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Idiopathic pulmonary fiborsis (IPF) is mostly diagnosed in advanced stage

E Mušiè, L Debevec, P Kecelj, R Eržen, R Cesar · Pneumologie · 2004 · Heft 03

Dokument
1161765
CareLit-ID
Jahr
2004
Publikation
PDF
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Metadaten
DOI
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Bibliografische Angaben

Zeitschrift
Pneumologie
Autor:innen
E Mušiè, L Debevec, P Kecelj, R Eržen, R Cesar
Ausgabe
Heft 03 / 2004
Seiten
–
Erschienen: 2004-03-10 00:00:00
ISSN
0934-8387

Zusammenfassung

Background: IPF is lung disease of unfavorable prognosis. Earliest stages are responsive to treatment. Late diagnosis causes bad outcome. Patients and methods: 32 cases of IPF were diagnosed in 2 years. Mean age was 64 years. Symptoms, chest radiograph, lung function were assessed in all, HRCT, lung bioppsy in 18 and BAL in 22 cases. In advanced stage of 20 cases no therapy has been introduced. Results: Leading symptom was dyspnoe in 20 patients, cough in 8 others. X-ray showed reticular pattern, predilectionnaly peripheroposterobasal in 27 cases, ground glass only in 5. Reduction of lung volume was in 24 cases.…

Schlagworte

Diagnosis Biopsy Diffusion Pneumologie