Interstitial Diseases Associated with Granulomas

Descrição

USMLE Step 2 Pulmonology (2d Interstitial Lung Disease) FlashCards sobre Interstitial Diseases Associated with Granulomas, criado por Aaron Samide em 16-05-2016.
Aaron Samide
FlashCards por Aaron Samide, atualizado more than 1 year ago
Aaron Samide
Criado por Aaron Samide mais de 8 anos atrás
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Resumo de Recurso

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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