Causes of Pulmonary fibrosis
List of causes of Pulmonary fibrosis
Following is a list of causes or underlying conditions
(see also Misdiagnosis of underlying causes of Pulmonary fibrosis)
that could possibly cause Pulmonary fibrosis includes:
Causes of Pulmonary fibrosis (Diseases Database):
The follow list shows some of the possible medical causes of Pulmonary fibrosis
that are listed by the Diseases Database:
Source: Diseases Database
Pulmonary fibrosis Causes: Book Excerpts
Pulmonary fibrosis as a complication of other conditions:
Other conditions that might have
Pulmonary fibrosis as a complication may,
potentially, be an underlying cause of Pulmonary fibrosis.
Our database lists the following as having
Pulmonary fibrosis as a complication of that condition:
Pulmonary fibrosis as a symptom:
Conditions listing Pulmonary fibrosis
as a symptom may also be potential underlying causes of Pulmonary fibrosis.
Our database lists the following as having
Pulmonary fibrosis as a symptom of that condition:
Medications or substances causing Pulmonary fibrosis:
The following drugs, medications, substances or toxins are some of the possible
causes of Pulmonary fibrosis as a symptom.
This list is incomplete and various other drugs or substances
may cause your symptoms.
Always advise your doctor of any medications or treatments you are using,
including prescription, over-the-counter, supplements, herbal or alternative treatments.
Read more about medication causes of Pulmonary fibrosis
Related information on causes of Pulmonary fibrosis:
As with all medical conditions,
there may be many causal factors.
Further relevant information on causes of Pulmonary fibrosis may be found in:
Causes of Pulmonary fibrosis: Online Medical Books
16 MEDICAL BOOKS ONLINE!
Review excerpts from medical books online, free, without registration,
for more information about the causes of Pulmonary fibrosis.
Idiopathic pulmonary fibrosis:
Causes and incidence
(Professional Guide to Diseases (Eighth Edition))
IPF is the result of a cascade of events that involve inflammatory, immune, and fibrotic processes in the lung. However, despite many studies and hypotheses, the stimulus that begins the progression remains unknown. Speculation has revolved around viral and genetic causes, but no good evidence has been found to support either theory. However, it’s clear that chronic inflammation plays an important role. Inflammation develops the injury and the fibrosis that ultimately distorts and impairs the structure and function of the alveolocapillary gas exchange surface.
IPF is slightly more common in men than in women and is more common in smokers than in nonsmokers. It usually affects people ages 50 to 70.
» READ BOOK EXCERPT ONLINE »
Source: Professional Guide to Diseases (Eighth Edition), 2005
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