Use LEFT and RIGHT arrow keys to navigate between flashcards;
Use UP and DOWN arrow keys to flip the card;
H to show hint;
A reads text to speech;
47 Cards in this Set
- Front
- Back
what part of the LN are the B cells in
|
germinal follicles
|
|
what part of the LN are the T cells in
|
paracortex
|
|
when do you see generalized painless lymphadenopathy
|
seen in systemic disease
ex: SLE, infectionus mono |
|
when do you see localized painless lymphadenopathy
|
malignancy- nodes draining primary cancer sides (breast-> axillary nodes)
Hodgkins Lymphoma (usually 1 cervical and 1 mediastinal) |
|
painless generalized lymphadenopaty
|
malignacy, systemic: Metastasis of leukemia (think CLL) or follicular B cell Lymphoma (indolent in nature)
|
|
malignancy involving cervical LN
|
Hodgkins, Metastatic head tumors (larynx, thyroid, nasopharynx)
|
|
L sided supra-clavicular LN malignancies
|
(virchow's nodes)
metastatic abdominal cancers |
|
R sided supra-clavicular LN malignancies
|
metastatic lung and esphageal cancers, Hodgkins
|
|
Axillary LN malignancies
|
Breas cancer
|
|
Hilar LN Maligancies
|
metastatic lung cancer
|
|
Mediastinal LN malignancies
|
metastatic lung cancer, Hodgkins, T cell lymphoblastic lymphoma
|
|
para aortic LN malignancies
|
metastatic testicular cancer, Burkitt's Lymphoma
|
|
Inguinal Malignancies
|
Metastatic vulvar and penis cancers
|
|
cell type of NH Lymphoma
|
85% B-cell origin- derive from germinal follicle.
|
|
Lymphoma associated with EBV
|
Burkitt's Lymphoma (Aggressive)
|
|
what is the translocation in follicular lymphoma?
|
t(14:18)- results in overexpresion of BCL2 (an anti-apoptotic gene)
|
|
nodal involvement in nodular sclerosing Hodgkin's Lymphoma
|
anterior mediastinal + cervical or supraclavicular
|
|
neoplastic cell of Hodgkin's Lymphoma and cellular markers
|
CD15 and CD30 are present on Reed Sternberg cells
|
|
diagnosis of Hodgkins Lymphoma
|
RS cells with a background of reactive cells (eosinophills, plasma cells, histiocytes)
|
|
differences in distribution of NH Lymphoma and Hodgkins
|
Hodgkins has localized LN involvement while NHL has generalized LN involvement
|
|
clinical "B" signs of hodgkins dz and other clinical sign
|
fever, weight loss >10%, night sweats
non B sign: puritis |
|
type of anemia in Hodgkins Lymphoma
|
Normocytic anemia
|
|
typical staging for Hodgkins Lymphoma
|
I or II: usually stays above diaphragm
I- one site (mediastinal or cervical) II- 2 sites |
|
malignant complications in treatment of Hodgkin's Lymphoma
|
radiation may lead to AML or NHL
|
|
CD1+ cells that contain Birbeck granules
|
Histiocytes
|
|
in what type of Lymph malignancy is skin involvement common?
|
Malignant Histiocytosis (histiocytosis X)
|
|
signs of mast cell disease
|
puritis, swelling, hyperpigmentation
|
|
define Bence Jones protein
|
Ig light chains in urine
|
|
what age is multiple myeloma seen in?
|
elderly- rarely seen under 40
|
|
what protein spike is seen in Multiple Myeloma
|
M-spike
Usually IgG kappa followed by IgA |
|
bone marrow findings in multiple myeloma
|
plasma cells > 10 % of cells
|
|
bone findings in multiple myeloma
|
lytic lesions (punched out), pathologic fractures, hypercalcemia
|
|
multiple myeloma "crab"
|
hyperCalcemia
Renal failure Anemia Bone destruction/pain |
|
2 ways kidneys are damaged in multiple myeloma
|
acutely from hypercalcemia
tubular epithelium is damaged by BJ proteins |
|
smear findings in multiple myeloma
|
rouleauz formations
|
|
most common cause of death in multiple myeloma
|
recurrent infections
|
|
MUGS
|
asymptmatic IgG M spike
plasma cells in bone marrow < 3% no BJ proteins or CRAB symptoms |
|
epidemiology of Waldenstrom's macroglobulinemia
|
elderly, male-dominant disease
|
|
Waldenstrom's Triad
|
result of hyperviscocity from increased IgM
1. Bleeding (platlet ag defects) 2. Visual changes (retinal hem) 3. Neurologic changes (stroke) |
|
what cell cause Waldenstrom's macroglob?
|
neoplastic lymphoplasmocytoid B cells
|
|
LN involvement in Waldenstrom's vs Multiple Myeloma
|
generalized Lymphadenopathy in Wald. not present in MM
|
|
most common monoclonal gammopathy
|
MUGS
|
|
evidence of splenic dysfunction on peripheral smear
|
howell-jolly bodies (nuclear remnants)
|
|
infection risk increases with splenectomy; why?
|
concentration of IgM and C3b drops leading to
decrease in complement activation (IgM) decreased opsonization (C3b) |
|
Pathogens patients susceptible to with splenectomy
|
Hflu, strep, Salmonella
|
|
most common cause of splenomegaly in developing countries?
|
malaria
|
|
BJ renal disease
|
proteinaceous casts with multinucleated giant cell reaction
|