First Aid, Chapter 7 Hypersensitivity Disorders, Interstitial Lung Disease Flashcards

1
Q

What is the injury pattern in interstitial pneumonitis characterized by? What cytokines are involved? Via what cell? What is seen on early vs. late radiography?

A

The acute injury pattern of interstitial pneumonitis is characterized by fibroblastic foci. IL-1, -6, -8, and TNF are important cytokines involved via macrophages. “Ground-glass” appearance on early radiography versus “honeycombing” in the late phases.

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2
Q

What is the most common of the interstitial pneumonias?

A

Usual interstitial pneumonitis or idiopathic pulmonary fibrosis?

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3
Q

What are the symptoms of UIP?

A
  • Dyspnea and/or nonproductive cough
  • Diffuse interstitial infiltrates on chest radiographs
  • Honeycombing on HRCT
  • Restrictive pattern with low DLCO on spirometry
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4
Q

What gender has a worse prognosis in UIP?

A

Males

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5
Q

What is the treatment of UIP?

A

Steroids, lung transplantation.

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6
Q

What is Desquamative Interstitial Pneumonitis (DIP)?

A

DIP is an uncommon ILD. Ninety percent of these patients have a smoking history and present with “smoker’s bronchiolitis.” DIP has a better prognosis than UIP.

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7
Q

What is acute interstitial pneumonitis? What are the symptoms?

A

AIP is another uncommon ILD. It is also called Hamman-Rich syndrome and has a pathologic pattern of diffuse alveolar damage.
Characterized by:
-High fever
-Severe dyspnea over 1 day -Flu-like symptoms
-Rapid respiratory decompensation

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8
Q

What is nonspecific interstitial pneumonia (NSIP) or fibrosis? What is in the differential? What is the prognosis?

A

NSIP is yet another uncommon ILD, which is based on a diagnosis of exclusion. One must rule out collagen vascular disorders, organic dust inhalation, drug reactions, etc. Overall, NSIP has a good prognosis.

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9
Q

What are typical laboratory findings in HP?

A

Increased CD8 in BAL fluid with decreased CD4:CD8

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10
Q

Usual interstitial pneumonia is the typical pathologic pattern in patients with which clinical condition?

A

Idiopathic pulmonary fibrosis

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