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Interstitial lung disease

Diffuse parenchymal lung disease; Alveolitis; Idiopathic pulmonary pneumonitis (IPP)

 

Interstitial lung disease is a group of lung disorders in which the lung tissues become inflamed and then damaged.

Causes

 

The lungs contain tiny air sacs (alveoli), which is where oxygen is absorbed. These air sacs expand with each breath.

The tissue around these air sacs is called the interstitium. In people with interstitial lung disease, this tissue becomes stiff or scarred, and the air sacs are not able to expand as much. As a result, not as much oxygen can get to the body.

Interstitial lung disease (ILD) can occur without a known cause. This is called idiopathic ILD. Idiopathic pulmonary fibrosis (IPF) is the most common disease of this type.

There are also dozens of known causes of ILD, including:

  • Autoimmune diseases (in which the immune system attacks the body) such as lupus, rheumatoid arthritis, sarcoidosis, and scleroderma
  • Lung inflammation due to breathing in a foreign substance such as certain types of dust, fungus, or mold (hypersensitivity pneumonitis)
  • Medicines (such as nitrofurantoin, sulfonamides, bleomycin, amiodarone, methotrexate, gold, infliximab, and etanercept)
  • Radiation treatment to the chest
  • Working with or around asbestos, coal dust, cotton dust, and silica dust (called occupational lung disease)

Cigarette smoking may increase the risk of developing some forms of ILD and may cause the disease to be more severe.

 

Symptoms

 

Shortness of breath is a main symptom of interstitial lung disease. You may breathe faster or need to take deep breaths:

  • At first, shortness of breath may not be severe and is only noticed with exercise, climbing stairs, and other activities.
  • Over time, it can occur with less strenuous activity such as bathing or dressing, and as the disease worsens, even with eating or talking.

Most people with this condition also have a dry cough. A dry cough means you do not cough up any mucus or sputum.

Over time, weight loss, fatigue, and muscle and joint pain are also present.

People with more advanced ILD may have:

  • Abnormal enlargement of the base of the fingernails (clubbing)
  • Blue color of the lips, skin, or fingernails due to low blood oxygen levels (cyanosis)
  • Symptoms of the other diseases such as arthritis, associated with ILD

 

Exams and Tests

 

The health care provider will perform a physical exam. Dry, crackling breath sounds may be heard when listening to the chest with a stethoscope.

The following tests may be done:

  • Blood tests to check for autoimmune diseases
  • Bronchoscopy with or without biopsy
  • Chest x-ray
  • CT scan of the chest
  • Echocardiogram 
  • Open lung biopsy
  • Measurement of the blood oxygen level at rest or when active
  • Blood gases
  • Pulmonary function tests
  • Six minute walk test (checks how far you can walk in 6 minutes and how many times you need to stop to catch your breath)

People who are heavily exposed to known causes of lung disease in the workplace are usually routinely screened for lung disease. These jobs include coal mining, sand blasting, and working on a ship.

 

Treatment

 

Treatment depends on the cause of the disease. Medicines that suppress the immune system and reduce swelling in the lungs are prescribed if an autoimmune disease is causing the problem. For some people who have IPF, pirfenidone and nintedanib are two medicines that may be used to slow the disease. If there is no specific treatment for the condition, the aim is to make you more comfortable and support lung function:

  • If you smoke, ask your provider about how to stop smoking.
  • People with low blood oxygen levels will receive oxygen therapy in their home. A respiratory therapist will help you set up the oxygen. Families need to learn proper oxygen storage and safety.

Lung rehabilitation can provide support, and help you learn:

  • Different breathing methods
  • How to set up your home to save energy
  • How to eat enough calories and nutrients
  • How to stay active and strong

Some people with advanced ILD may need a lung transplant.

 

Support Groups

 

You can ease the stress of illness by joining a support group. Sharing with others who have common experiences and problems can help you not feel alone.

 

Outlook (Prognosis)

 

The chance of recovering or ILD getting worse depends on the cause and how severe the disease was when it was first diagnosed.

Some people with ILD develop heart failure and high blood pressure in the blood vessels of their lungs.

Idiopathic pulmonary fibrosis has a poor outlook.

 

When to Contact a Medical Professional

 

Call your provider if:

  • Your breathing is getting harder, faster, or more shallow than before
  • You cannot get a deep breath, or need to lean forward when sitting
  • You are having headaches more often
  • You feel sleepy or confused
  • You have a fever
  • You are coughing up dark mucus
  • Your fingertips or the skin around your fingernails is blue

 

 

References

Raghu G. Interstitial lung disease. In: Goldman L, Schafer AI, eds. Goldman's Cecil Medicine. 25th ed. Philadelphia, PA: Elsevier Saunders; 2016:chap 92.

Ryu JH, Selman M, Colby TV, King TE. Idiopathic interstitial pneumonias. In: Broaddus VC, Mason RJ, Ernst JD, et al, eds. Murray and Nadel's Textbook of Respiratory Medicine. 6th ed. Philadelphia, PA: Elsevier Saunders; 2016:chap 63.

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    Clubbing

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  • Coal workers pneumoconiosis - stage II

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  • Coal workers pneumoconiosis - stage II #2

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  • Coal workers pneumoconiosis, complicated

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  • Respiratory system

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    • Clubbing

      Clubbing

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    • Coal workers pneumoconiosis - stage II

      Coal workers pneumoconio...

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    • Coal workers pneumoconiosis - stage II #2

      Coal workers pneumoconio...

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    • Coal workers pneumoconiosis, complicated

      Coal workers pneumoconio...

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    A Closer Look

     

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        Tests for Interstitial lung disease

         
         

        Review Date: 11/19/2015

        Reviewed By: Denis Hadjiliadis, MD, MHS, Associate Professor of Medicine, Pulmonary, Allergy, and Critical Care, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA. Also reviewed by David Zieve, MD, MHA, Isla Ogilvie, PhD, and the A.D.A.M. Editorial team.

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