Abstract
Idiopathic pulmonary fibrosis (IPF) has a poor prognosis and therapeutic options are limited with a 5-year survival of less than 50%. This report includes a case of histologically confirmed IPF in a patient whose native lung showed objective improvement as measured by high-resolution CT while he was receiving cyclosporine-based immunosuppressive therapy after single-lung transplantation.
Original language | English |
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Pages (from-to) | 1478-1481 |
Number of pages | 3 |
Journal | Chest |
Volume | 114 |
Issue number | 5 |
Publication status | Published - 1998 |
Keywords
- Cyclosporine
- Idiopathic pulmonary fibrosis
- Lung transplantation