Crystal Arthropathies Flashcards

1
Q

what are crystal arthropathies characterised by?

A

deposition of mineralised material within joints and peri-articular tissue

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2
Q

name common crystal arthropathies and their crystals

A

monosodium urate - gout
calcium pyrophosphate dihydrate - pseudogout
basic calcium phosphate hydroxy-apatite - calcific periarthritis/tendonitis

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3
Q

what is a TOPHUS/TOPHI

A

massive accumulations of uric acid

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4
Q

with a diagram describe purine metabolism

A

see notes

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5
Q

causes of hyperuricaemia: overproduction

A
malignancy e.g. lymphoproliferative, tumour lysis syndrome
severe exfoliative psoriasis
drugs e.g. ethanol, cytotoxic drugs
inborn errors of metabolism
HGRPT deficiency
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6
Q

causes of hyperuricaemia: under excretion

A
renal impairment
hypertension
hypothyroidism
drugs e.g. alcohol, low dose aspirin, diuretics, cyclosporin
exercise, starvation, dehtdration
lead poisoning
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7
Q

describe Lesch Nyan syndrome

A
HGPRT deficiency
X-linked recessive
intellectual disability
aggressive and impulsive behaviour
self mutilation
gout
renal disease
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8
Q

management of gout: acute flare

A

NSAIDs
colchicine
steroids IA, IM, oral

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9
Q

management of gout: hyperuricaemia

A

does it need to be treated?
1st attack not treated unless: single attack of polyarticular gout, tophaceous gout, urate calculi, renal insufficiency
treat 2nd attack if within 1 yr
prophylactically prior to treating certain malignancies
do not treat if asymptomatic

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10
Q

how can you lower uric acid?

A
  • Xanthine oxidase inhibitor e.g. Allopurinol
  • Febuxostat
  • Uricosuric agents e.g. sulphinpyrazone, probenecid, benzbromarone
  • Canakinumab
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11
Q

what are the rules for loweringuric acid levels?

A

Wait until the acute attack has settled before attempting to reduce the urate level
Use prophylactic NSAIDs or low dose colchicine/steroids until urate level normal
Adjust allopurinol dose according to renal function

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12
Q

who gets pseudogout?

A

elderly females

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13
Q

cauases of pseudogout

A

idiopathic
familial
metabolic

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14
Q

triggers of pseudogout

A

trauma

intercurrent illness

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15
Q

management of pseudogout

A

NSAIDs
IA steroids
no prophylactic therapies

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16
Q

cycle of polymyalgia rheumatica

A

polymyalgia rheumatica –> giant cell arteritis –> high ESR anaemia
20% with PMR have GCA
50% with GCA have PMR

17
Q

what is polymyalgia rheumatica

A

sudden onset of shoulder +/- pelvic girdle stiffness

18
Q

polymyalgia rheumatica age

A

Rare <50

usuaally > 70

19
Q

polymyalgia rheumatica M:F

A

1:2

20
Q

polymyalgia rheumatica ESR

A

usually > 45 often 100

21
Q

polymyalgia rheumatica symptoms

A
malaise
weight loss
fever
depression
arthralgia
synovitis
22
Q

polymyalgia rheumatica diaagnosis

A
compatible Hx
Age >50
ESR >50
dramatic steroid response
no specific diagnostic test
23
Q

polymyalgia rheumatica DDx

A
• Myalgic onset Inflammatory joint disease
• Underlying malignancy
– e.g Multiple myeloma, lung cancer
• Inflammatory muscle disease
• Hypo/ hyperthyroidism
• Bilateral shoulder capsulitis
• Fibromyalgia
24
Q

treatment of polymyalgia rheumatica

A

prednisolone 15mg daily initially
18-24 month course
bone prophylaxis