medgems Flashcards

1
Q

thrombocytopenia
otherwise all normal in elderly women

A

immune thrombocytopenic purpura

> Destruction of platelets
autoimmune

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2
Q

how to manage ITP?

A

steroids /IVIG

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3
Q

diamond blackfan anaemia - blood count finding

A

anaemia
low reticulocyte
elevated foetal haemoglobin

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4
Q

poikilocytotic erythrocytes in blood film with patient with myelofibrosis

A

dacrocyte

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5
Q

pre treat chemo pts with?
to prevent?

A

IV allopurinol /rasburicase

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6
Q

reversible agent for dabigtran?

A

Idarucizumab

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7
Q

AML - buzz words

A

auer rods
blast
hepatomegaly

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8
Q

AML subtype M3 management?

A

all trans retinoic acid

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9
Q

all myeloproliferative syndromes can turn into?

A

acute myeloid leukaemia

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10
Q

BCL2 inhibitor - lymphocyte apoptosis in CLL?

A

venetoclax

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11
Q

cofactor in synthesis of protien C, S?

A

vitamin K

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12
Q

Rare. 3x large than erythrocytes. Deep blue (basic) granules. Bilobed nucleus

A

basophil

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13
Q

follicular lymphoma chromosomal translocation?

A

t(14:18)

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14
Q

treatment for cancer that is t(9;22) BCR-ABL

A

imatinib
CML

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15
Q

t911;14)

A

mantle cell lymphoma

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16
Q

how does heparin work?

if severe bleed occurs is there antidote?

A

increasing the action of antithrombin III

protamine sulfate

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17
Q

coeliac blood test?

A

anti tissue transglutaminase antibodiesw

18
Q

what does warfarin inhibit?

A

vit K epoxide reductase

19
Q

molecule secreted by liver inhibits iron absorption?

20
Q

where are auer rods found?

A

inside neutrophils
acute myeloid leukaemia

21
Q

sickle cell disease
glutamate substituted for?

A

valine
position 6 of beta chain
hbS

22
Q

PV rubra vera management?

A

phlebotomy
hydroxycarbamide

23
Q

what oncogene in burkitts

24
Q

most common cause of b12 deficiency?

A

pernicious anaemia

25
clusters of nuclear DNA within erythrocytes?
howell-jolly bodies
26
how to raise plateelt count?
IVIG
27
unfractionated heparin
(requires APTT monitoring)
28
low platelet count how to manage?
Prenisolone
29
heel prick test
Guthrie
30
sickle cell pts what abx prophylaxis? to protect against?
penicillin encapsualted - NHS
31
warfarin reversal agent?
prothrombin complex concentrate
32
Haemoglobin H disease
three defective alpha globin genes. Leads to chronic haemolytic anaemia - with associated splenomegaly
33
beta thalassaemia
reduced, or absent, synthesis of the beta globin chain of haemoglobin
34
Give an example of a treatment which increases fetal haemoglobin synthesis and hence can be used to reduce the severity of sickle cell disease or beta thalassaemia
Hydroxycarbamide
35
alternative forms of haemoglobin that don;t use beta chjain?
HbA2 or Hb
36
warfarin reversal agent?
Phytomenadione vit k1
37
sickle cell is abnormal?
beta globin chain
38
inherited conditions that typically affect the synthesis of the globin chain in the haemoglobin protein
thalassaemia
39
what coagulation factor decreases when starting warfarin
protein c and protein s
40