Sarcoidosis Flashcards

1
Q

What is sarcoidosis?

A

Granulomatous inflammatory condition affecting multiple systems

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2
Q

What are granulomas?

A

nodule of inflammation filled with macrophages

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3
Q

Who does sarcoidosis commonly affect?

which age ranges?

A

black people
women
two peaks in incidence: early adulthood, 60’s

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4
Q

What are the pulmonary features of sarcoidosis?

signs
symptoms

what is the prognosis?

A
  1. abnormal CXR with bilateral hilar lymphadenopathy
  2. pulmonary fibrosis
  3. pulmonary nodules

symptoms

  1. dry cough
  2. progressive dyspnoea
  3. reduced exercise tolerance
  4. chest pain

in 10-20% symptoms progress with concurrent deterioration of lung function

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5
Q

What are the extra pulmonary features of sarcoidosis?

A

systemic

  1. fever
  2. fatigue
  3. weight loss

Liver:

  1. liver nodules
  2. cirrhosis
  3. cholestasis

Skin

  1. erythema nodosum
  2. Lupus pernio (raised purple skin lesions commonly nose and cheeks)
  3. granulomas develop in scar tissue

Eyes

  1. uveitis
  2. conjunctivitis
  3. optic neuritis

Kidney

  1. hypercalcaemia
  2. nephrocalcinosis
  3. interstitial nephritis

Heart

  1. BBB, heart block
  2. myocardial involvement

CNS

  1. nodules
  2. pitituitry involvement (diabetes insipidus)
  3. encephalopathy

PNS

  1. facial nerve palsy
  2. mononeuritis complex

MSK

  1. arthralgia
  2. arthritis
  3. myopathy
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6
Q

Why does sarcoidosis cause hypercalcaemia?

A

Macrophages inside the granulomas cause an increased conversion of vitamin d to its active form - 1,25-dihydroxycholecalciferol

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7
Q

How does acute sarcoidosis typically present and what is the name for it?

What is the prognosis?

A

Lofgren’s syndrome

  1. erythema nodosum
  2. bilateral hilar lymphadenopathy
  3. swinging fever
  4. polyarthralgia

very good prognosis - usually resolves spontaneously

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8
Q

How does the typical exam patient present?

A
  • 20-40 year old black female
  • presenting with dry cough and SOB
  • may have nodules on shin suggesting erythema nodosum
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9
Q

What is Heerfordt’s syndrome?

A

uveoparotid fever

  1. parotid enrlagement
  2. uveitis
  3. fever

secondary to sarcoidosis

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10
Q

How does insidiuous sarcoidosis present?

A
  1. SOB
  2. dry cough
  3. malaise
  4. weight loss
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11
Q

What investigations would you do for sarcoidosis?

Bloods
Calcium

others:

A
  1. raised serum ACE in 60%, non specific
  2. raised ESR, CRP
  3. hypercalcaemia
  4. raised immunoglobulins
  5. raised LFTs (if liver involvement)

calcium:
24 hr urine

  1. CXR
  2. Lung function tests
  3. Biopsy
  4. CT/MRI
  5. Bronchoalveolar lavage
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12
Q

What would you expect to see in CXR

A

stage 0 = normal
stage 1 = bilateral hilar lymphadenopathy (BHL)
stage 2 = BHL + interstitial infiltrates
stage 3 = diffuse interstitial infiltrates only
stage 4 = diffuse fibrosis

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13
Q

What would you expect to see in biopsy?

where can you take it?

A

DIAGNOSTIC
non caseating granulomas

lung, liver, lymph nodes, skin nodules, lacrimal glands

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14
Q

What can you expect to see in lung tests?

A

spirometry - restrictive features

reduced lung volume

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15
Q

How would you manage sarcoidosis first line?

A

no treatment, patients with mild or no symptoms often resolve spontaneously

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16
Q

What are the indication for steroids (prednisolone) in sarcoidosis?

A
  • Patients with CXR stage 2-3 with symptoms
  • Uveitis.
  • Hypercalcaemia.
  • Neurological or cardiac involvement.
17
Q

What must you give alongside steroids?

A

bisphosphonates to protect bone

18
Q

What other management is there for sarcoidosis if steroids do not work?

A

methotrexate
azathioprine

severe:
lung transplant

19
Q

What are the differentials for sarcoidosis?

A
  1. TB
  2. Lymphoma
  3. hypersensitivity pneumonitis
  4. HIV
  5. Toxoplasmosis, histoplasmosis
20
Q

How do you manage acute sacroidosis?

A

bed rest

NSAIDs