Ch 15: Morphology Flashcards

1
Q

Engorged alveolar capillaries an intra-alveolar transudate with presence of hemosiderin-laden macrophages

A

Pulmonary Edema

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2
Q

Heavy lungs exhibiting inflammation, fibrin deposition, and diffuse alveolar damage with hyaline membranes

A

Acute Lung Injury/Acute Respiratory Distress Syndrome

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3
Q

Irreversible enlargement of airspaces with destruction of the bronchiole walls and fibrous deposition

A

Emphysema

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4
Q

Inflammation of airways and hypertrophy of mucus glands causing mucus plug formation and fibrosis

A

Chronic Bronchitis

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5
Q

Airway bronchoconstriction with presence of cuschmann spirals, Charcot-Leyden crystals, and airway remodeling

A

Asthma

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6
Q

B/l lower lobe destruction of SM and elastic tissue by necrotizing infections causing dilation of bronchi and fibrosis

A

Bronchiectasis

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7
Q

Inflammation and fibrosis of pulmonary interstitium

A

Restrictive/Interstitial lung disease

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8
Q

Patchy interstitial fibrosis with honeycomb fibrosis and cobblestone appearance of pleural surfaces

A

Interstitial Fibrosis (UIP)

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9
Q

Carbon-laden macrophages around a network of collagen fibers mostly affecting the upper lobes

A

Coal Workers’ Pneumoconiosis

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10
Q

Nodules in hilar LNs and upper lung zones with whorled appearance and eggshell calcification

A

Silicosis Pneumoconiosis

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11
Q

Diffuse interstitial fibrosis with presence of fusiform/beaded rods with translucent center, Ferruginous bodies, and pleural plaques

A

Asbestos-Related Pneumoconiosis

Fusiform rods = asbestos bodies

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12
Q

Non-necrotiing granulomas with varying stages of fibrosis and hyalinization and presence of Schaumann and Asteroid bodies

A

Sarcoidosis

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13
Q

Large numbers of macrophages with abundant cytoplasm with dusty brown pigment in air spaces

A

Smokers’ macrophages

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14
Q

Intra-alveolar pink granular material, type 2 pneumocyte hyperplasia, interstitial fibrosis, and alveolar simplification

A

Surfactant Dysfunction Disorder

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15
Q

Infarct with areas of ischemic necrosis of alveolar walls, bronchioles, and vessels

A

Pulmonary Embolism/Infarction

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16
Q

Focal necrosis of alveolar walls with intra-alveolar hemorrhages and alveoli containing hemosiderin-laden macrophages

A

Goodpasture syndrome

17
Q

Bilateral patchy consolidation of the lung gravitating to the lower lobes

A

Bronchopneumonia

18
Q

Diffuse consolidation of a lobe of the lung

A

Lobar pneumonia

19
Q

Vocal cord swelling with abundant mucus production with an interstitial inflammatory rxn involving alveolar walls

20
Q

Suppurative destruction of lung parenchyma within central area of caitation

A

Lung abscess

21
Q

Granulomas that undergo caseating necrosis and coalesce creating large areas of consolidation

A

Histoplasmosis

22
Q

Suppurative granulomas with possible miliary infiltrates

A

Blastomycosis

23
Q

Thick-walled, non-budding spherules filled with small endospores in macrophages

A

Coccidioidomycosis

24
Q

Collar-button lesions with organoid, trabecular, palisading, ribbon, or rosette-like arrangements of cells

A

Carcinoid tumors

25
Nodules of CT intersected by epithelial cells
Lung Hamartoma
26
Proliferation of perivascular epithelioid cells that express markers for melanocytes and SM cells
Lymphangioleiomyomatosis
27
Proliferation of spindle-shaped fibroblasts and myofibroblasts, lymphocytes, and plasma cells with peripheral fibrosis
Inflammatory Myofibroblastic tumor
28
Epithelioid type tumor with cells forming tubular/papillary structures resembling adenocarcinoma
Mesothelioma
29
Polypoid plugs of loose organizing CT (Masson bodies) in alveoli
Cryptogenic Organizing Pneumonia (BOOP)