Hodgkin Lymphoma Flashcards
subtypes of classical hodgkin lymphoma
1) nodular sclerosis
2) mixed cellularity
3) lymphocyte rich
4) lymphocyte depleted
demographics of HL
bimodal (first peak around 20, second around 65)
how staging generally work
lymph node distribution
typical presentation
- asymptomatic LAD OR incidental mediastinal mass picked up on CXR (which can cause chest discomfort or respiratory symptoms if large)
- LAD, fatigue, and/or pruritus often recognized to have begun weeks to months before patient is evaluated for cHL
- b symptoms in 40% of patients
pattern of disease involvement? How common is marrow involvement?
- cervical nodes most commonly affected followed by mediastinal nodes
- spread to adjacent lymph nodes
- marrow involvement rare
cell of origin
B-cell lymphoma
staging workup
CT and ***PET/CT
diagnosis of HL
Excisional lymph node biopsy w/ Reed-Sternberg cells
prognosis
Survival rates = Good. Cure obtained in 80% of all patients. 5-year survival of >90% in early, and 75% in advanced-stage disease.
Hodgkin lymphoma is a highly curable disease.
treatment in general and regimen for limited stage
ABVD chemo followed by XRT
ABVD regimen
doxorubicin/bleomycin/vinblastine/dacarbazine
Standard of care for relapsed/refractory HL
high-dose chemotherapy (ICE) followed by autologous HSCT w/ brentuximab consolidation
Definition of bulky disease
Tumors in the chest that are at least ⅓ as wide as the chest, or tumors in other areas that are at least 10 centimeters (about 4 inches) across
Clinical course
Generally slow progression but tempo is variable
2 major subtypes of HL
- Classic HL
- Nodular lymphocyte predominant HL
Lymph node appearance in patients with cHL
- nontender, firm, rubbery
How is weight loss defined as a b symptom
Unexplained loss of greater than 10% of body weight over 6 months
Fever features in Hodgkin’s
- more noticeable in the evening
- gradually becomes more severe and continuous with time
less common presentations of hodgkin’s
- alcohol-associated pain (uncommon but highly specific for HL)
- liver disease
- skin lesions
- bone involvement
laboratory presentation of HL
- hypercalcemia (increased cailcitriol production)
- anemia (multifactorial)
- eosinophilia