Lecture 5: Interstitial Lung Disease Flashcards

1
Q

Which histopathologic pattern of interstital lung involvement is characterized by heterogenous involvement of the lung with different stages of progression of fibrosis in adjacent areas of the lung?

A

Usual Interstitial Pneumonitis (UIP)

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2
Q

A pt presenting with progressive dyspnea (over months), reduced exercise tolerance, and a persistent dry cough should raise suspicion for what?

A

Interstitial lung disease

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3
Q

Which imaging modality is a crucial tool for the diagnostic evaluation of interstitial lung diseases?

A

High-resolution CT

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4
Q

Interstital lung disease evaluation must include hx of what 5 things?

A
  • Occupation
  • Hobbies
  • Enviornmental
  • Travel
  • Drugs both Rx and non-Rx
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5
Q

Which lung sound auscultated in a patient with interstitial lung disease is almost pathognomonic?

A

Crackles often described as “velcro” developing in the bases throughout inspiration

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6
Q

What are the prototypic sign/sx’s of interstitial lung disease?

A
  • Dyspnea + cough + crackles
  • Digital clubbing (presence does not confirm and absence does not eliminate ILD)
  • Exercise induced hypoxemia
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7
Q

What is the FRC, TLC, FEV1/FVC and DLCO like with interstitial lung diseases?

A
  • ↓ FRC and ↓ TLC
  • Normal FEV1/FVC
  • Low DLCO
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8
Q

Very low pleural glucose is characteristics of pleural disease associated with what?

A

Rheumatoid Arthritis

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9
Q

Shrinking lung syndrome is associated with what systemic disease?

A

SLE

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10
Q

Which 3 autoantibodies may be seen in Scleroderma; which is most common in those with ILD; which is associated with worst prognosis?

A
  • Anticentromere
  • SCL-70 = more common in ILD
  • Antinucleolar = predicts worst prognosis
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11
Q

Which autoantibody is seen in >90% of drug induced SLE cases?

A

anti-Histone

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12
Q

Which autoantibody is seen in 90-95% of SLE cases?

A

Anti-nuclear antibodies

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13
Q

Which autoantibody is seen in pt’s with SLE induced nephritis?

A

Anti-dsDNA

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14
Q

Which antiarrhythmic and antibiotic used for UTI’s are commonly associated with drug induced interstitial lung disease?

A
  • Amiodarone
  • Nitrofurantoin
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15
Q

When is the early phase vs. late phase of radiation induced lung disease?

A
  • Early phase = 1-3 months after radiation
  • Late phase = 6-12 months
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16
Q

What is the rate of decline and cough like in ILD vs. COPD?

A
  • COPD = slower decline w/ more frequent exacerbations + productive cough
  • ILD = more rapid decline + non-productive cough
17
Q

What is the mainstay drug used to tx non-IPF induced ILD?

A

Corticosteroids

18
Q

What are the 2 anti-fibrotic agents which are ONLY used for idiopathic pulmonary fibrosis; describe each drug?

A

1) Pifenidone = antifibrotic and anti-inflammatory
2) Nintedanib = tyrosine kinase inhibitor targets inflammatory and profibrotic factors

19
Q

What is the characteristic finding on a CXR of someone with acute interstitial pneumonia (aka Hamman-Rich syndrome)?

A

Diffuse, symmetrical, and bilateral

20
Q

What is the onset like with acute interstitial pneumonia (aka Hamman-Rich syndrome) vs. IPF?

A
  • AIP –> abrupt onset w/ flu-like sx’s
  • IPF –> gradual onset, afebrile
21
Q

Acute interstitial pneumonia (aka Hamman-Rich syndrome) vs. IPF occurs in which age groups?

A
  • AIP –> occurs in patients from all age groups, mostly adults
  • IPF –> occurs almost exclusively in adults
22
Q

How is the diagnosis of acute interstitial pneumonia (aka Hamman-Rich syndrome) vs. IPF established?

A
  • AIP –> BIOPSY establishes diagnosis
  • IPF –> hx/clinical findings, imaging, and PFTs; biopsy optional