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An infant case of hyperprolactinemia induced by a functional disorder of the hypothalamus
Toshihide Kubo1, Mahoko Furujo1
1Department of Pediatrics, National Hospital Organization, Okayama Medical Center, Okayama, Japan.
Insights
Functional hyperprolactinemia, a rare condition in children, was observed in a young boy. His gynecomastia and high prolactin levels resolved spontaneously within a year.
Area of Science:
- Pediatric Endocrinology
- Neuroendocrinology
Background:
- Functional hyperprolactinemia, typically originating in the hypothalamus, is infrequently reported in pediatric cases.
- Gynecomastia in young boys can be associated with elevated prolactin levels.
Purpose of the Study:
- To describe a case of functional hyperprolactinemia in a pediatric patient.
- To investigate the clinical presentation and diagnostic findings of hypothalamic-induced hyperprolactinemia in a child.
Main Methods:
- Case report of a 1-year-and-4-month-old boy presenting with gynecomastia.
- Hormonal assays including prolactin (PRL), gonadotropin-releasing hormone (GnRH), thyrotropin-releasing hormone (TRH), sex steroids, and adrenal androgens.
- Magnetic resonance imaging (MRI) of the brain and chromosomal analysis.
Main Results:
- The patient exhibited gynecomastia, elevated basal PRL levels (40.4 ng/ml), and prepubertal hormonal profiles.
- Normal PRL response to TRH and suppression of PRL by levodopa indicated a functional disorder.
- No organic brain lesions were detected by MRI, and chromosomal analysis was normal (46, XY).
- Gynecomastia and hyperprolactinemia resolved spontaneously within one year without intervention.
Conclusions:
- Functional hyperprolactinemia due to hypothalamic dysfunction can occur in young children.
- This condition may present with gynecomastia and typically resolves spontaneously.
- Non-invasive diagnostic methods and observation can be sufficient for managing pediatric functional hyperprolactinemia.
Abstract:
Although functional hyperprolactinemia originating in the hypothalamus has been observed, there have so far been few reports of this condition occurring in children. This report describes a 1-yr-and-4-mo old boy with hyperprolactinemia due to functional disorder of the hypothalamic region. He was referred to our hospital because of left gynecomastia which had been observed for one month. His left breast development was stage II, right breast stage I, and pubic hair stage I by Tanner stages, and his bilateral testicular volume was 1 ml. Both his height and growth velocity were normal and his bone age was not advanced. The basal PRL level was high (40.4 ng/ml), but other sex steroids and adrenal androgen levels were normal. GnRH demonstrated the prepubertal stage. PRL response to TRH was normal and levodopa suppressed the increased basal PRL level. His chromosomal finding was 46, XY and macroprolactinemia was ruled out. Repeated MRI examinations did not demonstrate any organic lesions in the brain. He was diagnosed as having hyperprolactinemia induced by a functional disorder of the hypothalamus. His gynecomastia reduced and the high PRL level decreased without medication after 1 year.
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