Sarcoidosis Flashcards

1
Q

what is it

A

multi system granulomatous disorder of unknown cause

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2
Q

epidemiology

A

age 20-40 years, female more, afro Caribbean more

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3
Q

how often is it found incidentally

A

in 20-40% on a CXR

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4
Q

what is the finding on CXR

A

bilateral hilar lymphadenopathy +- pulmonary infiltrates or fibrosis

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5
Q

what are the symptoms in pulmonary disease

A

dry cough, progressive dyspnoea, decr exercise tolerance, chest pain

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6
Q

what are the non pulmonary haem signs

A

lymphadenopathy, hepato spleno megaly,

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7
Q

what are the non pulmonary eye signs

A

uveitis, conjunctivitis, keratoconjunctivitis sicca, glaucoma

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8
Q

what are the non pulmonary ENT signs

A

enlargement parotid and lacrimal glands, Bells palsy

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9
Q

what are the non pulmonary neuro signs

A

bells palsy, neuropathy, meningitis, brainstem and spinal syndromes, SOL

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10
Q

what are the non pulmonary derm signs

A

erythema nodosum, lupus pernio

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11
Q

what are the non pulmonary cardio and homeostatic signs

A

cardiomyopathy, arrhythmias, hypercalcaemia, hypercalcuria, renal stones, pituitary dysfunction

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12
Q

tests

A

bloods, 24 urine incr Ca, tuberculin skin test, CXR, ECG, lung function tests, tissue biopsy, bronchoalveolar lavage, US, bone x rays, CT/MRI, opthal assessment

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13
Q

what do the bloods show

A

incr ESR, lymphopenia, incr LFT, incr ACE, incr Ca, incr Ig

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14
Q

what does tissue biopsy show

A

of lung, liver, lymph nodes, skin nodules or lacrimal glands is diagnostic and shows NON CASEATING GRANULOMATA

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15
Q

what does BAL show

A

incr lymphocytes in active disease, incr neutrophils in pulmonary fibrosis

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16
Q

management if just BHL

A

don’t need treatment as most recover spontaneously

17
Q

management acute sarcoidosis

A

bed rest, NSAIDs

18
Q

management- indications for corticosteroids

A

parenchymal lung disease, uveitis, hypercalcaemia, neuro or cardiac. pred for 4-6w then decr dose over a year

19
Q

other therapy in management

A

if severe- IV methylpred or immunosuppressants, anti TNF, lung transplant

20
Q

prognosis

A

60% patients with thoracic resolve over 2y. 20% respond to steroid treatment

21
Q

differentials of bilat hilar lymphadenopathy

A

sarcoidosis, infection eg TB, mycoplasma, malignancy eg lymphoma, organic dust disease, extrinsic allergic alveolitis, histiocytosis X

22
Q

staging of sarcoidosis from the CXR

A

0-normal. 1- BHL. 2- BHL + peripheral pulmonary infiltrates. 3- peripheral pulmonary infiltrates alone. 4- progressive pulmonary fibrosis, bulla formation (honeycombing), pleural involvement