Bronchiectasis is an abnormal stretching and enlarging of the respiratory
passages caused by mucus blockage. When the body is unable to get rid of
mucus, mucus becomes stuck and accumulates in the airways. The blockage and
accompanying infection cause inflammation, leading to the weakening and
widening of the passages. The weakened passages can become scarred and
deformed, allowing more mucus and bacteria to accumulate, resulting in a
cycle of infection and blocked airways.
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Bronchiectasis is one of the chronic obstructive pulmonary diseases
COPD )* and
it can be complicated by emphysema
and
bronchitis. The disease is commonly misdiagnosed as asthma or pneumonia.
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Bronchiectasis can develop at any age, begins most often in childhood,
but symptoms may not be apparent until much later. Bronchiectasis can
occur as part of a birth defect, such as primary ciliary's dyskinesia
or
cystic fibrosis. About 50% of all cases of bronchiectasis in the U.S.
result from cystic fibrosis. It can also develop after birth as a result
of injury or other diseases, like tuberculosis, pneumonia and
influenza.
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There
are three types of bronchiectasis that describe the severity of the
condition:
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Cylindrical - most common and refers to the slight widening of the
respiratory passages. This type can be reversed and may be seen after
acute bronchitis.
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Varicose - bronchial walls have both extended and collapsed portions.
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Cystic - most severe and involves irreversible ballooning of the
bronchi.
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Symptoms include coughing (worsened when lying down), shortness of
breath, abnormal chest sounds, weakness, weight loss, and fatigue. With
infections the mucus may be discolored, foul smelling and may contain
blood. Symptom severity varies widely from patient to patient and
occasionally, a patient is asymptomatic.
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Doctors evaluate bronchiectasis with a chest x-ray, breathing tests,
sputum culture or computed tomography (CT) scan. Testing for other
associated diseases like cystic fibrosis or tuberculosis can also be
helpful.
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Bronchiectasis patients are often given antibiotics for infection and
bronchodilator medicines to open passages. There are also physical
therapy techniques to help clear mucus. Lung transplants are also an
option for severe cases. Fatalities are uncommon but may result from
massive hemorrhage.
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If
lung infections are treated immediately, bronchiectasis is less likely
to develop. Bronchiectasis patients should avoid cigarette smoke and
other irritants and refrain from using sedatives. Vaccinations against
measles, influenza and other infections could also be a good
preventative measure.
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