heme onc Flashcards

1
Q

neutrophilic state after corticosteroids (or increased cortisol during cushings)

A

increased apparent neutrophils due to release from marginated pool

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2
Q

when theres a left shift, i.e. during infection, what marker is decreased

A

cd16 (binds Fc of IgG)

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3
Q

hemaopoietic stem cell marker

A

cd34

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4
Q

whats the cell state in digeorge

A

no thymus = no t cells = leukopenia

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5
Q

basophilia

A

CML

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6
Q

leukocytosis vs lymphocytosis

A

increase in wbc–> seen in infection

lymphocytosis –> increase in lymphocytes, i.e CD8 cells for viral infection

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7
Q

the one bacteria that can cause lymphocytosis (increased)

A

bordatella pertussis

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8
Q

LN cortex

A

B cells

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9
Q

LN paracortex

A

T cells. i.e. EBV infection this increases

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10
Q

periarterial lymphatic sheet (PALS)

A

white pulp of spleen. around the arteries. this is where t cells are preent. this area will eb expanded during infection i.e. EBV

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11
Q

ALL (LymphoBLASTIC so its a Precursor B/T leukemia): B vs T (can only diff by immunotyping)

(vs AML = MPO +, Auer Rods)

A

all are TdT+ (and PAS +)

Precursor T: CD1, CD2, CD3, CD5, CD8

Precursor B: CD19, CD10

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12
Q

CD5 is a ______ - cell marker, but can also be seen with ________ (a _____ cell neoplasm)

A

CD5 = T-cell marker

however, SLL/CLL = CD20+, CD5+ B cell neoplasm (so expresses B cell marker and co-expresses T cell marker on surface)….smudge cells

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13
Q

point mutations in splice sites and promoter regions

A

Beta thalassemia (decreased beta-globin production)

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14
Q

Severe anemia requiring frequent blood transfusions in ___ - ______ leads to _____________

A

beta-thalassemia

leads to HEMOCHROMATOSIS–>need iron chelation therapy to reduce load

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15
Q

What happens to marrow in beta thalassemia

A

Since you have anemia, get

  • marrow expansion (crew cut skull, chipmunk facies)
  • extramedullary hematopoiesis (hepatosplenomegaly) = increase risk Parvo B19 induced APLASTIC CRISIS
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