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Diagnosis and management of precocious puberty in atypical presentations of McCune-Albright syndrome: a case series review.
Bercaw-Pratt, Jennifer L; Moorjani, Tracy Patel; Santos, Xiomara M; Karaviti, Lefkothea; Dietrich, Jennifer E.
Afiliación
  • Bercaw-Pratt JL; Division of Pediatric and Adolescent Gynecology, Baylor College of Medicine, Houston, Texas, USA. jbercaw@bcm.edu
J Pediatr Adolesc Gynecol ; 25(1): e9-e13, 2012 Feb.
Article en En | MEDLINE | ID: mdl-22051789
BACKGROUND: McCune-Albright syndrome is a rare syndrome, classically defined as the triad of precocious puberty, fibrous dysplasia of bone, and café au lait lesions. Partial or atypical presentations of McCune-Albright syndrome, with only one or two of the classic symptoms, have been described in the literature and remain particularly challenging due to lack of diagnostic phenotype. In these patients, the utility of analysis of mutations in the gene of the α subunit of the stimulatory G-protein is limited and so the diagnosis is often based on clinical judgment. Three atypical cases of suspected McCune-Albright syndrome with gonadotropin-independent precocious puberty are presented. CASES: Case #1: A 5-year-old female presented with painlesss vaginal bleeding and was found to have café au lait lesions. She was diagnosed with gonadotropin independent precocious puberty with eventual progression to gonadotropin dependent precocious puberty which was successfully treated with both letrozole and gonadotropin-releasing hormone agonist therapy. Case #2: A 3-year-old female presented with painless vaginal bleeding and was found to have café au lait lesions. She was diagnosed with gonadotropin independent precocious puberty and was successfully treated with letrozole. Case #3: A 5-year-old female presented with fibrous dysplasia and was found to have evidence of uterine and ovarian enlargement on ultrasound. She was diagnosed with gonadotropin-independent precocious puberty and was successfully treated with letrozole. SUMMARY AND CONCLUSION: Although different in presentation, all three atypical cases of suspected McCune-Albright syndrome with gonadotropin-independent precocious puberty were successfully treated with aromatase inhibitors. This small case series shows the utility and efficacy of aromatase inhibitors in the setting of atypical cases of suspected MAS with gonadotropin-independent precocious puberty.
Asunto(s)

Texto completo: 1 Colección: 01-internacional Asunto principal: Pubertad Precoz / Triazoles / Inhibidores de la Aromatasa / Displasia Fibrosa Poliostótica / Nitrilos Tipo de estudio: Diagnostic_studies / Literature_review Límite: Child, preschool / Female / Humans Idioma: En Revista: J pediatr adolesc gynecol Asunto de la revista: GINECOLOGIA / PEDIATRIA Año: 2012 Tipo del documento: Article País de afiliación: Estados Unidos

Texto completo: 1 Colección: 01-internacional Asunto principal: Pubertad Precoz / Triazoles / Inhibidores de la Aromatasa / Displasia Fibrosa Poliostótica / Nitrilos Tipo de estudio: Diagnostic_studies / Literature_review Límite: Child, preschool / Female / Humans Idioma: En Revista: J pediatr adolesc gynecol Asunto de la revista: GINECOLOGIA / PEDIATRIA Año: 2012 Tipo del documento: Article País de afiliación: Estados Unidos