Pulmonary pathology II Flashcards
Diffuse alveolar hemorrhage histology
Blood and iron-containing macrophages within airspaces, Alveolar septa may be mildly thickened by inflammation and fibroblastic tissue. May be associated with capillaritis (neutrophils attacking the capillaries of the alveolar septa
Pulmonary Alveolar Proteinosis histology
Airspaces filled with pink fluid and macrophages
Usual Interstitial Pneumonia (UIP) histology
Patchy heterogeneous fibrosis of the septa by mature collagen. Fibroblastic foci (compact collections of fibroblasts and myxoid stroma buldging into the airspaces). Honeycomb cystic change (end-stage lung remodeling with mucus filled cysts lined by airway-type epithelium and surrounded by fibrosis)
Patchy heterogeneous fibrosis of the septa by mature collagen. Fibroblastic foci (compact collections of fibroblasts and myxoid stroma buldging into the airspaces). Honeycomb cystic change (end-stage lung remodeling with mucus filled cysts lined by airway-type epithelium and surrounded by fibrosis)
Which part of the lung displays worse honeycombing in UIP?
lower lobes
NonSpecific Interstitial Pneumonia (NSIP) histology
Uniform homogenous inflammation, fibrosis or a mixture of both. Few if any fibroblastic foci. Little if any honeycombing
Hypersensitivity Pneumonia (HP) histology
Airway-centered chronic inflammation (lymphocytes and histiocytes). Nonnecrotizing granulomas. Focal organizing pneumonia. Variable fibrosis by mature collagen
What causes hypersensitivity pneumonia?
A response to foreign antigens (birds, mold, hot-tub mycobacterial antigens, etc.)
Thromboembolic disease histology
Organizing fibrin clots within pulmonary arteries. May form in situ (thrombus) or move to the lung from elsewhere (embolism)
Talc embolisms histology
Polarizable crystals around vessels. May include foreign-body giant cells. Usually from intravenous drug use
Pulmonary hypertension histology
Muscular hypertrophy of pulmonary arteries. Muscularization of arterioles (normally should not contain smooth muscle). Some forms have plexiform lesions (the artery lumen replaced by endothelial proliferation with numerous tangled slit-like lumens)
Vasculitis histology
Inflammation of the vessel wall, Often results in alveolar hemorrhage, May be autoimmune or infectious
Inflammation of the vessel wall, Often results in alveolar hemorrhage, May be autoimmune or infectious
Sarcoid / Chronic beryllium disease nodules
Well-formed coalescing nonnecrotizing granulomas (must exclude infectious etiology). Variable concentric collagen deposition around granulomas. “lymphatic distribution” = found next to blood vessels, airways and in the pleura
Pulmonary Langerhans’ Cell Histiocytosis (PLCH) / Eosinophilic Granuloma (EG) histology
Cellular phase: Langhans histiocytes (S100, CD1a positive) and Variable inflammation including eosinophils.
Fibrotic/burnt-out phase: Stellate scar around airway.
Usually smoking-related if limited to lung
Cellular phase: Langhans histiocytes (S100, CD1a positive) and Variable inflammation including eosinophils.
Fibrotic/burnt-out phase: Stellate scar around airway.
Usually smoking-related if limited to lung
Carcinoid nodule histology
Nests and ribbons of neuroendocrine cells with powdery salt-and-pepper chromatin. Stain positive for neuroendocrine markers (chromogranin, synaptophysin, CD56). Usually indolent, but may act in a malignant fashion particularly if there is nuclear atypia, high mitotic rate or regions of necrosis
Small cell carcinoma histology
Small blue easily-crushed cells with scant cytoplasm. Stain positive for neuroendocrine markers (chromogranin, synaptophysin, CD56). High mitotic rate and abundant necrosis