Haematology Flashcards

1
Q

Most common cause of osteomyelitis in SCD

A

Salmonella

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2
Q

Most common human platelet antigen in NAIT

A

HPA-1a

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3
Q

Extrinsic Pathway (factors and test)

A

Tissue factor and Factor 7, PT

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4
Q

Intrinsic Pathway (factors and test)

A

Factors 12, 11, 9, 8 (aPTT)

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5
Q

What is FFP usually given for?

A

DIC - all factors effected (extrinsic and intrinsic. Preferred option over cryoprecipitate)

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6
Q

What is the most sensitive test for Vit B12 deficiency?

A

Elevated serum (or urine) MMA (methylmalonic acid)

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7
Q

Cryoprecipitate is indicated for replacement of:

A

Fibrinogen. Cryoprecipitate is FFP that has been centrifuged and contains F8, fibrinogen, fibronectin and F13 (in greater concentrations than those in plasma)

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8
Q

Prolonged aPTT which normalises with mixing study is most likely a diagnosis of?

A

Haemophilia

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9
Q

Bone marrow failure, oral leukoplakia and a lacy appearance to skin

A

Dyskeratosis congenita

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10
Q

What is the mechanism of hydroxyurea

A

Increases HbF production

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11
Q

Reed-Sternberg Cells

A

Hodgkin Lymphoma

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12
Q

Auer Rods

A

AML

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13
Q

Spherocytes and DAT neg

A

Hereditary Spherocytosis

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14
Q

Spherocytes and DAT positive

A

AIMA

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15
Q

What is the genetic mutation causing SCD?

A

Missense mutation on the surface os Hb S molecule in the beta globin chain. This mutation results in a substitution of valine (in) for glutamic acid (out) i.e. GTG to GAG.

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16
Q

Bite cells, Blister cells and Heinz Bodies

17
Q

Tear drop cell

A

Vit B12 def

18
Q

Elliptocyte/Pencil cell

19
Q

What is Haemophilia C and how is it inherited?

A

Factor 11 def. Autosomal recessive inheritance

20
Q

What is the reason for a high serum homocysteine but normal serum MMA?

A

Folate def (they would both be raised in Vit B12 def)

21
Q

Microcytic, hypochromic + target cells

A

Thalassemia

22
Q

Normocytic, normochromic + spherocytes

23
Q

Macrocytic, normochromic + ovalcytes

A

Megaloblastic anaemia