MEH haematology Flashcards

1
Q

EPO

A

kidney, RBC production

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2
Q

Thrombopoietin

A

liver and kidney, plateler production

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3
Q

spleen made up of

A

red pulp (macrophages)
white pulp (lymphoid follicles)

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4
Q

Spleen functions

A

sequestration and phagocytosis, pooling, extra medullary haematopoiesis, Immunity

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5
Q

Howell Jolly

A

DNA remnants

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6
Q

Splenic sepsis

A

from encapsulated bacteria in hyposplenism, strep progenies, haemophilias influenza, meningococcus

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7
Q

Spectrin

A

actin crosslink

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8
Q

Ankyrin

A

Proteins to cytoskeleton

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9
Q

band 3

A

Chloride and bicarbonate exchange

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10
Q

Protein 4.2

A

ATP binding

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11
Q

Hereditary spherocytosis

A

ankyrin mutation/spectrin

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12
Q

Sepsis and viruses lead to

A

neutropenia

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13
Q

Haemorrhage leads to

A

neutrophilia

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14
Q

Neutrophil =

A

granulocyte

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15
Q

Fhb goes to

A

adult Hb at 3-6 months

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16
Q

Anisocytosis

A

size variation

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17
Q

MCV

A

size of RBC

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18
Q

Thalassemia

A

mutation in globin, decreased MCV

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19
Q

RDW

A

red cell distribution width

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20
Q

G6PDH deficiency can cause

A

Heinz bodies

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21
Q

Pyruvate kinase deficiency can cause

22
Q

Microcytic anaemias =

23
Q

B12 binds to

A

haptocorrin, pernicious anaemia = B12 deficiency

24
Q

Coombs test measures

A

antibodies on RBC

25
MAHA =
haemoglobinaemia (Hb in blood due to breakdown)
26
B12 features
animal origin, stores last 3-6 years
27
Anaemia
Hb lower than normal
28
TAILS
T (alpha or beta) reduced global chain synthesis Ails is reduced haem synthesis
29
Absorption of iron
reductase, DMT1, Ferroportin into blood, Transferrin transports iron around body
30
Hepcidin
produced by liver, inhibits ferroportin
31
Iron deposited in organs as
haemosiderin
32
HFE protein
lowers transferrin and increases hepcidin (not in hereditary haemochromatosis)
33
Fenton reaction causes
hydroxyl radicals
34
Extramedullary haematopoises in B and Alpha thalassaemia leads to
skeletal abnormalities
35
Eliptocytosis
spectrin
36
Treatment for hereditary spherocytosis
splenectomy
37
MPN
essential thrombocythaemia (XS platelets)
38
Polycythamia vera
XS HBC/Hb
39
myelofibrosis
XS hardening of bone marrow
40
JAK2 gene
tyrosine kinase
41
Primary and secondary haemopotises
primary = bone marrow secondary = increase EPO
42
Hydroxycarbamide inhibits
DNA synthesis
43
What is Imatinib
tyrosine kinase inhibitor
44
Renal cell carcinoma can increase EPO and cause
secondary polycythaemia
45
Megakaryocytes produce
platelets
46
Cytokines lead to
iron dysregulation, marrow decreased EPO response, reduced life span of RBCs
47
Prior to EPO therapy, ensure
adequate iron, Vit B12, folate
48
Felty's syndrome
RA, splenomegaly, neutropenia
49
DIC =
bruising, low platelet, increased clot time, increased D dimers
50
Liver disease
Thrombocytopenia (splenic pooling)
51
RBCs in anaemia of chronic disease
often normochromic and normocytic