Fundamentals of HRCT - Reticular opacitites Flashcards

1
Q

what are the 3 types of reticular opacities seen on HRCT

A

interlobular septal thickening, honeycombing, INTRAlobular septal thickening

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2
Q

describe the anatomy of the secondary pulmonary lobule

A

separated by the interlobular septa (which carries the veins and lymphatic systems). the lobular bronchiole and artery are centrilobular in locatoin

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3
Q

when interlobular septal thickening is the predominant finding, what is the next framework/finding that helps guide diagnosis?

A

smooth ist vs nodular ist vs irregular ist

smooth ist = pulm edema or lymphangitic spread. rarely - lympoprolif, amyloid, PVOD, lymphangiomatosis
nodular ist = sarcoid, lymphangitic spread, lymphoprolif, amyloid
irregular ist = fibrotic

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4
Q

what are the characteristics of honeycombing?

A
  • BLACK ie airfilled without any anatomy inside (vessels, bronchi, septations)
  • thick walls (thin = cyst)
  • 3-10 mm in diameter
  • must have subpleural involvement
  • layering/cluster should be visible
  • do not branch
  • associated w/ other fibrotic features - traction brx, irregular reticulation, volume lost
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5
Q

what is the differential for the diseases with honeycombing? (9)

A

IPF, CTD-ILD (RA), drug fibrosis, asbestosis,chronic HP, sarcoid, NSIP, pneumoconiosis, post-ARDS fibrosis

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6
Q

what are the HRCT findings that are consistent with UIP? (3 + and 6 negative)

A

honeycombing, other signs of fibrosis (traction bcx, irreg reticulations), subpleural and basilar predominance

ABSENCE of GGOs, consolidation, cysts, airtrapping, upper lobe predominance, micronodules

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7
Q

ddx for UIP

A

IPF, CT-ILD (RA), asbestos, drugs

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8
Q

what are some differences between honeycombing and paraseptal emphysema? (4)

A

PSE is usually one layer, can be larger, not associated with fibrosis, upper lobes > lower lobes

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9
Q

what is intralobular interstitial thickening?

A

thickening of the interstitum within pulmonary nodules - causes reticulation. relatively nonspecific

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10
Q

what is the differential for fibrotic disease in the upper lobes? (6)

A

sarcoid, prior TB , prior fungal, radiation fibrosis, pneumoconioses, AS

note idiopathic pnas involve the costophrenic angle

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11
Q

what is the differential for fibrotic disease in the lower lobes? (5)

A

IPF, CT-ILD, drugs, asbestos, aspiration

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12
Q

what is the differential for subpleural involvement? (5)

A

ipf, ct-ild, drugs, asbestosis, ards

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13
Q
A
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