Sarcoidosis Flashcards

1
Q

what is sarcoidosis

A

A chronic, multisystem granulomatous disease of unknown cause that primarily affects the lungs but can involve multiple organs.

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2
Q

what are the respiratory symptoms

A

Dyspnea, cough, chest pain

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3
Q

what are the systemic symptoms

A

Fatigue, fever, weight loss.

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4
Q

what are the skin symptoms

A

Lupus pernio (raised, purplish skin lesions), erythema nodosum.

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5
Q

what are the eye symptoms

A

Uveitis, blurred vision, photophobia.

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6
Q

what are the liver and kidney symptoms?

A

Hepatomegaly, renal dysfunction.

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6
Q

what are the heart symptoms?

A

Arrhythmias, heart block, cardiomyopathy.

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6
Q

what are the lymph node symptoms

A

Enlarged hilar lymph nodes.

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6
Q

what does X ray and CT show

A

Bilateral hilar lymphadenopathy, pulmonary infiltrates, and fibrosis.

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7
Q

what does PFT show

A

Assesses disease progression (restrictive pattern).

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8
Q

what does serum Angiotensin-Converting Enzyme (ACE) Level show

A

Often elevated in active disease.

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9
Q

what does bronchoscopy with biopsy show

A

Confirms non-caseating granulomas.

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10
Q

what is the prognosis

A

Some cases resolve spontaneously.
Others follow a chronic progressive course, leading to fibrosis and organ dysfunction.

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11
Q

what is the treatment

A

Mild cases → Observation, supportive care.
Severe or progressive disease → Immunosuppressive therapy.

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12
Q

what is the first-line treatment

A

Corticosteroids (e.g., prednisone) → To reduce inflammation.

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13
Q

what are the steroid sparing agents

A

Methotrexate, azathioprine, or mycophenolate

14
Q

when are TNF inhibitors (e.g., infliximab) given

A

For severe cases, especially cardiac or neurological sarcoidosis.

15
Q

when does pt need follow up

A

Every 3 to 6 months with:
Pulmonary function tests (to track lung function).
Chest X-rays & CT scans (to monitor disease progression).
Eye & cardiac evaluations (if those organs are affected).

16
Q

what should Pt do?

A

Unpredictable course—some patients experience spontaneous remission, while others develop chronic progression.
Routine follow-ups are crucial to monitor for fibrosis and organ damage.
Avoid environmental triggers (e.g., smoking, dust, air pollution) to reduce flare-ups.
Stay up to date on vaccines (flu, pneumococcal) to prevent respiratory infections.