Idiopathic Diffuse Interstitial Pulmonary Fibrosis

Idiopathic diffuse interstitial pulmonary fibrosis is a disease in which the tissue between the alveoli of the lungs becomes scarred and stiff progressively, without a clearly identifiable cause.

Manifestations that are described: Shortness of breath that increases with exertion, persistent dry cough, and tiredness are usually noticed.

When to see a doctor? If you have difficulty breathing that worsens over time or a dry cough that does not resolve, a detailed evaluation is advisable.

Which specialist treats it? The pulmonologist is the professional who studies diseases of the lung, including those that affect the interstitial tissue, and follows their evolution. Seeing a doctor at the first respiratory symptoms helps to understand the source of the discomfort and plan care.