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Fibrosis of the lungs — also known as pulmonary fibrosis — is a condition where the lung tissue becomes thick, stiff, and scarred over time. This scarring makes it harder for the lungs to expand and for oxygen to move into the bloodstream. Patients often first notice breathlessness, dry cough, or fatigue, but the underlying damage usually begins long before symptoms appear.
At Sai Hospital, Haldwani, our pulmonologists regularly diagnose and manage lung fibrosis, helping patients understand the cause, control symptoms, and slow the condition’s progression. This detailed guide explains what causes fibrosis of the lungs, who is at risk, and what early signs should not be ignored.
Lung fibrosis refers to scarring of lung tissue, particularly the interstitium — the thin, delicate lining between the air sacs. When this tissue becomes scarred, the lungs become less flexible and cannot transfer oxygen efficiently.
Fibrosis can be idiopathic (cause unknown) or due to identifiable triggers such as infections, long-term inflammation, environmental exposure, medications, or autoimmune diseases.
There is no single cause. Lung fibrosis can develop due to several factors, and sometimes multiple causes overlap. Below are the most important contributors.
This is the most common type of lung fibrosis, and sadly, the cause is still unknown.
“Idiopathic” means doctors cannot identify a specific reason.
However, contributing factors may include:
IPF mainly affects adults over 50 and progresses gradually.
Repeated inhalation of harmful particles can irritate and damage lung tissue over time.
Workers in construction, textile, carpentry, welding, mining, and agriculture are particularly at risk.
This category includes diseases like:
Several autoimmune diseases can attack the lungs, causing inflammation that eventually leads to scarring.
When the immune system mistakenly attacks lung tissue, fibrosis may develop gradually.
Chronic infections or inflammatory lung diseases can damage the interstitium.
Examples include:
If inflammation continues, the healing response forms scar tissue instead of normal lung tissue.
Some medicines, especially when taken long-term or in high doses, can cause lung scarring.
Doctors monitor lung function closely in patients using these drugs.
Smoking is one of the strongest risk factors for developing lung fibrosis.
It damages the air sacs, weakens lung immunity, and triggers abnormal healing responses. Even passive smoking increases the risk.
Certain viral infections can damage lung tissue and lead to fibrosis, especially if the inflammation is severe or long-lasting.
COVID-19 has been a major contributor to new fibrosis cases worldwide due to severe lung inflammation in some patients.
In some families, fibrosis runs in the genes.
Genetic abnormalities can affect how lung tissue repairs itself, causing scar formation even after minor injuries.
Conditions like familial pulmonary fibrosis are well-recognized.
Repeated micro-aspiration of stomach acid into the lungs — often unnoticed — can irritate lung tissue and contribute to scarring. This is more common in people with severe or uncontrolled reflux disease.
As people age, lung tissue becomes more vulnerable to injury.
Older adults also have slower tissue repair, making them more prone to fibrosis even with mild irritants.
Many patients ignore early signs, assuming it’s just aging or reduced stamina.
But early detection makes a significant difference.
If you notice these for more than a few weeks, a lung evaluation is important.
At Sai Hospital, Haldwani, pulmonologists use a combination of tests:
Accurate diagnosis helps identify the cause and guide treatment.
Lung fibrosis cannot be completely reversed because scar tissue does not turn back into normal lung tissue.
However, early diagnosis and treatment slow the progression, reduce symptoms, and improve quality of life.
1. Can lung fibrosis be caused by COVID-19?
Yes. Severe COVID-19 pneumonia can lead to scarring in some patients.
2. Can smoking alone cause lung fibrosis?
Yes. Smoking damages lung tissue and significantly increases fibrosis risk.
3. Is fibrosis hereditary?
In some families, genetic mutations can cause inherited pulmonary fibrosis.
4. Does dust exposure cause fibrosis?
Long-term exposure to silica, asbestos, or coal dust is a common cause.
5. Can fibrosis be stopped from worsening?
With early diagnosis, medications and lifestyle changes can slow progression.
So, what causes fibrosis of the lungs?
The reasons range from autoimmune diseases to environmental exposures, medication effects, chronic inflammation, infections, smoking, and even unknown causes like idiopathic pulmonary fibrosis.
At Sai Hospital, Haldwani, our pulmonologists focus on early detection, personalized treatment, and long-term management to help patients breathe better and live healthier lives.
If you or someone you know is experiencing persistent breathlessness or chronic cough, don’t ignore it — early evaluation can prevent long-term damage.