Criado por Aaron Samide
mais de 8 anos atrás
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Questão | Responda |
Sarcoidosis is a systemic disease characterized by __________________. | non-caseating granulomas |
Prognosis of sarcoidosis | 2/3 experience resolution/improvement over several years 20% develop chronic disease 10-20% are asymptomatic but have CXR findings |
Skin findings associated with sarcoidosis | Erythema nodosum Plaques, subcutaneous nodules, maculopapular eruptions |
Eye findings associated with sarcoidosis (3) | - Anterior uveitis - Posterior uveitis - Conjunctivitis |
Heart findings associated with sarcoidosis (3) | - Arrhythmias - Conductions disturbances (e.g., blocks) - Sudden death |
MSK findings associated with sarcoidosis | Arthralgias & arthritis Bone lesions |
Nervous system findings associated with sarcoidosis | - CN VII involvement (Bell's palsy) - Optic nerve dysfunction - Papilledema - Peripheral neuropathy |
While an uncommon finding in sarcoidosis, what is the most common cause of death in sarcoidosis patients? | Cardiac disease |
Hallmark CXR finding of sarcoidosis | Bilateral hilar LAD |
Enzyme elevated in serum in 50-80% of sarcoidosis patients | ACE (angiotensin-converting enzyme) |
Definitive diagnosis of sarcoidosis requires... | Transbronchial biopsy (showing noncaseating granulomas) |
Staging of sarcoidosis based on CXR | I: Bilateral hilar LAD w/out parenchymal infiltrates II: w/ parenchymal infiltrates III: Diffuse parenchymal infiltrates without hilar lymphadenopathy IV: Pulmonary fibrosis w/ honeycombing and fibrocystic changes |
Stage of sarcoidosis with least favorable prognosis | Stage III: Diffuse parenchymal infiltrates without hilar adenopathy |
Treatment of sarcoidosis | Systemic corticosteroids If refractory, MTX |
What is histiocytosis X? | Chronic interstitial pneumonia caused by abnormal proliferation of histiocytes |
___% of histiocytosis X patients are cigarette smokers. | 90% |
Common findings in histiocytosis X (5) | - Dyspnea - Nonproductive cough - Spontaneous PTX - Lytic bone lesions - Diabetes insipidus |
CXR and CT appearance of histiocytosis X | CXR: honeycomb CT: cystic lesions |
Prognosis & treatment of histiocytosis X | Prognosis & course highly variable Steroids may be effective; lung transplant may be necessary |
Wegener granulomatosis is characterized by what pathologic finding? | Necrotizing granulomatous vasculitis |
Wegener's most often affects vessels of what organs? | Lungs Upper airway Kidneys |
Gold standard for diagnosis of Wegener's | Tissue biopsy |
Classic lab finding indicative of Wegener's | c-ANCA (+) |
Treatment of Wegener's | Immunosuppressives and glucocorticoids |
Churg-Strauss is a granulomatous vasculitis seen in patients with _________. | asthma |
Typical presentation of Churg-Strauss (3) | Pulmonary infiltrates Rash Significant blood eosinophilia |
Churg-Strauss is associated with labs positive for _______, which is also found in what other condition? | p-ANCA Goodpasture |
Treatment of Churg-Strauss | Glucocorticoids |
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