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Published on: January 17, 2018
Hyperprolactinemia in children: clinical features and long-term results
Gonul Catli1, Ayhan Abaci, Ayca Altincik
1Department of Pediatric Endocrinology, School of Medicine, Dokuz Eylul University, 35340 Balcova, Izmir, Turkey.
Childhood hyperprolactinemia, often caused by pituitary adenomas, presents with menstrual issues, headaches, and galactorrhea. Medical treatment is typically first-line, with surgery reserved for specific cases.
Area of Science:
- Pediatric Endocrinology
- Neuroendocrinology
- Oncology
Background:
- Hyperprolactinemia is a rare endocrine disorder in children.
- It can be caused by pituitary adenomas (microadenoma or macroadenoma) or be idiopathic.
- Understanding its etiology and clinical presentation is crucial for management.
Purpose of the Study:
- To retrospectively review the etiologic reasons for hyperprolactinemia in pediatric patients.
- To analyze the clinical features and treatment outcomes of childhood hyperprolactinemia.
Main Methods:
- Retrospective chart review of 11 female patients diagnosed with hyperprolactinemia.
- Analysis of patient demographics, adenoma characteristics, presenting symptoms, and treatment modalities.
- Evaluation of treatment responses and surgical indications.
Main Results:
- The mean age at diagnosis was 14.2 years.
- Common symptoms included menstrual disorders, headache, and galactorrhea; obesity was noted in one-third.
- Bromocriptine was the primary treatment; cabergoline was used in a few cases.
- One patient with macroadenoma underwent surgery due to cavernous sinus invasion and visual field defect.
Conclusions:
- Medical management (bromocriptine, cabergoline) is the recommended first-line treatment for pediatric hyperprolactinemia, including both microadenoma and macroadenoma.
- Surgical intervention is indicated only for specific cases with neurological compromise or invasive disease.
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