: Lymph node biopsy is essential.
* Reed-Sternberg Cells (RSCs): Characteristic cells originating from B cells; positive for CD15/CD30 markers.
Imaging
* Chest X-ray or CT Scan: Used to detect and measure masses and enlarged lymph nodes.
* Bone Scintigraphy or PET-CT: Conducted prior to treatment to assess disease spread.
A.15 Hodgkin’s Lymphoma
Pathology
- Nodular Sclerosis: Most common subtype.
- Lymphocyte Predominance: Associated with the best prognosis.
- Mixed Cellularity: Often shows eosinophilia; seen in immunocompromised patients.
- Lymphocyte Depletion: Typically seen in immunocompromised individuals.
A.15 Hodgkin’s Lymphoma
Differential Diagnosis of Lymphadenopathy
Generalized lymphadenopathy can indicate systemic illnesses such as HIV, mycobacterial infections, or lymphoma (including Hodgkin’s lymphoma).
Symptoms may include tender, mobile, and erythematous lymphadenopathy.
A.15 Hodgkin’s Lymphoma
Treatment
Early Stage (I and II):
Combination of chemotherapy and radiation therapy.
Chemotherapy Regimen: ABVD (Adriamycin, bleomycin, vinblastine, dacarbazine).
Advanced Stage (III and IV, often with bulky disease):
Combination chemotherapy with radiation therapy in select cases.
Chemotherapy Regimens:
ABVD
BEACOPP (bleomycin, etoposide, Adriamycin, cyclophosphamide, oncovin, procarbazine, prednisone).
Additional Options: Anti-CD30 antibodies and autologous stem cell transplantation.