What is fibrotic interstitial lung disease?

Published by Charlie Davidson on

What is fibrotic interstitial lung disease?

Interstitial lung disease refers to a group of about 100 chronic lung disorders characterized by inflammation and scarring that make it hard for the lungs to get enough oxygen. The scarring is called pulmonary fibrosis. The symptoms and course of these diseases may vary from person to person.

Does interstitial pneumonitis go away?

There is no cure for ILD. Once scarring happens in the lungs, it usually cannot be reversed. Treatment can help slow the disease down to preserve as much quality of life as possible. The prognosis for patients depends on how severe the condition is, and the cause of the ILD.

What foods should you avoid with pulmonary fibrosis?

Avoid foods that produce mucus, including dairy products (especially ice cream), wheat, corn, cold and raw foods, watermelon, bananas, salty foods, soda, and other sweet foods containing simple processed sugars.

Can you live a long time with interstitial lung disease?

The average survival for people with this type is currently 3 to 5 years . It can be longer with certain medications and depending on its course. People with other types of interstitial lung disease, like sarcoidosis, can live much longer.

Can a fibrotic nonspecific interstitial pneumonia be considered?

In addition to the more classical hypersensitivity pneumonitis, a fibrotic nonspecific interstitial pneumonia should henceforth be considered.

Which is more common NSIP or non-specific pneumonitis?

Fibrotic non-specific interstitial pneumonitis is a histological subtype of non-specific interstitial pneumonitis (NSIP). It is considered the more common form 1 .

How to diagnose nonspecific interstitial pneumonia in women?

Nonspecific interstitial pneumonia is an idiopathic interstitial pneumonia that occurs mainly in women, nonsmokers, and patients < 50 years. Patients have cough and dyspnea, which may be present for months to years. Diagnosis is with high-resolution CT and lung biopsy.

Can a person with NSIP have inflammation and fibrosis?

Both inflammation and fibrosis may be present at the same time. Generally, the prognosis is better for patients with the cellular form of NSIP as inflammation is often reversible but fibrosis is permanent. How common is nonspecific interstitial pneumonia (NSIP)?

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