Lung disease Flashcards
- What are the common themes of interstitial lung diseases?
They all affect the lung parenchyma, pulmonary injury leading to inflammation and fibrosis
- Define idiopathic pulmonary fibrosis (IPF).
Fibrotic lung disease, typically seen in men > 55 years old, unknown cause, may be associated with collagen vascular disease, acid reflux may contribute to disease progression
- What are the symptoms of IPF?
Dry cough and progressive dyspnea, restrictive defect (low Total Lung Capacity), hypoxemia, dx is confirmed by CT, will progress to respiratory failure and death > 50% in 5 years
- Radiology showing “honey-combing” in the periphery of the lung would be indicative of what disease?
IPF
- What are two pathologic processes of IPF?
Usual Interstitial Pneumonia (UIP) and Desquamative Interstitial Pneumonia (DIP)
- What characterizes each of the above processes? Which one is easier to treat?
UIP - extensive fibrosis, and distorted architecture; DIP – alveolar inflammation, macrophages in alveoli, and minimal fibrosis. DIP is easier to treat
- Why is exercise induced hypoxemia a common symptom of IPF?
Thickened, fibrotic tissue between the alveoli and the blood vessels results in inability of oxygen to perfuse across the capillary membrane and be delivered to the tissues
- What are the treatments for IPF?
Corticosteroids, immune suppressive therapy, Nintedanib and Pirfenidone, vaccination for influenza and pneumonia, pulmonary rehab, oxygen, palliative care, and lung transplant
- What is the average survival after lung transplant?
5 years
- What are the main complications after lung transplant?
Infection and rejection
- Define Sarcoidosis.
Chronic granulomatous lung disease of unknown etiology. Can affect many organs, but the lung is most frequently involved
- What are the symptoms of sarcoidosis?
Often asymptomatic, dyspnea, and cough, often spontaneous remission occurs and progression of disease is uncommon
- What is often found on the chest x-ray of people with sarcoidosis?
Symmetrical, and bilateral “Idaho potato” hilar lymph nodes
- What CXR finding characterizes sarcoidosis as Stage II?
Parenchymal tissue involvement
- What CXR finding characterizes sarcoidosis as Stage III?
Lose the enlarged hilar lymph nodes, parenchymal tissue involvement remains
- What is the pathogenesis of sarcoidosis?
Inflammation and activation of T-lymphocytes, formation of granulomas, minimal fibrosis