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Asthma & Other Lung Diseases

Also called: Asthma Related Breathing Problems

- Summary
- About asthma and lung disease
- About COPD
- About cardiac asthma
- About bronchitis
- About immotile cilia syndrome
- About foreign bodies
- About bronchiectasis
- About cystic fibrosis
- About vocal cord dysfunction
- About congenital heart disease
- About bronchopulmonary dysplasia
- About primary immunodeficiency
- Questions for your doctor

Reviewed By:
Norman Klein, M.D., FAAAAI

About bronchiectasis

Bronchiectasis is damage to the bronchial tubes caused by repeated infections.Bronchiectasis is damage to the bronchial tubes caused by repeated infections.  It involves the production of very thick, green mucus that obstructs the bronchial tubes. This leads to abnormal stretching and enlarging of the respiratory passage. Symptoms may include:

  • Wheezing

  • Repeated bouts of bronchitis and pneumonia

  • A cough that is:
    • Persistent with large amounts of foul-smelling sputum
    • Accompanied by blood
    • Worsened by lying on one's side

  • Shortness of breath worsened by exercise

  • Weight loss

  • Fatigue

  • Weakness

  • Clubbing of the fingers (abnormal amounts of tissue in the nail beds)

  • Paleness

  • Foul-smelling breath

  • Bluish skin discoloration (cyanosis)

The disease is often misdiagnosed as asthma or pneumonia. It often develops in childhood, but symptoms may not appear until much later in life. The condition can result from a birth defect (e.g., cystic fibrosis) or develop after birth due to injury, or disease (e.g., tuberculosis, pneumonia, influenza).

A standard chest x-ray often will reveal the condition. Sometimes, high–resolution computed axial tomography (CAT scan) is necessary to confirm the diagnosis and determine the extent of the disease. A sputum culture and other tests may also be used. 

 

Bronchodilators, antibiotics and corticosteroids may be used to treat flare-ups. Physical therapy can also benefit the patient by teaching them techniques to help clear the mucus. In severe cases, a lung transplant may be considered.

About cystic fibrosis

Cystic fibrosis is a hereditary disease that causes glands to produce abnormal secretions that block the airways, leading to significant breathing problems. A form of intestinal obstruction called meconium ileus afflicts a minority of newborns diagnosed with cystic fibrosis. For others, poor weight gain is likely to be the first symptom of cystic fibrosis.

Other symptoms may include:

  • Frequent, bulky, foul-smelling stools
  • Protruding abdomen
  • Slow growth
  • Coughing
  • Wheezing
  • Shortness of breath
  • Recurrent respiratory infections (e.g., pneumonia, sinusitis)
  • Gagging and vomiting
  • Disturbed sleep
  • Excessive appetite
  • Diarrhea
  • Greasy stools
  • Fatigue
  • Loss of smell associated with nasal polyps
  • Salty tasting skin

 

Several tests are used to diagnose this condition, including digestive enzyme trypsin analysis (high levels of this enzyme indicate the presence of cystic fibrosis), quantitative pilocarpine iontophoresis sweat test (measures the amount of salt in sweat) and stool analysis.

 

Treatment for lung problems associated with the disease includes routine vaccinations and influenza shots (viral infections increase lung damage). Patients may also benefit from regular sessions with a respiratory therapist who can teach them techniques to help clear mucus. Bronchodilators, antibiotics and other drugs may also be prescribed.

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Review Date: 06-21-2007

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