Restrictive2 Flashcards

1
Q

Has noncaseating granulomas with schaumann bodies and asteroid bodies

A

Sarcoidosis

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2
Q

Laminated concretions of Ca and proteins

A

Sarcoidosis

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3
Q

Stellate inclusions in giant cells

A

Sarcoidosis

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4
Q

Hilar and mediastinal LNs calcified. Spleen enlarged. Granulomas in portal tract of liver. Bone marrow of phalangeal bones in hands and feet involved

A

Sarcoidosis

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5
Q

Bronchoscope can biopsies high yield

A

Sarcoidosis

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6
Q

Iritis and lacrimal gland inflammation (dacroadenitis)

A

Sarcoidosis

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7
Q

Dacroadenitis and BL involvement of parotid, submaxillary, and sublingual glands

A

Mikulicz syndrome. Sarcoidosis

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8
Q

Anorexia, weight loss, night sweats

A

Sarcoidosis

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9
Q

Unpredictable course. 2/3rds recover w/o any problems. 20% get permanent loss of visual/lung fn. 10-15% die of cardiac, lung, or CNS disease (usually progressive pulmonary fibrosis)

A

Sarcoidosis

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10
Q

Hilar lympadenopathy sarcoidosis

A

Best prognosis

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11
Q

Immunologically mediated. Prolonged exposure to inhaled organic dusts and occupational antigens

A

Hypersensitivity pneumonitis

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12
Q

Has type 3 immune complex rx and type 4 hypersensitivity granulomatous rx

A

Hypersensitivity pneumonitis

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13
Q

Inhaled spores of actinomycetes

A

Farmers lung - hypersensitivity pneumonitis

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14
Q

Noncaseating granulomas

A

Hypersensitivity pneumonitis

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15
Q

Occurs in previously sensitized pts. Fever, SOB, cough, increased WBC 4-6 hrs after re-exposure

A

Acute attacks of hypersensitivity pneumonitis

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16
Q

Progressive SOB and cyanosis. Decreased compliance and TLC.

A

Chronic hypersensitivity pneumonitis

17
Q

Hypersensitivity to inhaled antigens (not food or drugs). Rapid fever, SOB, and hypoxemia > respiratory failure. Bronchoalveolar lavage shows >25% eosinophils. Treat with steroids

A

Acute eosinophilic pneumonia

18
Q

Hypersensitivity to food or drugs (sulfa). Transient lung lesions and blood eosinophilia. Alveolar septa with eosinophils and giant cells. Benign, self limited

A

Simple pulmonary eosinophilia (loefflers)

19
Q

Parasitic, bacterial, and fungal infections. Associated with asthma and aspergillosis. Can cause chronic lung injury and fibrosis

A

Secondary pulmonary eosinophilia

20
Q

Associated with autoimmune disease. Eosinophil and lymphocyte aggregates in septal walls and alveolar spaces. Increased fever, night sweats, and SOB. Treat with steroids

A

Chronic eosinophilic pneumonia

21
Q

All patients smokers. Alveoli filled with pigment laden smokers macrophages

A

Desquamative interstitial pneumonitis

22
Q

4-5th decade. Males. Insidious onset. Clubbing. Excellent response to steroid treatment (100%)

A

Desquamative interstitial pneumonitis

23
Q

Significant symptoms SOB and cough. Smokers macrophages in peribronchiolar regions, respiratory bronchioles, and alveolar ducts

A

Respiratory bronchiolitis associated interstitial lung disease

24
Q

Mild fibrosis of peribronchiolar region w/ centrilobar emphysema. Improves with smoking cessation

A

Respiratory bronchiolitis associated interstitial lung disease

25
Q

Increases in CD4 Thelper cells, IL2/IL8, TNF, IFN -gamma, macrophage inflammatory protein

A

Sarcoidosis