other anemias Flashcards

(38 cards)

1
Q

what is a deficiency of EPO associated with ?

A

normocytic anemia

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
2
Q

what is the cause of aplastic anemia ?

A

associated of loss of hematopoeitic precursors kolohom - this results in pancytopenia

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
3
Q

what are the hallmarks associated with aplastic anemia ?

A

associated with pancytopenia
acellular or hypocellular bone marrow

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
4
Q

what is seen on biopsy of aplastic anemia ?

A

absence of cells or replacement with fat cells

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
5
Q

what are the symptoms of aplastic anemia ?

A

pancytopenia
anemia
thrombocytopenia
leukopenia

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
6
Q

what is the inherited cause of aplastic anemia ?

A

fanconis anemia

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
7
Q

what is the mechanism behind idiopathic aplastic anemia ?

A

immune mediated mechanism
t cell mediated destruction of stem cells

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
8
Q

what is the treatment for aplastic anemia ?

A

can be treated with antithymocyte globulin
cyclosporine

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
9
Q

what chemicals are associated with causing aplastic anemia ?

A

benzene

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
10
Q

what drugs are associated with causing aplastic anemia ?

A

chloramphenicol
methimazole and PTU

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
11
Q

what are the viruses associated with causing aplastic anemia ?

A

parvovirus B19
acute viral hepatitis

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
12
Q

what is the presentation associated with fanconis anemia ?

A

inherited aplastic anemia
short stature
cafe au lait spots
malformed thumbs

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
13
Q

what is the mechanism associated with fanconis anemia ?

A

defective DNA repair
genetic loss of DNA crosslink repair; often progresses to AML

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
14
Q

what is the key association of red cell aplasia ?

A

thymoma where there is an absence of erythroid precursors in the bone marrow

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
15
Q

what is the main problem associated with megaloblastic anemia ?

A

red blood cell precursors grow bu they cannot divide , results in abnormal DNA synthesis

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
16
Q

what are the lab findings associated with megaloblastic anemia ?

A

anemia
large RBCs
hypersegmented neutrophils

17
Q

what is the pathology associated with heyes syndrome ?

A

deficiency in the VWF

18
Q

what are the different causes of megaloblastic anemia ?

A

folate deficiency
B12
orotic aciduria
hydroxyurea
phenytoin
sulfa drugs

19
Q

what are the symptoms and findings associated with folate deficiency ?

A

increased homocysteine levels
normal methymalonic acid
no neurological symptoms

20
Q

what are the causes associated with folate deficiency ?

A

chronic alcohol use , malabsorption drugs

21
Q

what are the main causes of vitamin b12 deficiency ?

A

mostly associated with pernicious anemia
malabsorption like with crohns disease

22
Q

what tapeworm is associated with vitamin b12 defeceincy ?

A

diphyllobothrium latum ( fish tapworm)

23
Q

what test is used to differentiate between dietary insufficiency and malabsorption of B12?

A

schilling test

24
Q

how long does anemia secondary to insufficient take of vitamin b12 take ?

A

may take years to develop

25
what is the effect of giving folate in vitamin b12 deficiency ?
will improve the anemia but worsen the neurological symptoms
26
what are the neurological symptoms associated with vitamin b12 deficiency ?
reversible dementia subacute combined degenration
27
what is the problem with orotic aciduria ?
causes megaloblastic anemia due to inability to convert UMP due to defect in UMP synthase
28
what is the presentation of orotic aciduria ?
present in children as failure to thrive , developmental delay and megaloblastic anemia refractory to folate and b12 treatment
29
how can we differentiate between orotic aciduria and ornithine deficiency ?
increased orotic acid levels with no hyperammonemia in orotic aciduria
30
what is non megaloblastic macrocytic anemia ?
macrocytic anemia with normal DNA synthesis , no hypersegmented neutrophils
31
what are the causes associated with nonmegaloblastic anemia ?
chronic alcohol use and liver disease
32
what is a cause of non megaloblastic macrocytic anemia ?
diamond blackfan anemia , a congenital form of red cell aplasia
33
what is the difference between diamond blackfan anemia and fanconis anemia ?
fanconis is associated with pancytopenia whilst the other is due to pure red cell aplasia
34
what is the pathology associated with diamond blackfan anemia ?
happens in the first year of life due to intrinsic defect in erythroid progenitor cells
35
levels of which type of HB is raised in diamond blackfan anemia ?
increased HbF
36
what is the distinctive presentation associated with diamond blackfan anemia ?
tripharyngeal thumb
37
what are the features of anemia of chronic disease ?
everything is low except ferritin
38
what is the actual pathology associated with aplastic anemia ?
failure of destruction of hematopoeitic cells