Best Pulmonary Fibrosis Clinics in Warsaw: Where to Go for Diagnosis and Treatment

Finding the right specialist centre can matter when pulmonary fibrosis or another interstitial lung disease (ILD) is suspected. These conditions can look similar on symptoms alone, while their causes and medical management can differ.

Warsaw has several specialist services with documented expertise in pulmonary fibrosis, idiopathic pulmonary fibrosis (IPF), progressive pulmonary fibrosis (PPF), autoimmune-related ILD, advanced respiratory diagnostics, and lung transplantation.

The centres below are not ranked from best to worst. “Best” reflects search intent rather than a clinical league table. Each service has a different focus, so the most relevant option depends on the type of ILD being investigated, the expertise required, referral arrangements, and discussions with your healthcare team.

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Why can a specialist pulmonary fibrosis clinic be useful?

A specialist pulmonary fibrosis clinic can bring together the expertise needed to distinguish between different forms of ILD and decide which further investigations are appropriate.

Pulmonary fibrosis describes scarring of lung tissue rather than one single disease. Idiopathic pulmonary fibrosis is one specific form. Fibrosis can also occur with autoimmune or connective-tissue diseases, hypersensitivity pneumonitis, occupational exposures, medicines, and other ILDs.

International guidelines emphasize high-resolution CT imaging and multidisciplinary discussion when IPF is being considered. Depending on the findings, specialists from pulmonology, thoracic radiology, pathology, or rheumatology may contribute. Not everyone requires an invasive test or lung biopsy.

For an introduction to the condition, read mama health's guide to pulmonary fibrosis.

Which pulmonary fibrosis clinics in Warsaw have specialist ILD expertise?

Warsaw has five particularly relevant specialist services when pulmonary fibrosis or another fibrosing ILD is being investigated or managed.

Some are separate centres, while others are specialist clinics within the same larger hospital. Their roles are not identical, which is important when choosing where to enquire.

1. PIM MSWiA Centre for the Diagnosis and Treatment of Pulmonary Fibrosis

The Państwowy Instytut Medyczny MSWiA has one of Warsaw's most specifically focused services for pulmonary fibrosis.

In November 2025, PIM MSWiA announced a dedicated Centre for the Diagnosis and Treatment of Pulmonary Fibrosis. The centre brings pulmonology, rheumatology, and cardiac surgery expertise together for fibrosing interstitial lung diseases.

Its pulmonology service explicitly covers idiopathic pulmonary fibrosis, hypersensitivity pneumonitis, connective-tissue-disease-associated ILD, and other interstitial lung diseases. Available respiratory investigations include HRCT, spirometry, plethysmography, DLCO, the six-minute walk test, bronchoscopy, EBUS, and lung biopsy techniques where medically appropriate.

The clinic currently lists the Polish B.87 programme for idiopathic pulmonary fibrosis and B.135 programme for progressive pulmonary fibrosis. It also provides preliminary assessment for lung transplantation. Eligibility for any programme or procedure is determined by the specialist team under current clinical and reimbursement criteria.

Location: ul. Wołoska 137, 02-507 Warsaw

Why consider it: a dedicated pulmonary fibrosis centre, broad ILD diagnostics, multidisciplinary expertise, fibrosis-specific drug programmes, and lung transplant expertise.

2. First Department of Lung Diseases, Institute of Tuberculosis and Lung Diseases

The First Department of Lung Diseases at the Institute of Tuberculosis and Lung Diseases has a dedicated clinical focus on interstitial lung diseases and all forms of pulmonary fibrosis.

Its published areas of expertise include pulmonary fibrosis, sarcoidosis, hypersensitivity pneumonitis, other interstitial pneumonias, and lung involvement associated with connective-tissue diseases.

The wider institute has specialist radiology, respiratory physiology, pathology, immunology, genetics, and endoscopic diagnostics. Its pathology service specifically describes expertise in interstitial lung disease and IPF.

The institute also states that its doctors have contributed to diagnostic and therapeutic standards for IPF and that it participates in the European EMPIRE IPF registry. Its pulmonary fibrosis services include the B.87 IPF programme.

Location: ul. Płocka 26, 01-138 Warsaw

Why consider it: extensive ILD experience, access to multiple diagnostic specialties within one lung institute, and longstanding academic involvement in IPF.

3. Third Department of Lung Diseases, Institute of Tuberculosis and Lung Diseases

The Third Department of Lung Diseases at the same Warsaw institute has a particularly strong focus on rare ILDs, IPF, and other progressively fibrosing lung diseases.

The department explicitly lists idiopathic pulmonary fibrosis, hypersensitivity pneumonitis, sarcoidosis, organizing pneumonia, connective-tissue-disease-related lung involvement, and other interstitial pneumonias, including forms with progressive fibrosis.

