Sarcoidosis Flashcards

1
Q

Sarcoidosis–essentials of diagnosis

A
  • symptoms related to lung, skin, eyes, peripheral servers, liver, kidney, heart, other tissues
  • noncaseating granulomas in biopsy specimen
  • Exclusion of other granulomatous disorders
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2
Q

General considerations–sarcoidosis

A
  • systemic disease of unknown etiology
  • 90% have granulomatous inflammation of lung
  • highest in N. American blacks and N. european whites
  • most commonly black women
  • Onset= 3-4th decade
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3
Q

Sarcoidosis signs and symptoms

A
  • malaise, fever, dyspnea
  • skin–erythema nodosum, lupus penio
  • iritis
  • peripheral neuropathy
  • arthritis
  • cardiomyopathy
  • some are asymptomatic but have abnormal findings like bilateral hilar and right paratracheal lymphadenopathy on chest x-ray
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4
Q

Sarcoidosis PE

A
  • atypical of interstitial lung disease in that crackles are UNCOMMON
  • parotid gland enlargement, hepatosplenomegaly, lymphadenopathy
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5
Q

Lab findings for sarcoidosis

A
  • leukopenia
  • high ESR and hypercalcemia (5%)
  • high ACE (40-80%)–but never diagnostic!
  • airflow obstruction but restrictive changes with decreased lung volumes and diffusing capacity more common
  • Skin test anergy present in 70%
  • ECG: conduction disturbance and dysarythmias
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6
Q

Sarcoidosis imaging

A

-variable

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7
Q

Radiographic stage I of sarcoidosis

A

bilateral lymphadenopathy alone

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8
Q

Radiographic stage II of sarcoidosis

A

hilar adenopathy AND parenchymal involvment

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9
Q

Radiographic stage III of sarcoidosis

A

Parenchymal involvement alone

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10
Q

Parenchymal involvement of sarcoidosis on radiograph looks like?

A
  • Diffuse reticular infiltrates but focal infiltrates, acinar shadows, nodules and rarely cavitation seen
  • pleural effusion seen in less than 10%
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11
Q

Radiographic stage IV of sarcoidosis

A

Advanced fibrotic changes principally in upper lobes

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12
Q

Sarcoidosis special exams

A
  • requires histologic demonstration of noncaseating granulomas in biopsies with other typical associated findings
  • Other granulomatous diseases (berylliosis, Tb, fungal infxns must be excluded)
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13
Q

Easily accessible sites for biopsy to dx sarcoidosis

A
  • palpable lymph nodes, skin lesions, salivary glands
  • likely to be positive

*Transbronchial biopsy has high yield as well, esp in those with parenchymal involvement on X ray

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14
Q

When to use biopsy and when not to for sarcoidosis

A
  • May not need it for stage I if imaging and situation favors Dx (young black woman with erythema nodosum)
  • Biopsy essential when imaging and clinical suggest possibility of something else like lymphoma
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15
Q

Bronchioalveolar lavage in sarcoidosis shows

A
  • Increase in lymphocytes
  • High CD4/CD8 ratio
  • Bronchoalveolar lavage does NOT establish Dx but may be useful in following activity of sarcoidosis in selected pts
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16
Q

All pts require what for sarcoidosis??

A

-complete ophthalmologic evaluation

17
Q

Treatment for sarcoidosis

A
  • oral corticosteroids (prednisone)–0.5-1.0 mg/kg/day IF disabling symptoms, hypercalcemia, iritis, uveitis, arthritis, CNS involvement, cardiac involvement, granulomatous hepatitis, cutaneous lesions other than erythema nodosum and progressive pulmonary lesions
  • Long term Tx required over months-yrs
18
Q

Use what medications for patients who cannot tolerate corticosteroids or who have corticosteroids refractory disease?

A

Immunosuppressive drugs:

  • Methotrexate
  • Azathioprine
  • Infliximab

*research supporting effectiveness is lacking

19
Q

Prognosis of sarcoidosis

A
  • BEST for HILAR adenopathy ALONE
  • lung parenchymal associated Dz=worse prognosis
  • Erythema nodosum=good outcome
  • 20% suffer irreversible lung impairment with progressive fibrosis, bronchiectasis, and cavitation
  • Pneumothorax, hemoptysis and mycetoma in lung cavities and resp failure complicate advanced disease
  • Myocardial sarcoidosis (5%)–restrictive cardiomyopathy, cardiac dysarrhythmias, conduction disturbances
  • Death from resp insufficiency in 5%
20
Q

Monitoring patients with sarcoidosis

A
  • Long term follow up–at minimum need:
  • yearly physicals
  • PFTs
  • Chemistry panel
  • Opthalmologic evaluation
  • Chest imaging
  • ECG