Case report details effective treatment for multiple endocrinopathies in a child with McCune-Albright syndrome, suggesting long-term strategies for care.
Key Points
The patient's complex presentation included hyperfunctioning endocrinopathies and fibrous dysplasia, necessitating tailored treatment.
At 8 years old, the girl exhibited multiple endocrinopathies originating from GNAS gene mutations, such as growth hormone excess.
Management involved carbimazole, letrozole, lanreotide, and zoledronic acid to address complex hormonal interactions.
This report underscores the need for comprehensive long-term follow-up in pediatric cases of McCune-Albright syndrome.