It currently lists both the B.87 IPF programme and B.135 programme for other ILDs with progressive pulmonary fibrosis. The department also participates in research involving interstitial and rare lung diseases.

Although this department and the First Department are part of the same institution, listing them separately is useful because both explicitly describe ILD as a major area of specialist work.

Location: ul. Płocka 26, 01-138 Warsaw

Why consider it: specialist IPF and progressive-fibrosis expertise, rare lung disease experience, and access to fibrosis-specific drug programmes.

4. Wojskowy Instytut Medyczny – PIB

The pulmonary service at the Military Institute of Medicine provides specialist respiratory care and currently lists a programme for idiopathic pulmonary fibrosis.

Its Clinic of Internal Medicine, Pneumonology, Allergology, Clinical Immunology and Rare Diseases operates a specialist pulmonary outpatient service and a home oxygen service. The clinic's official information lists an IPF drug programme among its current areas of care.

The wider institute can also be relevant when pulmonary fibrosis occurs alongside autoimmune disease. Its rheumatology department assesses pulmonary complications associated with chronic inflammatory joint disease, and WIM continues to conduct research involving systemic-sclerosis-associated ILD.

Location: ul. Szaserów 128, 04-141 Warsaw

Why consider it: specialist pulmonology, an IPF programme, home oxygen services, and access to rheumatology expertise when autoimmune disease is relevant.

5. UCK WUM Rheumatology Clinic

The Rheumatology Clinic at the University Clinical Centre of the Medical University of Warsaw is particularly relevant for fibrosing ILD associated with systemic autoimmune and connective-tissue diseases.

In 2026, UCK WUM announced participation in the B.135 programme for interstitial lung diseases, specifically including systemic-sclerosis-associated ILD and progressive fibrosing ILD related to systemic connective-tissue diseases.

This is an important distinction. The service is not presented as a general IPF clinic. Its particular relevance is when lung fibrosis occurs alongside conditions such as systemic sclerosis or another systemic rheumatic disease.

Location: Przychodnia Specjalistyczna Lindleya, ul. Lindleya 4, 02-005 Warsaw.

Why consider it: specific expertise in autoimmune-associated ILD and access to the B.135 programme for eligible forms of progressive fibrosing ILD.

Where can you start if pulmonary fibrosis has not been confirmed yet?

A respiratory centre that explicitly specializes in ILD can be a useful starting point when the exact diagnosis is still uncertain.

Pulmonary fibrosis can have different causes, so an initial assessment may involve more than confirming that fibrosis exists on a scan. Specialists may review medical history, previous imaging, medicines, occupational and environmental exposures, autoimmune symptoms, lung-function results, and other investigations.

For suspected IPF, guidelines emphasize excluding known causes of ILD and reviewing HRCT findings. Multidisciplinary discussion can be particularly useful when the imaging or clinical picture is not straightforward.

In Warsaw, the Institute of Tuberculosis and Lung Diseases and PIM MSWiA both explicitly describe broad ILD diagnostic services. If an autoimmune or rheumatic disease is already part of the picture, services with combined pulmonology and rheumatology expertise may also be relevant to discuss with your healthcare team.

For more background before an appointment, see mama health's guide to common signs and symptoms associated with pulmonary fibrosis.

What tests might a pulmonary fibrosis clinic use?

ILD assessment commonly combines imaging, lung-function testing, medical history, and selected additional investigations rather than relying on one test alone.

HRCT is central to the assessment of suspected IPF because it can identify radiological patterns such as usual interstitial pneumonia. Pulmonary function tests can provide information about lung volumes and gas transfer, often including FVC and DLCO.

Depending on the clinical question, a specialist centre may also consider blood tests, exercise testing, bronchoscopy, bronchoalveolar lavage, cryobiopsy, or other tissue sampling. These tests are not automatically required for everyone. Guidelines specifically advise against routine surgical lung biopsy in some situations where the HRCT pattern and clinical context already provide sufficient diagnostic information.

When another cause is possible, the assessment may also look at autoimmune disease, medicines, occupational exposures, birds, mould, dust, chemicals, or other environmental factors.

If you want to understand how IPF fits within the broader group of fibrosing lung diseases, read mama health's guide to how idiopathic pulmonary fibrosis differs from other forms.

What pulmonary fibrosis treatments are available through Warsaw specialist centres?

Treatment depends on the type of pulmonary fibrosis rather than fibrosis being treated as one single disease.

Several Warsaw centres currently list national drug programmes for IPF or other forms of progressive pulmonary fibrosis. The Institute of Tuberculosis and Lung Diseases and PIM MSWiA list B.87 for IPF, while specialist services at PIM MSWiA, the Institute of Tuberculosis and Lung Diseases, and UCK WUM also describe B.135 pathways for eligible progressive fibrosing ILDs.

