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Pediatric Pituitary Adenomas and Cysts: A 46-Year Population-Based Analysis
Kaitlin Leopold1, Mostafa Salama1, Seema Kumar1
1Division of Pediatric Endocrinology and Metabolism, Department of Pediatric and Adolescent Medicine, Mayo Clinic, Rochester, MN 55905, USA.
Journal of the Endocrine Society
|May 5, 2025
Summary
Pediatric pituitary adenomas and cysts are rare, with most being small and nonfunctioning. These lesions are typically stable over time, requiring further study for long-term management strategies.
Area of Science:
- Pediatric Endocrinology
- Neuro-oncology
- Epidemiology
Background:
- Pituitary adenomas and cysts are uncommon in children, necessitating a better understanding for effective management.
- Improved knowledge of pediatric pituitary lesions can inform clinical practice guidelines.
Purpose of the Study:
- To determine the incidence, clinical presentation, management, and outcomes of pituitary adenomas and cysts in a pediatric population.
- To investigate correlations between lesion characteristics (size, headaches) and disease progression, and MRI rates.
Main Methods:
- Retrospective cohort study of pediatric patients (≤18 years) with pituitary adenomas/cysts in Olmsted County, MN (1976-2021).
- Utilized Rochester Epidemiology Project diagnostic codes to identify 37 confirmed cases from 234 unique patients.
- Calculated incidence rates and analyzed clinical data using descriptive statistics.
Main Results:
- Incidence was 2.29 cases per 100,000 person-years.
- Most common types were nonfunctioning (68%) and prolactinomas (27%); GH- and TSH-secreting adenomas were rare.
- Median lesion size was 5.5 mm; median follow-up was 7.4 years. Disease progression occurred in 4 patients, stabilizing with treatment. No significant correlation found between MRI rates, lesion size, or headaches and disease progression.
Conclusions:
- Pediatric pituitary adenomas and cysts are rare, often small, nonfunctioning, and demonstrate stability during long-term follow-up.
- Further large-scale studies are required to elucidate the natural history of small, nonfunctioning pituitary lesions and refine management recommendations.
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