Residual pulmonary abnormalities in adult patients with chronic paracoccidioidiomycosis : prolonged observations after itraconazole therapy
ABSTRACT: Itraconazole effectively controls active paracoccidioidomycosis but appears not to hinder lung fibrosis. Clinical records and chest radiographs from 47 itraconazole-treated patients with prolonged posttherapy follow-up (mean follow-up period, 5.6 years) were analyzed; the radiographs were...
- Autores:
-
Tobón Orozco, Ángela María
Arango Arteaga, Myrtha
Restrepo Moreno, Ángela
Cano Restrepo, Luz Elena
Álvarez, Diego Luis
Osorio, Marta Lucía
Agudelo Restrepo, Carlos Andrés
- Tipo de recurso:
- Article of investigation
- Fecha de publicación:
- 2003
- Institución:
- Universidad de Antioquia
- Repositorio:
- Repositorio UdeA
- Idioma:
- eng
- OAI Identifier:
- oai:bibliotecadigital.udea.edu.co:10495/24086
- Acceso en línea:
- http://hdl.handle.net/10495/24086
- Palabra clave:
- Pulmón
Lung
Fibrosis Pulmonar
Pulmonary Fibrosis
Itraconazol
Itraconazole
Paracoccidioidomicosis
Paracoccidioidomycosis
Neumoconiosis
Pneumoconiosis
Radiografía Torácica
Radiography, Thoracic
- Rights
- openAccess
- License
- http://creativecommons.org/licenses/by-nc-nd/2.5/co/
| Summary: | ABSTRACT: Itraconazole effectively controls active paracoccidioidomycosis but appears not to hinder lung fibrosis. Clinical records and chest radiographs from 47 itraconazole-treated patients with prolonged posttherapy follow-up (mean follow-up period, 5.6 years) were analyzed; the radiographs were interpreted following pneumoconiosis standards that consider the lungs as 6 fields and grade damage according to the number of fields involved. Infiltrative lesions were observed at diagnosis in 93.6% of the patients. Fibrosis was observed in 31.8% of the patients at diagnosis and had not cleared at the end of the observation period in any of these patients. Fibrosis also developed de novo in 11 patients (25%), so that by the end of the follow-up period it was seen in 53.2% of patients overall. Fibrosis correlated with severity of infiltrates at diagnosis: fibrosis was present in 83% of patients with very severe infiltration and in 12.5% of patients with minor infiltration. Among patients with severe infiltration, fibrosis was present in 30%; this increased (to 75%) when bullae were concomitantly present at diagnosis. Prompt initiation of treatment is necessary to avoid the development of fibrosis. |
|---|