Other aspects of specialist care can include pulmonary rehabilitation, oxygen therapy where clinically indicated, management of associated conditions, and assessment for lung transplantation in selected situations. What is appropriate varies considerably according to the ILD subtype, lung function, other health conditions, and specialist assessment.

Current drug programmes and eligibility rules can change. Confirm the current pathway directly with the centre rather than assuming that a particular medicine or programme applies to your situation.

How should you choose between pulmonary fibrosis clinics in Warsaw?

The most useful clinic is usually the one whose specialist focus matches the medical question that needs to be answered.

If the diagnosis remains uncertain, look for broad ILD expertise and access to HRCT review, pulmonary function testing, and multidisciplinary assessment. If IPF has already been identified, you may want to ask whether the centre currently provides the relevant national drug programme. If fibrosis is connected with systemic sclerosis, rheumatoid arthritis, or another autoimmune disease, access to rheumatology expertise may be particularly relevant.

For more advanced lung disease, it can also be useful to know whether the centre provides respiratory rehabilitation, oxygen services, or transplant assessment.

Before arranging a visit, confirm the current referral rules, appointment pathway, and what documentation the clinic wants to receive. Services and eligibility criteria can change.

What should you bring to a pulmonary fibrosis appointment in Warsaw?

Bringing an organized medical history can make it easier to explain what has happened so far and use appointment time effectively.

Useful information can include previous CT scans and the original image files where available, radiology reports, spirometry and DLCO results, hospital discharge summaries, current and previous prescriptions, relevant laboratory results, autoimmune or rheumatology investigations, previous bronchoscopy or pathology reports, and information about work or environmental exposures.

It can also help to write down changes you want to remember, such as when breathlessness occurs, whether cough has changed, how daily activities have been affected, and any questions that have accumulated since the last appointment.

The clinics themselves may have specific requirements. For example, PIM MSWiA asks those attending its pulmonary outpatient service to bring previous investigation results, discharge records, respiratory imaging, and a list of diagnoses and medicines. The Institute of Tuberculosis and Lung Diseases also publishes specific registration and documentation requirements for its outpatient service.

What can the experience of others with pulmonary fibrosis add?

What others have experienced can help surface practical questions that may not appear on a standard medical checklist.

Pulmonary fibrosis does not only create questions about scans and pulmonary function tests. It can also create uncertainty around persistent cough, fatigue, exercise, work, sleep, travel, relationships, and how to explain changes that are difficult to put into words.

One question shared through the mama health app captured two concerns together:

“This dry cough just won't go away, and the fatigue is overwhelming.”

That experience cannot tell you why you feel a certain way or determine what a symptom means medically. It can help show the kinds of issues others with the same condition are trying to make sense of and give you ideas for topics you may want to raise at an appointment.

For more practical information, see mama health's guide to day-to-day life with fibrotic lung disease and its article on persistent dry cough and fatigue with pulmonary fibrosis.

How can mama health help before and between specialist appointments?

mama health is a free app for everything your condition asks of you, grounded in medical science and the experience of others, so you don't have to figure it out alone.

• Ask anything. Educational answers are shaped by trusted sources, your history, and thousands like you.
• Find specialists and care near you, wherever you are.
• You can also use mama health to get clearer educational explanations of your labs, prescriptions, and reports, read against the history you choose to share. This can make unfamiliar terminology easier to understand and help you decide which questions you want to bring to a healthcare professional.
• For your own reflection, you can record symptoms, medication experiences, appointments, triggers, and changes you want to remember. This information can then be organized into a structured report you can take to your doctor's appointment.

Seeing questions and experiences shared by thousands like you can provide another source of practical context. It may introduce an issue you had not thought to mention or help you find clearer words for something you have experienced yourself.

mama health does not diagnose pulmonary fibrosis, decide which specialist you need, determine which treatment is appropriate, or use your records to make clinical decisions.

Prepare for your next pulmonary fibrosis appointment

Keep your questions, reports, prescriptions, and the changes you want to remember together with mama health. You can find care nearby and create a structured report to take to your doctor's appointment.

What is the main takeaway when looking for pulmonary fibrosis care in Warsaw?

Warsaw has several strong specialist options, but they serve different needs within pulmonary fibrosis and ILD care.

PIM MSWiA now has a centre specifically dedicated to pulmonary fibrosis and combines ILD diagnostics with rheumatology and transplant expertise. The Institute of Tuberculosis and Lung Diseases has two departments with extensive ILD and pulmonary fibrosis experience and a broad specialist diagnostic infrastructure. WIM-PIB provides specialist pulmonology and an IPF programme. UCK WUM provides a more focused option when progressive fibrosing ILD is associated with systemic autoimmune disease.

Rather than choosing on reputation alone, compare the centre's expertise with the reason for your referral. Confirm current referral requirements and ask what medical records or imaging should be provided before the appointment.

Disclaimer: This content is informational and not a medical device. mama health offers information and support and does not replace a doctor.