A Case of adrenocortical oncocytoma Presenting with Peripheral Precocious Puberty
Annals of Pediatric Endocrinology & Metabolism
;
: 49-52, 2012.
Article
Dans Coréen
| WPRIM
| ID: wpr-89109
ABSTRACT
Adrenocortical oncocytoma is a rare adrenal gland tumor, and in most cases, benign and non-functioning. Functional adrenocortical oncocytoma has only been reported in eleven cases worldwide, including three children. These cases all showed clinical symptoms and signs, such as virilization, feminization, Cushing syndrome and Conn syndrome, as a result of overproduction of adrenal steroid hormones. We report a 2-year-old girl who presented with precocious puberty with premature pubarche. Dehydroepiandrosterone sulfate (DHEA-S) and testosterone levels were elevated and a 1.9 cm right adrenocortical oncocytoma was found. After tumor resection, her hormone levels were normalized.
Texte intégral:
Disponible
Indice:
WPRIM (Pacifique occidental)
Sujet Principal:
Puberté précoce
/
Testostérone
/
Virilisme
/
Enfant d'âge préscolaire
/
Glandes surrénales
/
Adénome oxyphile
/
Sulfate de déhydroépiandrostérone
/
Syndrome de Cushing
/
Féminisation
/
Hyperaldostéronisme
Limites du sujet:
Enfant
/
Humains
langue:
Coréen
Texte intégral:
Annals of Pediatric Endocrinology & Metabolism
Année:
2012
Type:
Article
Documents relatifs à ce sujet
MEDLINE
...
LILACS
LIS