Restrictive Lung Disease-Bootcamp Flashcards
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Idiopathic pulmonary fibrosis is _
Idiopathic pulmonary fibrosis is slow onset of fibrotic deposition in the lungs of unknown etiology
Common symptoms of IPF include:
Common symptoms of IPF include: dyspnea, non-productive cough, fatigue, crackles
_ imaging is often used for the diagnosis of IPF in which _ and _ will be observed
CXR/CT imaging is often used for the diagnosis of IPF in which bilateral diffuse reticulonodular opacities and honeycombing will be observed
* Looks like a net-like pattern of nodular fibrosis
Explain the pathogenesis of IPF
IPF involves repetitive injury, followed by disorganized repair
The repetitive injuries that might lead to IPF include things like _ or _
The repetitive injuries that might lead to IPF include things like smoking or acid reflux
Explain how the repair process of the lungs becomes disorganized in IPF
Type 1 pneumocytes are injured + abnormal BM –>
Type 2 pneumocytes will try to regenerate them –> Hyperplasia with failed differentiation (due to abnormal BM) –>
Impaired re-epithelialization causes fibroblasts to undergo focal proliferation and lay down collagen –>
Fibrotic lungs
When a known chemical or radiation causes damage to the lung resulting in scarring and fibrosis, we call this _
When a known chemical or radiation causes damage to the lung resulting in scarring and fibrosis, we call this drugs and radiation-induced fibrosis
* This is not considered IPF because it has known cause
Four drugs commonly associated with lung fibrosis
- Bleomycin
- Amiodarone
- Methotrexate
- Busulfan
For the first 12 weeks post radiation the effect on the lung is _
For the first 12 weeks post radiation the effect on the lung is neumonitis (inflammation)
Fibrosis can occur _ months after radiation
Fibrosis can occur 6-12 months after radiation
In order for Type II pneumocytes to regenerate Type I pneumocytes there must be presense of _
In order for Type II pneumocytes to regenerate Type I pneumocytes there must be presense of normal basement membrane
What is pneumoconiosis?
Pneumoconiosis is an occupationally acquired restrictive lung disease that occurs after many years of inhaling dust particles
Pneumoconiosis pathogenesis begins with dust particles inhaled –> ?
Dust particles inhaled into alveoli –> Alveolar macrophages phagocytose dust –> Trigger cytokine release –> Activation of fibroblasts –> Fibrosis
Blackened “carbon-laden” macrophages in the upper lungs is called _ and is associated with _
Blackened “carbon-laden” macrophages in the upper lungs is called anthracosis and is associated with coal-miner’s pneumoconiosis
_ pneumoconiosis is associated with an increased risk of TB infection
Silicosis is associated with an increased risk of TB infection
* Silicosis causes macrophage dysfunction