Confrontation anatomo-clinique. Dyspnee progressive chez un homme de 58 ans

[en] Idiopathic pulmonary fibrosis and pulmonary fibrosis associated with systemic diseases are the most frequent diffuse interstitial pulmonary diseases. They slowly but irrevocably progress towards terminal respiratory failure. They can also be complicated by severe acute respiratory failure and admission in the intensive care unit can be discussed. Despite invasive mechanical ventilation, anti-infectious and immunosuppressive treatments, the disease carries a high mortality rate. We report and discuss the case of a patient with idiopathic, pulmonary fibrosis (UIP) who underwent rapid clinical deterioration.

Disciplines :

Cardiovascular & respiratory systems

Author, co-author :

Weber, T.

Broux, R.

Damas, François ; Université de Liège - ULiège > Services généraux (Faculté de médecine) > Relations académiques et scientifiques (Médecine)

de Leval, Laurence ; Université de Liège - ULiège > Département des sciences biomédicales et précliniques > Anatomie et cytologie pathologiques

Boniver, Jacques ; Université de Liège - ULiège > Département des sciences biomédicales et précliniques > Anatomie et cytologie pathologiques

Hermans, Gilberte ; Centre Hospitalier Universitaire de Liège - CHU > Anatomie pathologique

Language :

French

Title :

Confrontation anatomo-clinique. Dyspnee progressive chez un homme de 58 ans

Alternative titles :

[en] Anatomo-Clinical Confrontation: Idiopathic Pulmonary Fibrosis

Publication date :

2004

Journal title :

Revue Médicale de Liège

ISSN :

0370-629X

eISSN :

2566-1566

Publisher :

Université de Liège. Revue Médicale de Liège, Liège, Belgium

Volume :

Issue :

7-8, Jul-Aug

Pages :

430-4

Peer reviewed :

Peer reviewed

Available on ORBi :

since 19 December 2020

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Bibliography

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