haem I don't know Flashcards

1
Q

Treatment of myelofibrosis

A

only cure is an allogenic stem cell transplant

if symptomatic, give chemotherapy to shrink the spleen and prevent marrow angiogenesis- ruxolitnib or hydroxycarbamide

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2
Q

mechanism of myelofibrosis

A

myeloproliferative disorder- JAK 2 mutation

hyperplasia of megakaryocytes, leading to platelet derived growth factor, stimulating fibroblasts

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3
Q

%myelofibrosis that transforms to leukaemia

A

15%

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4
Q

action aspirin

A

acts on COX 1 preventing thromboxane a2

affects aggregation for full lifespan of platelet

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5
Q

treatment of iron deficiency

A
  1. oral iron suppliment
  2. iv iron
  3. red cell transfusion only if symptomatic at rest
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6
Q

how to measure iron levels in blood

A

serum ferratin

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7
Q

blood film- Iron deficience anaemia

A

microcytosis, hypochromic,

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8
Q

neuro complication of b12 deficiency

A

Subacute combined degeneration of spinal cord, treat with b12 and folate suppliments

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9
Q

names of alpha thatassaemia diseases

A

1 missing- trait
3 missing- HbH disease (low mcv and mch)
4 missing- Hb barts hydrops fetalis

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10
Q

treatment sickle crisis

A

analgesia
antihistamine
hydration
antibiotics

if acute chest- give oxygen and spirometry

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11
Q

sicke cell aplastic crisis

A

cessation of RBC production due to parovirus B19

blood film has no reticulocytes

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12
Q

causes of intravascular haemolysis

A

ABO incompatibility
G6PD
Black water fever

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13
Q

pathophysiology of anaemia of chronic disease

A

increased hepcidin
increased cytokies TNF and IL1 and 6
shortened RBC lifespan
blunted EPO

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14
Q

where does cold and warm haemolysis occur

A

warm- exravascular

cold- intravascular in peripheries

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15
Q

Haemoglobin tyes present in haemoglobin A1

A

a2, b2

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16
Q

Haemoglobin tyes present in haemoglobin A2

A

a2, delta2

17
Q

Haemoglobin tyes present in haemoglobin F

A

a2 and gamma 2

18
Q

HbA1C

A

A2, b2, glucose

19
Q

genetic abnormality in AML

A

oncogenic mutations impeding differentiation

20
Q

Blood count resut in CML

A

Inc wbc
Inc eosin
inc basophil

21
Q

blood film result in AML

A

auer rods

>30% myeloblasts

22
Q

cells present in hodgekins lymphoma

A

reed sternberg cells

23
Q

What is R-CHOP

A

Rituximab

Cyclophosphamide
doxorubicin Hydrochloride
Oncovin (now called vincristine
Prednisolone

24
Q

when is r-chop used

A

treatment of non-hodgekins lymphoma

25
Q

rituximab mechanism of action

A

attacks cd20- present on b cells

26
Q

protein found in myeloma

A

bence jones protein (light chain found in urine)

27
Q

backache and raised ESR

A

myeloma

28
Q

The oxygen-haemoglobin dissociation curve is shifted to the right in which of the following scenarios?

Hypothermia

Respiratory alkalosis

Low altitude

Decreased 2,3-DPG in transfused red cells

Chronic iron deficiency anaemia

A

iron deficiency anaemia

right shifting-

CADET face RIGHT

C O2
A cidosis
2,3-DPG
E xercise
T emperature
29
Q

what is gilbert’s syndrome

A

Gilbert’s syndrome is a genetic disorder that’s hereditary (it runs in families). People with the syndrome have a faulty gene which causes the liver to have problems removing bilirubin from the blood.

30
Q

what is factor 3 also known as

A

tissue factor

31
Q

what is Bernard soulier syndrome

A

Bernard-Soulier syndrome is an autosomal recessive bleeding disorder caused by a deficiency in the platelet glycoprotein complex Ib-IX-V, which would normally bind to von Willebrand factor (vWF) to allow platelet adherence. As vWF cannot bind, platelet adhesion is impaired and patients present with usual symptoms of coagulopathies like abnormal bleeding and bruising.