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Overview of Idiopathic Interstitial Pneumonias


Joyce Lee

, MD, MAS, University of Colorado Denver

Last full review/revision Sep 2019| Content last modified Sep 2019
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Idiopathic interstitial pneumonias are interstitial lung diseases that have no known cause that have some similarities in symptoms and how they affect the lungs.

  • Some types of these diseases are much more serious than others.

  • Diagnosis requires chest x-rays, computed tomography, and usually analysis of a sample of lung tissue (biopsy).

  • Treatment depends on the disease type.

The word idiopathic means of unknown cause, so when the cause of interstitial lung disease is not identified, idiopathic interstitial pneumonia is diagnosed. Pneumonias are often thought of as infections, but these diseases do not appear to result from infection.

There are eight types of idiopathic interstitial pneumonias. In decreasing order of frequency, they are

All types cause cough and shortness of breath and affect the lungs similarly. The ends of the fingers may become thick or club-shaped (see figure Recognizing Finger Clubbing). Through a stethoscope, doctors often hear crackling sounds. Although symptoms may be similar, disorders differ in how quickly symptoms develop, how they are treated, and how serious they are.


Comparing Types Of Idiopathic Interstitial Pneumonias*


People Most Often Affected

Percentage of Affected People Who Smoke Cigarettes



Idiopathic pulmonary fibrosis

More frequently, men over 50

More than 60%

Pulmonary rehabilitation

Lung transplantation

Pirfenidone or nintedanib

50–70% die in 5 years.

Desquamative interstitial pneumonia

More frequently, men aged 30–50

More than 90%

Smoking cessation


5% die in 5 years.

Nonspecific interstitial pneumonia

More frequently, women aged 40–60

Fewer than 40%


Fewer than 50% die in 5 years.

Cryptogenic organizing pneumonia

People of any age, usually aged 40–50

Fewer than 50%


Two thirds completely recover, but the disorder recurs in many.

Death is rare.

Respiratory bronchiolitis–associated interstitial lung disease

People aged 30–50 (slightly more men)

More than 90%

Smoking cessation


Death is rare.

Acute interstitial pneumonia

People of any age


Best treatment unknown

60% die in less than 6 months.

Lymphoid interstitial pneumonia

Mostly women of any age



The prognosis is difficult to predict.

Idiopathic pleuroparenchymal fibroelastosis

People of any age (median age 57)

Usually non-smokers

Best treatment unknown (possibly corticosteroids)

Disease progresses in 60% of people.

* In decreasing order of frequency.


  • Chest x-rays and chest computed tomography

Chest x-rays are done. Computed tomography (CT) of the chest is also done. CT may allow doctors to make a diagnosis. If not, doctors remove a small sample of lung tissue for examination under a microscope (lung biopsy). Usually, biopsy is done surgically with use of a thoracoscope.

Blood tests are usually done. They usually cannot confirm the diagnosis but are done as part of the search for other disorders. Doctors may also do electrocardiography (ECG) or echocardiography to determine whether the heart has been affected by the lung disease.


  • Smoking cessation

  • Often drugs, corticosteroids or novel antifibrotic drugs, depending on the disease

  • Sometimes lung transplantation

Smoking cessation is always recommended because smoking is likely to make the disorder progress more rapidly.

Other treatments depend on the type of idiopathic interstitial pneumonia but may include corticosteroids or other drugs, such as novel antifibrotic drugs.

In some people, lung transplantation is done.

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