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1.
Article de Coréen | WPRIM | ID: wpr-20663

RÉSUMÉ

PURPOSE: The purpose of this study was to evaluate the efficacy and metabolism of inhaled steroids to prevent recurrent wheezing after bronchiolitis. METHODS: Sixty two patients were randomly divided into study (n=31) and control (n=31) groups. All of them received budesonide 500 microgram and salbutamol 1.25 mg 4 times a day via nebulizer during admission period (5.5+/-2.5 days). After discharge, the study group patients received fluticasone 50 microgram twice a day with metered dose inhaler with mask spacer for 12 weeks, and the control group received none of inhaled steroids. Serum cortisol and dehydroepiandrosterone sulfate (DHEA-S) concentrations were measured at admission and at the end of the inhaled corticosteroid (ICS) therapy. Weight and height of all patients were checked during the follow-up period. RESULTS: Atopic dermatitis of the patient and allergy family history proved statistically significant. Among high risk group patients, the attack rate of recurrent wheezing in the study group was significantly reduced as compared with the control group. Cortisol levels checked at the end of the ICS therapy were not significantly different from the level checked at admission. In the study group, there was no statistically significant difference between dehydroepiandrosterone sulfate (DHEA-S) level at admission and at the end of the ICS therapy. There was no statistically significant difference of height and weight SDS (standard deviation score) between baseline and 12 weeks later. CONCLUSION: This study suggest that inhaled corticosteroid can be used prophylactically for reducing recurrent wheezing after bronchiolitis in high risk group for asthma.


Sujet(s)
Humains , Salbutamol , Asthme , Bronchiolite , Budésonide , Sulfate de déhydroépiandrostérone , Eczéma atopique , Études de suivi , Hydrocortisone , Hypersensibilité , Masques , Métabolisme , Aérosols-doseurs , Nébuliseurs et vaporisateurs , Bruits respiratoires , Stéroïdes , Fluticasone
2.
Article de Coréen | WPRIM | ID: wpr-59288

RÉSUMÉ

Hepatoblastoma is a rare pediatric malignancy which frequently presents at an advanced unresectable stage. Complete surgical resection after chemotherapy is the definitive treatment for hepatoblastoma. Liver transplantation should be considered for children who have unresectable hepatoblastoma. We report a case of a 18-month-old boy with unresectable hepatoblastoma who had transplantation with pre- and post-operative chemotherapy.


Sujet(s)
Enfant , Humains , Nourrisson , Mâle , Traitement médicamenteux , Hépatoblastome , Transplantation hépatique , Foie , Donneur vivant
3.
Article de Coréen | WPRIM | ID: wpr-70087

RÉSUMÉ

PURPOSE: To demonstrate the bystander effect in murine neuroblastoma model which transduced with HSV-TK gene in vitro and in vivo. METHODS: The LNC/TK vector was transfered in vitro into the neuro-2a cells, murine neuroblastoma cell line. Variable mixed populations of neuro-2a cells consisting of HSV-TK+ or HSV-TK- were plated into culture plates and treated with GCV for another 4 days. Surviving cells were counted and cell viability was determinated. For investigating the in vivo bystander effect, variable mixed populations of neuro-2a cells consisting of HSV-TK+ and HSV-TK- were inoculated into A/J mice. The tumor size was measured following injection of GCV for 7 days. RESULTS: The survival rate of the 100% neuro-2a/TK group was 90%, 25%, 5% and 0%, of 50% neuro-2a/TK group was 92%, 30%, 10% and 0%, and of the 10% neuro-2a/TK group was 95%, 40%, 15% and 5%. But, the survival rate of 0% neuro-2a/TK group was 120%, 150%, 180% and 220% on days 1, 2, 3, and 4 respectively. In the 100% and 50% neuro-2a/TK groups, tumor had disappeared following administration of GCV and in 10% neuro-2a/TK group, tumor size was not increased during GCV treatment. In 0% neuro-2a/TK group, tumor size increased during administration of GCV and all mice died after 6 weeks. CONCLUSIONS: We demonstrated the bystander effect in a murine neuroblastoma model which transduced with HSV-TK gene in vitro and in vivo. These results suggest that HSV-TK/GCV gene therapy may be useful for treatment of neuroblastoma.


Sujet(s)
Animaux , Souris , Effet bystander , Lignée cellulaire , Survie cellulaire , Thérapie génétique , Neuroblastome , Taux de survie
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