A Boy with Adrenocortical Tumor Who Progressed to Central Precocious Puberty after Surgery
Annals of Pediatric Endocrinology & Metabolism
;
: 57-61, 2012.
Artículo
en Coreano
| WPRIM
| ID: wpr-89107
ABSTRACT
Adrenocortical tumors in children are rare and show various clinical symptoms. We present an 8-year-old boy with peripheral precocious puberty caused by adrenocortical tumor. He showed elevated serum DHEA-S and 17-hydroxyprogesterone, and computed tomography revealed an abdominal mass. After surgical resection, he developed central precocious puberty. We report a rare case that showed progression from peripheral precocious puberty to central precocious puberty.
Texto completo:
Disponible
Índice:
WPRIM (Pacífico Occidental)
Asunto principal:
Pubertad Precoz
/
Neoplasias de la Corteza Suprarrenal
/
17-alfa-Hidroxiprogesterona
Límite:
Niño
/
Humanos
Idioma:
Coreano
Revista:
Annals of Pediatric Endocrinology & Metabolism
Año:
2012
Tipo del documento:
Artículo
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