WBC Markers Flashcards

1
Q

Acute Myelogenous Leukemia

A

Auer Rods; CD13, CD33, CD11b

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2
Q

Acute Promyelogenous Leukemia

A

t(15;17); DIC, Gout, DVT.

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3
Q

Myelodysplastic Syndrome

A

Erythroblasts, Myeloblasts, Megakaryocytes

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4
Q

Acute Lymphocytic Leukemia

A

Intracellular TdT & CD22

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5
Q

Hairy Cell Leukemia

A

Dry Tap; BRAF mutation; TRAP, CD19, CD20. Usually seen in older males, presents with pancytopenia

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6
Q

Hodgkin’s Lymphoma

A

Reed-Sternberg Cells; CD15, CD30

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7
Q

Ann-Arbor Staging: Class I

A

Involvement of single lymph node region or single extralymphatic site/organ

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8
Q

Ann-Arbor Staging: Class II

A

Involvement of 2 or more lymph node regions on the same side of diaphragm

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9
Q

Ann-Arbor Staging: Class III

A

Involvement of lymph node regions on both sides of the diaphragm with or without local invasion of extralymphatic sites

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10
Q

Ann-Arbor Staging: Class IV

A

Diffuse involvement of one or more extralymphatic organs with or without lymph node involvements

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11
Q

MALToma

A

CD19, CD20; Marginal Zone –> Memory B-Cell

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12
Q

Follicular Lymphoma

A

t(14;18), Bcl-2 mutation; centrocytes and centroblasts

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13
Q

Chronic Lymphocytic Leukemia

A

Smudge cells; CD19, CD20, CD23, CD5; spherocytes due to autoimmune hemolytic anemia, hepatosplenomegaly

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14
Q

Warm Agglutinins

A

SLE, CLL

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15
Q

Cold Agglutinins

A

TB, Mycoplasma, Mono

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16
Q

Burkitt’s Lymphoma

A

t(8;14); due to EBV; starry sky, macrophages, with Ki67. Develop Anemia of Chronic Disease

17
Q

Multiple Myeloma

A

Punched-out lytic lesions, Russel Bodies (intracellular cytoplasmic Mott cells), kappa-light chain, IgG, Rouleaux formation, “M-spike”; CRAB

18
Q

Waldenstorm’s

A

Macroglobinemia (IgM); associated with DVT and blindness

19
Q

Adult T-Cell Leukemia

A

HTLV-1; problem with TAX gene which inhibits p53; flower cells.

20
Q

Mycoides Fungiodes

A

Sezary cells with cerebriform nuclei; CD3, CD4; SKIN INVOLVEMENT

21
Q

Leukemoid Rxn

A

WBC count greater than 50,000; LAP (+)

22
Q

Secondary Polycythemia

A

Increased EPO, Increased Hct due to high altitude and RCC

23
Q

Essential Thrombocytopenia

A

Bone marrow contains increased platelets and megakaryocytes

24
Q

Myelofibrosis

A

JAK 2 mutation; teardrop cells and marrow fibrosis. Leukoerythroblastic reaction, increased AML risk

25
Q

Dysplastic Erythropoeisis

A

Ringed Sideroblast (not diagnostic)

26
Q

Psuedo-Pelger-Heut

A

Can transform to AML; neutrophils, not band form (pushed to one side of nucleus)

27
Q

Langerhan’s Histiocytosis

A

Macrophages in tissue and liver; Bierbeck granules

28
Q

Bernard-Soulier

A

Gp1 on platelet; qualitative, not correctable

29
Q

Risoceitin

A

Amplified adheshion of vWF; BT, and PTT due to Factor VIII

30
Q

Hemophilia

A

Hemarthrosis; affected mother with normal father has 50% chance of passing onto all children (25% chance of passing onto son)

31
Q

Chronic ITP vs Acute ITP

A

IgG for chronic, mother passes along; IgM for acute

32
Q

Uremic Platelet Destruction

A

Increased BT, BUN. NORMAL PLATELETS