Pulm Flashcards
Acute Interstitial Pneumonia: Pathogenesis and presentation
.Similar presentation to ARDS. Influenza like illness followed by shortenss of breath.
Diagnosis of Bronchiectasis
Histology/pathology shows Large airways are visible all the way to the lung periphery. CXR shows “Signet ring sign”, “Tram tracking” , PFT shows decreased FEV1/FVC
Management and prognosis of Neonatal Respiratory Distress Syndrome (NRDS)
Treatment options: CPAP, Exogenous surfactant
Management and prognosis of Squamous cell carcinoma
5 year survival is 5-7.5%
Pathology of Asthma
Histology/pathology shows Bronchial smooth muscle proliferation, eosinophils in the submucosa, thickened basement membrane. Can see Curschmann spirals, Charcot-Leyden crystals. PFT shows FEV1/FVC
Management and prognosis of Pleural effusion - exudative
Uncomplicated exudative: treat the cause. Complicated exudative: serial taps to drain fluid
Diagnosis of Adenocarcinoma
Histology/pathology shows Peripheral tumors. Well demarcated spiculated mass with central scarring. Gland forming or mucin containing cells. . Mutated genes: EGFR, ALK fusions, KRAS
Diagnosis of Acute Interstitial Pneumonia
Histology/pathology shows DAD with brisk interstitial fibroblastic proliferation.
Management and prognosis of Central sleep apnea
CPAP
Management and prognosis of Pleural effusion - transudative
Treat the cause
Diagnosis of Pleural effusion - exudative
Lights criteria for exudates: looks at protein, LDH and cholesterol levels. CXR shows blunting of the costophrenic angle, meniscus sign with white out of one lung, mediastinum shifted away
Pneumonia: Pathogenesis and presentation
Increased risk in elderly, smokers, pulmonary disease, recent viral illness, diabetes, chronic renal disease, immunodeficiency.Cough, sputum, fever, shortness of breath.
Diagnosis of Pneumothorax
Hyperresonant lungs, unilateral hyperinflation. CXR shows trachea and mediastinal shift toward affected lung
Diagnosis of Chronic Bronchitis
Histology/pathology shows Mucus glands hypertrophy, inflammation, fibrosis. Reid index (gland to wall ratio) elevated.. Clinical dx: Persistent productive cough for at least three consecutive months in at least two consecutive years. PFT shows FEV1/FVC
Diagnosis of Neonatal Respiratory Distress Syndrome (NRDS)
Histology/pathology shows Diffuse alveolar damage: pneumocyte and endothelial cell necrosis, edema, hyaline membrane formation.
Diagnosis of Idiopathic Pulmonary Fibrosis
Histology: Usual interstitial pneumonia, Morphology: cobblestoned pleural surface with non-uniform fibrosis. Honecomb fibrosis is seen. CXR or CT shows honeycombing of subpleural regions. Trichrome stain can be used to confirm collagen deposition. PFT shows decreased TLC
Diagnosis of Pneumoconioses
Histology/pathology shows inhaled particles anthracosis = coal deposits, whorls= silica. CXR showing fibrotic lung. PFT shows decreased TLC
Management and prognosis of Adenocarcinoma
Metastasizes early. 5 year survival is 10-12%
Diagnosis of Mesothelioma
Histology/pathology shows Tumor spreads widely in pleural space, invades by contiguous spread or diffuse seeding. . Chromosome deletions (1p, 3p, 6q, 9p, 22q) and somatic mutations of TSGs (p16/CDKN2A, NF2)
Management and prognosis of Tuberculosis
Long term therapy. “RIPE”
Tuberculosis: Pathogenesis and presentation
Droplets inhaled, macrophages take up and granuloma forms. Primary infection usually causes latent TB. Secondary disease (10% of infection) is reactivated infection in upper lung and/or extrapulmonary sites.Usually in foreign born individuals, AIDS patients. Infection progresses to disase 10% of the time. Restrictive lung disease
Diagnosis of Obesity-hypoventilation syndrome
Polysomnography, Apnea hypopnea index > 5 (episodes per hour)
Diagnosis of Central sleep apnea
Polysomnography, Apnea hypopnea index > 5 (episodes per hour)
Diagnosis of Large cell carcinoma
Histology/pathology shows Undifferentiated cells. No squamous or glandular differentiation is seen..
Diagnosis of Kartagener Syndrome
Histology/pathology shows Cilia and flagella lose their dynein arms, are thus unable to move.
Bronchiectasis: Pathogenesis and presentation
Obstruction, infection, or congenital defects can cause permanent dilatation of the bronchi and bronchioles caused by destruction of muscle and elastic tissue.Cough, purulent sputum, persistent or severe infections
Management and prognosis of Pulmonary embolism
Depends on degree of occlusion. Treated with anticoagulation. Could be fatal, could lead to recurrent PE.
Diagnosis of Carcinoid tumor
Split into typical (low mitotic rate, no necrosis) and atypical (more frequent mitosis, focal necrosis).
Diagnosis of Pulmonary Edema/ High pressure pulmonary edema
Pathology shows distended lungs, frothy fluid oozes out. Histology shows congested capillaries and acellular fluid filled air spaces. CXR shows cardiomegaly, pleural effusions, alveolar opacities
Management and prognosis of Asthma
Treated with “relievers” (beta agonists), used as needed, and “controllers”(corticosteroids), used regularly.
Diagnosis of Small cell carcinoma
Histology/pathology shows centrally arising tumors. Densely packed tumor with small blue cells with round/ovoid nuclei, scant cytoplasm, “salt and pepper” chromatin. Inactivation of p53 and RB in all cases. Also show loss of 3p, 4q, 5q, 13q and 15q
Management and prognosis of Sepsis
Goal directed fluid resuscitation, control source of infection with ABX, vasopressors, support failing organs. High mortality
Obstructive sleep apnea: Pathogenesis and presentation
Increased risk in obese, large neck circumference, hypertension, elderly men, smokers.Upper airway obstruction causes periods of apnea, chest/abdominal effort remains
Diagnosis of Emphysema
Histology/pathology shows Hyperinflated lungs with formation of bullae. Histology shows hugely distended alveoli with no fibrosis or thickened septa. 4 classes based on location: centriacinar, panacinar, distal acinar, irregular. PFT shows decreased FEV1/FVC