Hodgkin Lymphoma Flashcards
Cell of origin of LP cells
germinal center B cells
Clinical of NLPHL
75% are male, age 25-50
5% of all Hodgkin lymphoma
Few show B symptoms
Morphology of NLPHL
- vague large nodules with “moth-eaten” appearance
- cannot be completely diffuse, requires at least focal modularity
- majority of cells in the nodules are benign B cells
- mixed inflammatory cells (eos, plasmas) are rare
- association with PTGC
- ddx: T cell histiocyte rich large b cell
Immunophenotype of LP cells
-B cell markers
-BCL6
-CD45
-EMA in 50%
-ring of CD57, PD1 T cells
Negative for: CD15, CD30 (<5% cases may), EBV
Prognosis of NLPHL
- Indolent, responsive to tx, with frequent local recurrence
- stage I-II>80% 10 year overall survival
- ~5% transform to DLBCL
Treatment of NLPHL
- stage IA: involved field radiation therapy (IFRT) 30 Gy
- all other stages: 2 cycles ABVD + IFRT 20 Gy
Cell of origin of RS/Hodgkin cells
- germinal center B cells with lost B cell phenotype (down regulation of B cell specific transcription factors)
- exhibit over expression of a variety of cytokines/chemokines that result in abundant reactive inflammatory cells seen in classical HL
Classical Hodgkin Lymphoma Clinical
- 95% of all Hodgkin lymphoma
- all except NS show male predominance
- bimodal age 15-40 and late in life
- 40% have B symptoms
Ann Arbor staging
Stage I: single lymph node region or localized involvement of single extra lymphatic organ or site (A: no B sx, B: B sx)
Stage II: 2 or more lymph node regions on same side of diaphragm or localized involvement of single assd extra lymphatic organ or site and its regional lymph nodes with/without involvement of other lymph node regions on same side of diaphragm
Stage III: involvement of lymph node regions on both sides of the diaphragm +/- localized involvement of an associated extra lymphatic organ or site, spleen, or both
Stage IV: disseminated involvement of one or more extra lymphatic organs with/without associated lymph node involvement or isolated extra lymphatic organ involvement with distant nodal involvement
Morphology classical Hodgkin lymphoma
H/RS cells greatly outnumbered by background of non-neoplastic T cells and variable number of mixed inflammatory cells
Immunophenotype of classical Hodgkin lymphoma
positive: CD30, CD15, PAX-5 (dimmer than background B cells), fascia (strong cytoplasmic staining), MUM1
negative: CD45, CD20 (30% of cases weakly pos), Oct2, Bob1
flow may show increased CD4:CD8
Prognosis of classical Hodgkin
pathologic stage and the presence of B sx have greater prognostic value than histologic subtype
Chemotherapy regimens for classical Hodgkin lymphoma
ABVD (most common)