Your browser doesn't support javascript.
loading
Montrer: 20 | 50 | 100
Résultats 1 - 1 de 1
Filtrer
Plus de filtres








Gamme d'année
1.
Article de Coréen | WPRIM | ID: wpr-89109

RÉSUMÉ

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.


Sujet(s)
Enfant , Humains , Adénome oxyphile , Glandes surrénales , Syndrome de Cushing , Sulfate de déhydroépiandrostérone , Féminisation , Hyperaldostéronisme , Enfant d'âge préscolaire , Puberté précoce , Testostérone , Virilisme
SÉLECTION CITATIONS
DÉTAIL DE RECHERCHE