A case of adrenocortical adenoma following long-term treatment in a patient with congenital adrenal hyperplasia / 소아과
Korean Journal of Pediatrics
; : 302-305, 2007.
Article
в En
| WPRIM
| ID: wpr-198442
Ответственная библиотека:
WPRO
ABSTRACT
As a result of the widespread use and enhanced quality of high-resolution radiological techniques, a recent report has revealed a relatively high prevalence of small adrenal tumors in patients with untreated congenital adrenal hyperplasia due to 21-hydroxylase deficiency. However, there are scarcely any pediatric cases of adrenocortical tumor following long-term treatment in patients suffering with congenital adrenal hyperplasia. We report here on a pediatric female case of adrenocortical adenoma despite adequate long-term treatment for the salt-losing type of congenital adrenal hyperplasia.
Key words
Полный текст:
1
База данных:
WPRIM
Основная тема:
Steroid 21-Hydroxylase
/
Prevalence
/
Adrenal Hyperplasia, Congenital
/
Adrenocortical Adenoma
Тип исследования:
Prevalence_studies
Пределы темы:
Female
/
Humans
Язык:
En
Журнал:
Korean Journal of Pediatrics
Год:
2007
Тип:
Article