Sarcoidosis Flashcards

1
Q

What is sarcoidosis

A
  1. Systemic, granulomatous disease of unknown etiology
    *can involve many systems
    *non-caseating granulomas (lung involvement (90%))
    *bilatera hilar lymphadenopathy (75-90%)
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2
Q

What are the demographics of sarcoidosis

A
  1. Higher incidence in North American African Americans and Northern European caucasians
    *no genetic predisposition known
  2. Onset 30 to 40 years old
  3. Autoimmune, rheumatologist disease state
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3
Q

What is the pathology behind sarcoidosis (1)

A
  1. Exaggerated T lymphocyte response to exogenous or autologous antigens
  2. Cells accumulate in the affected organs, secrete lymphokines and recruit macrophages
  3. T cell accumulation results in formation of non-caseating granulomas
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4
Q

What is the pathology behind sarcoidosis (2)

A
  1. Multiple granulomas are scattered through the intersitiutm of the lung
  2. Granulomas take up space that disrupts the normal/healthy structure/function of the tissues that they from in
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5
Q

What accounts for the high diagnostic yield on bronchoscopes biopsy

A
  1. Frequent bronchial or bronchioar submucosal infiltration by sarcoid granulomas
    *cellular granulomatous phase of sarcoidosis can further progress to fibrotic phase
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6
Q

What are the signs and symptoms of sarcoidosis

A

Asymptomatic (50%) incidental findings on CXR
1. Pulmonary
*dyspnea
*cough
2. Insidious onset
3. Skin manifestations
*erythema nodosum
*lupus pernio

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7
Q

What are other manifestations of sarcoidosis

A
  1. Fever
  2. Malaise
  3. Uveitis
  4. Iritis
  5. Conjunctivitis
  6. Glaucoma
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8
Q

What are the MS signs of sarcoidosis

A
  1. Myopathies
  2. Myositis
  3. Polyarhritis (ankles, knees, wrists)
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9
Q

What are the neurological signs of sarcoidosis

A
  1. CN palsies
  2. Meningitis
  3. Neuroendocrine dysfunction
  4. Neuropathy
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10
Q

What are the cardiac signs of sarcoidosis

A
  1. Chest pain
  2. Arrhythmia
  3. Conduction delays
  4. Pulmonary HTN
  5. CHF
  6. Pericarditis
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11
Q

What are the liver signs of sarcoidosis

A
  1. Abdominal pain
  2. Jaundice
  3. Varices
  4. Granulomatous hepatitis
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12
Q

What are the endocrine signs of sarcoidosis

A
  1. Hypercalcemia
  2. Goiter
  3. Thyroid nodules
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13
Q

What will be on the PE

A
  1. Atypical of ILD
    *no crackles
  2. Parotid gland enlargement
  3. Hepatosplenomegaly
  4. Lymphadenopathy
  5. Signs from the previous slides
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14
Q

What is the DDx

A
  1. Amyloidosis
  2. Lymphoma
  3. Fungal infection
  4. Tuberculosis
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15
Q

What diagnostic tests to complete

A
  1. ACE levels
    *elevated (40 to 80% of patients)
  2. PFT (restrictive)
  3. Ophthalmic examination
  4. Chest radiography
  5. CBC, ESR, CMP, UA, EKG
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16
Q

What can the diagnosis be confirmed with

A
  1. Histological demonstration of granulomas
    *biopsy will show
    *demonstration of non-caseating granulomas
    *BAL does not establish diagnosis
17
Q

What are the pulmonologic treatment of sarcoidosis

A
  1. Steroids
  2. Lung transplant
18
Q

What are the arthralgias treatment of sarcoidosis

A
  1. Steroids
  2. NSAIDs
  3. Colchicine
  4. Biologics
  5. Steroid sparing agents
19
Q

What are the immunosuppressive treatment of sarcoidosis

A
  1. Methotrexate
  2. Azathioprine
  3. Infliximab
20
Q

What is the prognosis of sarcoidosis

A
  1. Best for hilar adenopathy involvement alone (stage I)
    *pulmonary involvement have irreversible complications
  2. Long term follow-up, annual check up