EAP 2019 Congress and MasterCourse

Precocious Puberty: When the Cause is not Idiopathic

Ana Luísa Leite 1 Elisa Galo 3 Ana Antunes 6 Brígida Robalo 4 Filipa Espada 7 Sofia Castro 2 Catarina Limbert 5
1Unidade de Endocrinologia e Diabetologia Pediátrica, Centro Hospitalar de Vila Nova de Gaia / Espinho, Portugal
2Serviço de Pediatria, Centro Hospitalar Barreiro Montijo, Portugal
3Serviço de Pediatria, Hospital da Luz, Portugal
4Unidade de Endocrinologia Pediátrica, Centro Hospitalar Universitário Lisboa Norte, Portugal
5Unidade de Endocrinologia Pediátrica, Centro Hospitalar Universitário de Lisboa Central, Portugal
6Unidade de Endocrinologia Pediátrica, Hospital de Braga, Portugal
7Unidade de Endocrinologia Pediátrica, Hospital Pedro Hispano, Portugal

Precocious Puberty is defined by the onset of pubertal development at an age 2-2,5 standard deviations earlier than the normal population, which means before nine years old in boys and eight years in girls. Central Precocious Puberty (CPP) is diagnosed when the hypothalamic-pituitary axis is activated. Although the majority of CPP causes are idiopathic, secondary causes should be discharged because of pathologic conditions with significant risk of morbidity and even death.

Aims: To evaluate the prevalence of secondary CPP in the Portuguese population in the last five years, to characterize anthropometric and imagological features and identify its clinical predictors.

Methods: Cross-sectional study from a National Digital Database, enrolled from eleven Public and Private Pediatric Endocrine Departments. Cases reported from January 2013 to December 2017. Statistical analysis was performed using SPSSTM 23.0 version.

Results: A total of 210 cases presented CPP during the last five years. 187 (89%) were female. The median age of diagnosis was 6,5 years old in idiopathic CPP and 4,8 years old in secondary CPP (p=0,002). Only 146 (69.5%) enrolled hypophyses/cranial image and secondary cases of CPP were identified in 38 patients (26%). Tumors were diagnosed in ten cases (26,3% of the secondary CPP) and the most frequent was hamartoma in 60%. From the secondary cases of CPP only 17 were male (12%) and there were no significant differences among gender when considering idiopathic/secondary cases. There was a negative correlation between the age of clinical manifestations (p<0.001) and secondary CPP.

Conclusions: CPP is more frequent in girls, either in idiopathic or secondary cases. The yearly age of clinical manifestations is a better predictor than gender in the diagnosis of secondary CPP.









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