Tracheobronchomegaly: Difference between revisions
CSV import |
CSV import |
||
| Line 32: | Line 32: | ||
* [https://rarediseases.info.nih.gov/diseases/7831/tracheobronchomegaly Tracheobronchomegaly] at [[National Organization for Rare Disorders]] | * [https://rarediseases.info.nih.gov/diseases/7831/tracheobronchomegaly Tracheobronchomegaly] at [[National Organization for Rare Disorders]] | ||
__NOINDEX__ | __NOINDEX__ | ||
{{No image}} | |||
Revision as of 04:05, 11 February 2025
Tracheobronchomegaly is a rare disease characterized by an abnormal enlargement of the trachea and the bronchi of the lungs. This condition is also known as Mounier-Kuhn syndrome, named after the physicians who first described it.
Symptoms
The symptoms of Tracheobronchomegaly can vary greatly from person to person. Some individuals may have no symptoms at all, while others may experience severe respiratory problems. Common symptoms include chronic cough, recurrent respiratory infections, and shortness of breath.
Causes
The exact cause of Tracheobronchomegaly is unknown. However, it is believed to be due to a defect in the elastic tissue of the trachea and bronchi. This defect causes the airways to become weak and dilated, leading to the symptoms of the disease.
Diagnosis
Diagnosis of Tracheobronchomegaly is typically made through imaging studies such as chest X-ray or computed tomography (CT) scan. These tests can show the enlarged trachea and bronchi. In some cases, a bronchoscopy may also be performed to examine the airways.
Treatment
There is currently no cure for Tracheobronchomegaly. Treatment is focused on managing the symptoms and preventing complications. This may include antibiotics to treat respiratory infections, bronchodilators to open the airways, and physiotherapy to improve lung function.
