Approach to the Cytopaenic Patient Flashcards

1
Q

What are the causes of impaired blood cell production?

A

acquired aplastic anaemia
congenital aplastic anaemia
bone marrow infiltrative disorders
myelodysplastic syndrome

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2
Q

What is the cause of acquired aplastic anaemia?

A

autoimmune destruction of pluripotent haematopoietic stem cells by T lymphocytes

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3
Q

What are the findings of a bone marrow biopsy in asquired aplastic anaemia?

A

reduced cellularity

absence of fibrosis and malignant cells

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4
Q

What is the treatment for idiopathic acquired aplastic anaemia?

A

if less than 50 -> HSCT

if > 50 -> triple immunosuppressive therapy: anti thymocyte globulin, cyclosporin, methylprednisolone

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5
Q

What drugs can cause pancytopaenia?

A
benzene
chemotherapy drugs
NSAIDs
anti epilpetics
steroids
chloramphenicol
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6
Q

Why should patients be tested for dihydropyrimidine dehhydrogenase deficiency prior to starting fluropyrimidines?

A

increased risk of severe/fatal pancytopaenia

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7
Q

What is the mechanism in which alcohol causes pancytopaenia?

A

direct bone marrow toxicity
increased iron absorption -> iron overload and cirrhosis
interference with folate absorption
acetaldehyde forming adducts with cell membrane phospholipids -> damages red blood cells

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8
Q

When is the nadir of pancytopaenia with radiotherapy?

A

1-4 weeks

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9
Q

What are the common viral causes of pancytopaenia?

A
hepatitis A, B, C
CMV
EBV
HHV6
HIV
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10
Q

What are the main solid tumours which can cause bone marrow infiltrative disorders?

A

prostate, breast, lung

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11
Q

What are causes of peripheral destruction leading to pancytopaenia?

A

autoimmune mediated

splenic sequestration

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12
Q

What mutation causes paroxysmal nocturnal haemoglobinuria?

A

mutation in PIGA gene

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