[Precocious puberty caused by McCune-Albright syndrome in a girl aged 6 years and 9 months]. / Przedwczesne dojrzewanie plciowe w zespole McCune-Albrighta u dziewczynki w wieku 6 lat i 9 miesiecy.
Endokrynol Diabetol Chor Przemiany Materii Wieku Rozw
; 12(1): 63-7, 2006.
Article
em Pl
| MEDLINE
| ID: mdl-16704864
ABSTRACT
The McCune-Albright syndrome is characterised by polyostotic fibrous dysplasia, "cafe-au-lait" spots and autonomous hyperfunction of various endocrine organs. The authors present the case of a girl at the age of 6 years 9 months with precocious puberty (thelarche III, menarche). High estradiol level (204 pg/ml) and low gonadoptopins concentration as well as their level after GnRH administration suggested ovarian autonomy. Ovarian cysts were found on pelvic ultrasound. Other endocrine abnormalities were excluded. Single "cafe-au-lait" spot was found on the patient skin. Scintigraphy, radiography and computed tomography scans showed fibrous dysplastic bones in the right tibia and in maxillary and sphenoid sinuses.
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Coleções:
01-internacional
Base de dados:
MEDLINE
Assunto principal:
Puberdade Precoce
/
Displasia Fibrosa Poliostótica
Tipo de estudo:
Diagnostic_studies
/
Etiology_studies
Limite:
Child
/
Female
/
Humans
Idioma:
Pl
Ano de publicação:
2006
Tipo de documento:
Article