Pathology 1 Flashcards

(48 cards)

1
Q

list 4 types of non-neoplastic conditions

A

connective tissue
metabolic disease
fractures
degenerative disease

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2
Q

autoimmune disorders can cause connective tissue disease, true or false?

A

true
inflammatory disease
often present with MSK symptoms and signs but have potential for systemic symptoms

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3
Q

how can autoimmune disorders be diagnosed?

A

auto-antibodies
however in some conditions there are very strong, specific associations with auto-antibodies and disease while others not so much

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4
Q

give 4 autoimmune markers?

A

rheumatoid arthritis - rheumatoid factor
lupus - structural parts of DNA
Scleroderma - anti-centromere, antielomere
dermatomyositis - anti Jo

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5
Q

what is rheumatoid arthritis?

A

inflammation of joints with autoimmune basis
- rheumatoid factor
- auto antibodies against Fc IgG
can be systemic (can occur in absence of joint disease but with manifestations in other places like soft tissue etc)

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6
Q

histology of rheumatoid arthritis?

A

plasma cells

lots of inflammatory cells

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7
Q

what happens in the acute phase of rheumatoid arthritis?

A

pannus formation at edges of articular surfaces and then spreads over - inflammatory granulation tissue
hyperplastic/reactive synovium

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8
Q

what happens in chronic phase?

A

fibrosis
deformity
cartilage is destroyed by inflammatory processes causing loss of joint space

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9
Q

what is SLE?

A

systemic autoimmune condition

autoantibodies directed at parts of DNA

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10
Q

name 2 diagnostic markers of SLE

A

ANA (95%)

anti double stranded DNA (40-60%)

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11
Q

what is often required for diagnosis of inflammatory arthritides?

A

clinic-pathological correlation - clinical features and biopsy

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12
Q

name 3 metabolic diseases

A

pagets
osteomalacia
crystal arthropathies

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13
Q

what is crystal arthropathy?

A

gout - urate crystals in joint space

pseudogout - calcium pyrophosphate crystals in joint space

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14
Q

how does crystal arthropathy occur?

A

uric acid is end product of purine synthesis (adenine and guanine)
so urate is formed in DNA replication etc
either increased production or reduced excretion of urate

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15
Q

what can cause increased production of urate?

A

usually idiopathic
enzyme defect (HGPRT) = lysch Nyhan syndrome (rare)
Increased cell turnover - psoriasis, cancer following chemotherapy (causes tumour lysis)

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16
Q

what is the most common cause of gout?

A

under-excretion

can be a drug side effect (thiazides)

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17
Q

how do urate crystals end up in joints?

A

precipitation of crystals (due to reduced solubility, not necessarily to do with amount)
unclear how they end up in joint

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18
Q

how does urate cause pain?

A

crystals elicit acute inflammatory reaction which can mimic arthritis or infection in joint
can cause secondary degenerative changes

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19
Q

what other 2 sites can urate crystals deposit in?

A

soft tissues - gouty tophus

Kidneys - renal disease (stones)

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20
Q

what are the pathological findings in gout?

A

cytology - cross polarised light used to see needle shaped crystals in joint fluid
histology - amorphous eosinophilic debris and inflammation (giant cells - almost like granuloma reaction), crystals lost during tissue processing

21
Q

which is 100% diagnostic of gout?

A

cytology

histology findings could also be pseudogout

22
Q

what is calcium pyrophosphate?

A

crystal arthropahy - pseudogout/pyrophosphate arthropathy

usually affects large joints in older people

23
Q

how does psuedogout present?

A

usually aymptomatic but can cause pain

crystals are more rhomboid in shape (thicker and bigger than needles in gout)

24
Q

what is pagets disease of bone?

A

abnormality of bone turnover
increased osteoclastic activity
more bone but not normally structured - often weaker so can commonly fracture

25
what can cause pagets disease?
``` uncertain some genetic elements (RANKL) viral infections - measles - RSV - paramyxovirus ```
26
what are the 3 stages of pagets disease?
osteolytic mixed burnt out end result is thick excess bone with abnormal reversal lines - mosaic pattern
27
what are the 5 symptoms of pagets?
can affect all bones pain - microfracture or nerve compression enlargement and abnormal shape increased metabolism - heat, AV shunt (can cause heart failure) secondary malignancy - osteosarcoma
28
osteomalacia?
abnormal vit D metabolism | can cause rickets
29
what are the initial phases of fracture?
haematoma - fibrin mesh influx of inflammatory cells cytokine release - osteoprogenitor cells after week 1 - callus forms - organised haematoma, early recruitment and remodelling at the ends of the bone
30
2-3 weeks after fracture?
maximum girth of callus woven bone deposited perpendicular to cortical bone cartilage deposition at fracture site which undergoes ossification bridging with a bony callus
31
remodelling?
woven bone in callus is constantly remodelled - less stress on area, better remodelling to normal shape
32
why might a fracture be sent to pathology?
abnormal bone before break | break doesn't match level of trauma
33
what can cause a fracture other than trauma?
osteoporosis malignancy tumours ………..
34
what can cause a fracture other than trauma?
osteoporosis malignancy tumours
35
what are myeloma/plasmacytoma?
malignant proliferation of plasma cells | can cause bony lesions
36
osteolytic vs osteosclerotic?
``` osteolytic = tumour breaks down/thins bone osteosclerotic = tumour causes increase in bone density and hardening of bone ```
37
what can cause avascular necrosis?
``` trauma alcohol (large cause) dysbarism steroid injection sickle cell disease infection ```
38
what does avascular necrosis look like?
wedge shaped infarct often sub cortical histology - creeping substitution - new bone growing over dead bone (indicative of healing phase)
39
degenrerative joint disease?
mechanical injury to joints - osteoarthritis | can be secondary to other joint disease
40
what secondary disease can avascular necrosis cause?
osteoarthritis
41
what causes degenerative disease?
mechanical injury to joints - osteoarthritis | can be secondary due to other joint disease
42
what changes occur in joints in degenerative disease?
fibrillation (roughening) cartilage is worn away until surface becomes polished bone on bone - eburnation/erosion synovial fluid leaks through bone forming subchondral cysts remodelling of bone to cope with stress produces outgrowths - osteophytes
43
acute features of inflammatory arthritides?
oedema fibrin reactive features in synovial cells
44
what causes pseudogout?
usually idiopathic | can be due to hypercalcaemia, haemachromatosis, hypomagnesia, ochronis, hypothyroidism
45
loss of joint space on X ray?
cartilage loss
46
subchondral sclerosis on X ray?
eburnation
47
sunchondral cysts on X ray?
synovial fluid accumulation
48
osteophytes on X ray?
disorganised bone remodelling