The First Successful Lung Transplantation in a Korean Child with Cystic Fibrosis
Journal of Korean Medical Science
; : 2073-2078, 2017.
Article
en En
| WPRIM
| ID: wpr-158106
Biblioteca responsable:
WPRO
ABSTRACT
Cystic fibrosis (CF) is an autosomal recessive inherited multisystem disorder caused by mutations of the gene encoding the cystic fibrosis transmembrane conductance regulator (CFTR) protein. Respiratory failure remains the most frequent cause of morbidity and mortality. Lung transplantation is the only option to treat end-stage lung disease. Very few cases of CF occur in Koreans. We report the case of a 12-year-old girl with respiratory failure due to CF who underwent lung transplantation. She had been diagnosed with CF 8 years previously after being treated for recurrent Pseudomonas aeruginosa pneumonia and malnutrition based on sweat chloride concentrations and the CFTR protein gene mutation test. Progression to end-stage lung disease and respiratory failure led to registration with the Korean Network for Organ Sharing. She underwent successful double lung transplantation in 2014. Although she has diabetes mellitus and chronic kidney disease, she has a better quality of life and a prolonged life expectancy.
Palabras clave
Texto completo:
1
Banco de datos:
WPRIM
Asunto principal:
Neumonía
/
Pseudomonas aeruginosa
/
Calidad de Vida
/
Insuficiencia Respiratoria
/
Sudor
/
Esperanza de Vida
/
Mortalidad
/
Trasplante de Pulmón
/
Regulador de Conductancia de Transmembrana de Fibrosis Quística
/
Fibrosis Quística
Tipo de estudio:
Prognostic_studies
Límite:
Child
/
Female
/
Humans
País/Región como asunto:
Asia
Idioma:
En
Revista:
Journal of Korean Medical Science
Año:
2017
Tipo del documento:
Article