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40 Cards in this Set

  • Front
  • Back
JAK2 mutation
Mutation in PV, ET, MMM
t(15;17)
Translocation in M3/promyelocytic AML
t(9;22)
Translocation in CML
CD10+ (CALLA+), tDt+
B-ALL marker
CD20dim+, CD23+, CD5+, CD19+
CLL marker
CD103+, CD25+ CD11c+
Hairy Cell Leukemia marker
Stains TRAP+
Hair Cell Leukemia stain
CD4+, tDt-
Adult T-Cell Leukemia/Lymphoma marker
CD10+, tDt+, CD24+ CD19+, CD79+
B-lymphoblastic L/L (immature) marker
CD3+, CD5+, tDT+
T-Lymphoblastic L/L (immature) markers
CD10+, CD20+, CD5-, CD3-
Follicular Lymphoma marker
BCL2 overexpression
Follicular Lymphoma over expresses this
t(14,18)
Translocation in Follicular Lymphoma
CD20bright+, CD5+, CD23-, cyclinD1+, lambda+
Mantle Cell Lymphoma marker
t(11,14)
Translocation in Mantle Cell Lymphoma
t(8;14), c-myc oncogene
Translocation in Burkitt's Lymphoma
Ki-67 = 100%
Burkitt's Lymphoma expresses this
CD3+, CD7-, CD26-, CD4+
Mycosis Fungoides (sezary syndrome) marker
CD15+, CD30+, CD45-
Hodgkins Lymphoma marker (classical)
CD15-, CD30-, CD45+
CD20+, CD57+
Nodular Lymphocyte Predominant HL (NLPHL)
(aka "NON-CLASSICAL" HL)
S100+, CD1a+, CD207
Langerhans Cell Histiocytosis marker
tennis racket shaped (birbeck granules)
Langerhans Cell Histiocytosis marker
Signs of GOOD prognosis in AML
t(8;21)inv(16)
Signs of GOOD prognosis in ALL
t(12;21)= TEL-AML1
1-10yo
WBC<50,000
hyperdiploidy
Signs of POOR prognosis in ALL
philadelphia chromosome
MLL/11q23
hypodiploidy
Signs of POOR prognosis in CLL
zap70 (pre-GC, unmutated Ig)
CD38+
Trisomy 12
Age Group: ALL
0-14yo
Age Group: AML
15-60yo
Age Group: CML
40-60+ yo
Age Group: CLL
>60yo
7 factors of the Hodgkin Disease International Prognostic Score
Age>45; Male; Stage 4;
alb<4; Hb<10.5; WBC>15k; lymphopenia
Variant of HL with:
many lymphocytes & few RS
Lymphocyte predominant HL
Variant of HL with:
fibrous bands, lacunar cells, F>M
Nodular Sclerosis HL
Variant of HL with:
eosinophils, plasma cells, fibrosis, setting of HIV, EBV-assoc, lower SES
Mixed Cellularity HL
Variant of HL with:
few lymphocytes, many RS cells, necrosis, aggressive w/ B-Sx
Lymphocyte-Depletion HL
Variant of HL with:
noB-Sx, no RS, peripher LAD,
L&H "popcorn" cells; good prognosis
Nodular Lymphocyte Predeominant HL (NLPHL)
aka: "non-classical HL"
DiGeorge Syndrome defect
chrom 22q11.2
Failure of 3rd and 4th pharyngeal pouches to develop (no thymic envelope)
T-B+
Wiskott Aldrich syndrome Triad
eczema
thrombocytopenia
immunodeficiency syndrome (SP infxns)
Hand-Schuller Christian Sx
Diabetes Insipidus
Skull lesions
exophthalmos
Letterer-Siwe Dz Sx
LAD, Skin lesions, Diarrhea

pancytopenia, failure to thrive, osteolytic bone lesions, pulmonary lesions