lymphoid malignancies Flashcards
acute lymphocytic leukemia characteristics
stem cell disorder
malignant proliferation
peak age 2-5 yoa
acute lymphocytic leukemia etiology
idiopathic
chromo ab (Downs syndrome)
leukemogenic factors
acute lymphocytic leukemia clinical course
abrupt onset
fatigue, pallor, weight loss, fever, bruising, bone pain
acute lymphocytic leukemia laboratory presentation
n/n anemia
thrombocytopenia
v wbc
diff: blasts (no auer rods)
cytochemistry: block + PAS
cell markers: CALLA, CD
classification: FAB
bm: hypercellular (increased blasts)
ALL TREATMENT
chemo/ radiation
bm transplant
umbilical cord treatment
80% survival in children
chronic lymphocytic leukemia laboratory presentation
n/n anemia
decreased plts
increased wbc
neutropenia
lymphocytosis
small lymphs
smudge cells
CML treatment
supportive
chemo/ radiation as needed
hairy cell leukemia characteristics
adult disease
male; female= 7:1
hairy cell leukemia clinical presentation
splengomegaly
increased infection
hairy cell leukemia laboratory presentation
pancytopenia
hairy cells
fibrosis in bm
TRAP stain +
immunophenotyping: B cells positive for CD 19, 20, 22, 25 etc.
hairy cell leukemia therapy
supportive
splenectomy
chemo
multiple myeloma charachteristics
adult median age 65
male predominance
malignant proliferation of plasma cells
monoclonal gammopathy (most IgG)
multiple myeloma clinical presentation
bone pain
lytic bone lesions and fractures
symptoms related to abnormalities
multiple myeloma laboratory presentation
increased plasma cells in bm
+/= plasma cells in peripheral blood
increased serium Ca
Bence Jones protein in urine
rouleaux
hazy smear
increased ESR
flame cells
ab. plasma cells with Dutcher bodies
immunophenotyping/ cytogenetics
multiple myeloma therapy
poor prognosis
chemo
bm/ stem cell transplant
death due to infection, fractures, renal failure