Last Brown Lecture Flashcards

1
Q

Tx for hereditary spherocytosis

A

Splenectomy

Howle-Jelly bodies (left-over DNA) will be present - spherocytes will still be present

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2
Q

EBv results in what abnormal lymphocytes in the peripheral smear?

A

CD8+ T cells

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3
Q

Howle-Jolle bodies are remnants of?

A

“Left-over” DNA from hemolytic anemia of spherocytosis

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4
Q

With a presentation of infectious mononucleosis, what is the main DDx?

A

Hodgkin lymphoma

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5
Q

What are the main two causes of petechiae

A
  1. Quantitative platelet dysfunction
  2. Vasculitis
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6
Q

Cause of palpable purpura

A

vasculitis

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7
Q

What clotting factor deficiency is indicated by a prolonged PTT and prolonged PT?

A

Factor V deficiency (common pathway)

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8
Q

What causes the finding of shistocytes in the peripheral smear?

A

TTP

DIC

HUS

Micro- or macroangiopathic hemolytic anemia

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9
Q

What are the vitamin-K dependent coagulation factors?

A
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10
Q

How does intravascular hemolytic anemia affect the serum haptoglobin concentration?

A

Haptoglobin decreases (hemoglobin binds)

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10
Q

Why is free hemoglobin toxic?

A

Hb is much larger than albumin, disrupts the osmotic balance

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11
Q

In a sickle-cell Pt w/ an autoinfarcted and nonfunctional spleen, what would you expect to see in the peripheral blood smear?

A

Howell-Jolly bodies

https://pressbooks.openeducationalberta.ca/mlsci/chapter/abnormal-rbc-inclusions-howell-jolly-bodies/
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12
Q

Chronic hemolytic anemias of childhood

A

Sickle-cell disease

Severe beta-thalassemia

Hereditary spherocytosis

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13
Q

What conditions would you see extramedullary hematopoeisis?

A

Space occupying lesion in the marrow:

Malignancies in the bone marrow

Myelofibrosis

Granulomas (non-caseating = TB, caseating = sarcoid)

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14
Q

What causes functional asplenia in Pt’s w/ sickle-cell anemia?

A

Multiple splenic infarcts

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