Ncl Lung Flashcards

1
Q

Reticulation in posterior subpleural bases

A

Early UIP

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2
Q

Traction bronchiectasis and subpleural honeycombing, in lung bases

A

Late UIP

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3
Q

Difference between UIP and probable UIP?

A

Probable UIP doesn’t have honeycombing

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4
Q

Basal predominant peribronchial reticulation and ground glass opacities

A

NSIP, most with subpleural sparring. Fibrotic type might involve subpleural

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5
Q

Consolidation or GG opacities in a peripheral and peribronchovascular distribution, possibly reverse halo

A

Organizing pneumonia

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6
Q

Innumerable subcentimeter centrilobular GG nodules, particularly in lung apices

A

RB-ILD

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7
Q

Diffuse basal-predominant GG opacities, with possible cysts

A

DIP

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8
Q

Extensive geographic GG opacities

A

Early (exudative) Acute interstitial pneumonia, pulmonary edema, hemorrhage, infections, ARDS

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9
Q

GG opacities with alveolar wall thickening

A

Chronic (organizing) AIP

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10
Q

Diffuse GG opacities with mosaic attenuation, diffuse small GG centrilobular nodules, upper lobe predominant

A

Acute/subacute HP

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11
Q

Upper lobe predominant peribronchovascular fibrosis with GG centrilobular nodules and opacities, and mosaic attenuation

A

Chronic HP

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12
Q

Multiple upper-lobe predominant perilymphatic nodules, possible egg shell lymph node calcifications

A

Silicosis or coal workers pneumoconiosis

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13
Q

Multiple upper lobe dominant perilymphatic nodules with large conglomerate masses 

A

Complicated silicosis or complicated coal workers pneumoconiosis

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14
Q

RA with silicosis

A

Caplan syndrome

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15
Q

UIP with pleural plaques

A

Asbestosis

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16
Q

Patchy upper lobe predominant consolidations that may cross fissures

A

Chronic eosinophilic pneumonia

17
Q

Basal predominant ground glass, mild septal thickening, possible nodular foci with cavitation

A

Pulmonary vasculitis

18
Q

Upper lobe predominant perilymphatic nodules, bilateral. Hilar adenopathy.

A

Sarcoidosis

19
Q

Diffuse Multiple irregular upper lobe predominant cysts with multiple small nodules

A

Pulmonary langerhans histiocytosis

20
Q

Multiple round regular lung cysts

A

Lymphangioleiomyomatosis (LAM), particularly in women

21
Q

Lower lobe Patchy GG opacities, scattered perivascular cysts

A

Lymphoid interstitial pneumonia (LIP), associated with Sjogrens

22
Q

Circumferential tracheal thickening, ddx?

A

TB, amyloidosis (has calcs), GPA, sarcoidosis

23
Q

Tracheal thickening, sparring posterior, ddx?

A

Relapsing polychrondritis, tracheobronchopathia osteochobdroplastics (nodular calcs)