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Condition characterized by fibrosis of the lungs and an increase in size of the alveolar chambers?
Wiki User
∙ 12y ago
Emphysema generally is characterized by such symptoms, as well as:
- Patients becoming barrel-chested due to air retention
- Alveolar wall destruction
- Chronic lung inflammation
- Loss of lung elasticity
- Collapse of bronchioles on expiration
As well as those already stated!
Wiki User
∙ 12y ago
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What is condition with fibrosis of the lungs and increased size of alveolar chambers?
The medical condition surrounding the diagnostic criteria of fibrosis of the lungs and increased alveolar chamber size is known as emphysema, which is included in a group of respiratory diseases called chronic obstructive pulmonary diseases (COPD).
Scar tissue that replaces the pulmonary alveolar walls is known as pulmonary?
fibrosis
Are lingular and pulmonary fibrosis the same?
No, lingular and pulmonary fibrosis are not the same. Pulmonary fibrosis is a condition where the lung tissue becomes thick and stiff, and the air sacs of the lungs become scarred. This can cause difficulty breathing, coughing, and chest pain. Lingular fibrosis is a specific type of pulmonary fibrosis. It is a form of idiopathic interstitial pneumonia and affects the middle lobe of the lung. It is more common in women than in men and is seen in people who are between the ages of 40 and 70. Pulmonary fibrosis is a progressive and often fatal condition that is caused by an unknown etiology and is characterized by scarring of the lung tissue. This scarring can cause the tissue to become thick and stiff, which can make it difficult for air to move in and out of the lungs, leading to shortness of breath and other respiratory symptoms. Common causes of pulmonary fibrosis include environmental exposures, medications, radiation therapy, and autoimmune conditions. Lingular fibrosis is a form of idiopathic interstitial pneumonia that affects the middle lobe of the lung. It is more common in women than in men, and is seen in people who are between the ages of 40 and 70. The cause of lingular fibrosis is unknown, but it is thought to be related to an autoimmune condition. It is characterized by scarring of the lung tissue, and can cause difficulty breathing, coughing, and chest pain. The symptoms of both pulmonary fibrosis and lingular fibrosis are similar, but the two conditions are distinct. Pulmonary fibrosis affects the entire lung, while lingular fibrosis only affects the middle lobe. In addition, the causes of the two conditions are different. While the cause of pulmonary fibrosis is unknown, lingular fibrosis is thought to be related to an autoimmune condition. Therefore, lingular and pulmonary fibrosis are not the same.
is biapical focal fibrosis the same as pulmonary fibrosis?
No, biapical focal fibrosis is not the same as pulmonary fibrosis. Pulmonary fibrosis is a general term used to describe a group of conditions that cause scarring of the lung tissue. It is a progressive, long-term condition that can eventually lead to respiratory failure. Pulmonary fibrosis can be caused by a variety of factors, including environmental exposures, some medications, or underlying medical conditions. Biapical focal fibrosis is a specific type of pulmonary fibrosis. It is characterized by localized scarring of the lung tissue in two different areas of the lung, the apex and the base. This condition is more common in women and is often caused by an autoimmune response. Biapical focal fibrosis can be difficult to diagnose due to the localized nature of the scarring, but it can be identified through a combination of physical exam, imaging, and laboratory tests. Treatment options are limited and typically involve corticosteroids to reduce inflammation and other medications to slow the progression of the disease. In summary, biapical focal fibrosis is not the same as pulmonary fibrosis. While pulmonary fibrosis is a general term used to describe a group of lung diseases, biapical focal fibrosis is a specific type of pulmonary fibrosis characterized by localized scarring in two different areas of the lung.
What environmental conditions may cause damage to the alveolar sacs?
Coal dust, silica dust, and asbestos, which may lead to pulmonary fibrosis
Is cystic fibrosis caused by a pathogen?
No, cystic fibrosis is a genetic condition. Both parents carry the gene.
What is the most common lethal genetic disease in US African Americans?
Cystic fibrosis it is characterized by thick mucus in the lungs
What does pneumoconiosis mean?
a disease of the lungs due to inhalation of dust, characterized by inflammation, coughing, and fibrosis.
What vector is used for Cystic fibrosis?
If by vector you mean the organism which causes it, there is none. Cystic fibrosis is a genetic condition.
In which city is the Cystic Fibrosis foundation located?
The Cystic Fibrosis Foundation has headquarters located in Bethesda in Maryland. This is a charity which supports sufferers of cystic fibrosis, a hereditary condition.
What would be an example of deletion mutation disease?
Cystic fibrosis: characterized by abnormally thick mucus in the lungs, intestines, and pancreas
What is residual fibrosis in lungs?
Residual fibrosis in the lungs is scarring. The condition is not hereditary and can be caused by an infection or by a previous illness involving the lungs.
