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50 Cards in this Set

  • Front
  • Back

Mutation in CD 18

Leukocyte Adhesion Deficiency (LAD)



- No intergrins = no tight binding = increased circulating neutro's and no neutro's in inflammed tissue

Mutated NADPH oxidase

Chronic Granulomatous Disease (CGD)



No resp. burst in Neutros -> recurrent bacterial/fungal ifxns

GM-CSF treated Neutro w/ Toxic Granulation



-"May-Hegglin Anomaly" = Dohle Bodies (RER remnant), large granules, vacuoles, L-shift

Toxic Degranulated Neutro due to sepsis



- Same as GM-CSF treated but have bacterial inclusions

Chediak-Higashi Syndrome



- recessive mutation causing abnormal degranulation w/ large aggregated inclusions, pancytopenia, and recurrent pyogenic ifxns

Mutated RAS

Signal-transducer oncogene


- causes no GTP hydrolysis = continual growth signals

Deletion of 17q

Li-Fraumeni Syndrome



- inherit one mutation of p53 (detects DNA damage -> activates p21 to inhibit cycD/CDK4)


* Increased risk of cancer

CD45

WBC

CD34

Stem Cell

CD2-8

T-Cell


(Immature = Neg for 4 & 8, Int = Pos for 4 & 8, Mature = Pos for 4 or 8)

CD19

Immature and Mature B cells

CD 20

Mature B cells

CD38

Plasma Cells

CD16, 56

NK cells

CD 15, 13, 33

Myeloid

CD 61

Megakaryocyte

Glycophorin A

Mature RBC

CD71

Transferrin on RBC

MPO+, SBB+, NSE+


CD117+


CD 13, 33+

Acute Myeloid Leukemia


*CD117 = c-kitt that inhibits apoptosis

MPO-, TdT+

Acute Lymphoid Leukemia/Lymphoma

CD34+, HLA-DR+

Acute Promyelocytic Leukemia


*EMERGENY all-trans retinoic acid administration!

t(17,15) Retionic acid receptor (RAR)

Acute Promyelocytic Leukemia



Blocks maturation causing Faggot Cells w/ Auer Rods to form sheets of cell -> degranulate to cause DIC!

t(8, 21) ETO

AML w/ Neutrophil Maturation



Good prog

Inversion of CBFB and MYH11 genes on Chr 16

AML w/ Monocyte and Granulocyte Matuation



*Abnormal eosinophils in BM



Good prog

t(1, 22) and no MPO expression

Acute Megakaryoblastic Leukemia


*Poor prog, seen in kids/infants -- especially Down's kids < 5

NPM1 mutation

1/3 of AML's -- indicate good prognosis unless that also have FLT3-ITD mutation

TdT+


CD 10, 19, 20+

B-ALL

t(12,21) Hyperdiploid

B-ALL w/ good prognosis


(TEL/AML)

t(9, 22), Hypodiploid


p190

B-ALL w/ poor prognosis



- BCL-R/ABL fusion protiein that increases Tyr kinase activity

TdT+


CD 2-8+


CD10-

T-ALL

t(9, 22)


p210 breakpoint point protein

"Philidelphia Chromosome" - CML



*BCR-ABL fusion protein that increases Tyr kinase activity

JAK2 Kinase mutation

50% Myelofibrosis (rest are CALR mutants),


50%Essential Thrombocythemia,


95% Polycythemia Vera

KITT mutation

Mastocytosis (type of MPN)

5q deletion

Myelodysplastic Syndrome w/ increased plts and macrocytic anemia seen in elderly females

CD45+, CD10+


CD 15-, CD 30-

Non-Classical Hodgekin Lymphoma = Nodular Lymphocyte Predominant



*L & H cells

CD45-, CD10-


CD15+, CD30+

Classical Hodgekin Lymphoma


(Nodular Sclerosis, Mixed Cellularity, Lympho-Predom, Lympho-Depleted)



*Painless supradiagphragmatic LAD, Reed-Sternberg cells

BCL-2+, CD10+

Follicular Lymphoma (Low Grade, Stage IV)

t(14, 18)

BCL-2 to Ig heavy chain


Follicular Lymphoma (Low grade, Stage IV)

t(14, 8)

c-myc to Ig Heavy Chain


Burkitt's Lymphoma (High grade)

"Starry Sky" sheet of cells that are BCL-2 negative

Burkitt's Lymphoma (High Grade)

t(14, 11)

Cyclin D1 to Ig Heavy chain


Mantle Cell Lymphoma

Naive B cells co-expressing CD5+ and CD20+

CLL

t(2, 5)


Horseshoe-nucleus cells +ALK

Anaplastic Large T Cell Lymphoma

Proliferation of clonal light chain memory B cells especially in MALT

Marginal Zone Lymphoma

Pautier Microabcess (CD4+ proliferation in epidermis)

Mycosis Fungoides

Skin CD4+ lymphoma with spread to blood w/ popcorn like cells

Sezary Syndrome in Mycosis Fungoides

CD4+ Proliferation w/ Hepatospleenomegaly, hypercalcemia w/ lytic bone, flower cells

Adult T Cell Leukemia/Lymphoma

+S-100a, CD1a, Langerhan

Langerhan's Cell Histocytosis

Birbeck (tennis Racket) granules and skull lytic leisons

Langerhan's Cell Histocytosis

Many translocations that all result in upregulation of Cyclin D

MGUS, Solitary Plasmacytoma, Multiple Myeloma