Lymphoma Flashcards
(32 cards)
Histological Features of Hodgkin Lymphoma (HL)
Reed-Sternberg cells (RS cells)
HL positive for ……… , but often negative for standard B-cell markers (CD19, CD20, CD21, CD22).
CD15+ and CD30+
Clinical Features of HL :
Most commonly presents as lymphadenopathy :
o Neck (cervical, supraclavicular nodes) most common.
o Non-tender, firm, rubbery nodes.
o May present as an anterior mediastinal mass.
Predictable spread for HL
from one lymph node group to the next.
Key diagnostic test: for HL
Lymph node biopsy.
o Presence of Reed-Sternberg cells confirms HL.
Risk factors for HL
o Epstein-Barr virus (EBV) infection.
o Immunosuppression (HIV, transplant).
o Autoimmune diseases (RA, SLE).
WHO Classification of HL
Classical Hodgkin Lymphoma (cHL)
Nodular Lymphocyte-Predominant HL (NLPHL) (rare).
Classical Hodgkin Lymphoma (cHL)
o Nodular Sclerosing HL (most common, 60-80%).
o Mixed Cellularity HL (inflammatory infiltrate).
o Lymphocyte-Rich HL (excellent prognosis).
o Lymphocyte-Depleted HL (poor prognosis).
Staging via PET/CT scan (Lugano classification) for HL
- Stage I: Single node or group.
- Stage II: Multiple nodes on one side of the diaphragm.
- Stage III: Nodes on both sides of the diaphragm.
- Stage IV: Extranodal disease (e.g., liver, bone marrow).
Treatment:of HL
o Chemotherapy + radiation.
o Common regimen (ABVD):
Adriamycin (Doxorubicin).
Bleomycin.
Vinblastine.
Dacarbazine
Classification of NHL
- Based on Cell Type:
o B-cell NHL (most common).
o T-cell NHL. - Based on Growth Pattern:
o Aggressive (rapid growth, B symptoms).
o Indolent (slow-growing, waxing/waning course).
Most common NHL.
Diffuse Large B-Cell Lymphoma (DLBCL
CD19+, CD20+
Diffuse Large B-Cell Lymphoma
Diffuse Large B-Cell Lymphoma treatment
rituximab (anti-CD20 antibody).
t(14;18) translocation → BCL2 overexpression.
Follicular Lymphoma:
Can transform into DLBCL (poor prognosis)
Follicular Lymphoma
t(11;14) translocation → Cyclin D1 overexpression.
Mantle Cell Lymphoma:
Poor prognosis (median survival: 3-4 years).
Mantle Cell Lymphoma
Associated with chronic inflammation
Marginal Zone Lymphoma (MZL)
Marginal Zone Lymphoma (MZL)
o Associated with chronic inflammation
Include
MALToma (H. pylori infection → stomach lymphoma).
Sjogren’s syndrome (salivary gland lymphoma).
Hashimoto’s thyroiditis (thyroid lymphoma).
Highly aggressive B-cell malignancy.
Burkitt Lymphoma
t(8;14) translocation → c-myc activation
Burkitt Lymphoma
“Starry sky” histology.
Burkitt Lymphoma
Strongly linked to Epstein-Barr virus (EBV).
Burkitt Lymphoma: