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Pulmonary Fibrosis Journals | Open Access Journals
Pulmonary & Respiratory Medicine

Pulmonary & Respiratory Medicine

ISSN: 2161-105X

Open Access

Pulmonary Fibrosis Journals

Idiopathic pulmonary fibrosis (IPF) is the most common fibrosing lung disease and is associated with a very poor prognosis. IPF manifests histopathologically as usual interstitial pneumonia (UIP) and as subpleural and basal predominant reticulation with honeycombing on high-resolution computed tomography (HRCT) of the chest. When a high-confidence radiologic diagnosis of UIP is made on HRCT, surgical biopsy is rarely required.

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Citations: 1690

Pulmonary & Respiratory Medicine received 1690 citations as per Google Scholar report

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