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Published on: November 14, 2013
Pituitary imaging findings in pediatric patients with idiopathic hypogonadotropic hypogonadism
Eda Celebi Bitkin1, Nursen Toprak2, Serap Karaman3
1Division of Pediatric Endocrinology, Department of Pediatrics, Faculty of Medicine, Van Yuzuncu Yil University, Van, Turkey.
Insights
Idiopathic hypogonadotropic hypogonadism in children is linked to hypothalamic-pituitary abnormalities. Pituitary imaging is crucial for diagnosing these conditions in pediatric patients.
Area of Science:
- Pediatric Endocrinology
- Neuroendocrinology
- Radiology
Background:
- Idiopathic hypogonadotropic hypogonadism (IHH) in children results in absent puberty.
- Hypogonadotropic hypogonadism stems from hypothalamic or pituitary defects.
- Pituitary magnetic resonance imaging (MRI) is standard for IHH evaluation.
Purpose of the Study:
- To investigate pituitary pathologies in children with IHH.
- To correlate pituitary MRI findings with IHH in a pediatric cohort.
Main Methods:
- Retrospective analysis of 22 pediatric patients with IHH.
- Recorded age, gender, history, physical exam, and lab tests.
- Examined pituitary MRI results for abnormalities.
Main Results:
- 22 pediatric patients diagnosed with hypogonadotropic hypogonadism.
- Low luteinizing hormone and follicle-stimulating hormone levels observed.
- Pituitary MRI revealed adenoma (6), empty sella (1), and hypoplasia (5).
Conclusions:
- Hypothalamic-pituitary abnormalities are more prevalent in pediatric IHH than in adults.
- Emphasizes the critical role of pituitary imaging in diagnosing pediatric IHH.
- Early detection of pituitary pathologies aids in managing IHH.
Abstract:
Objective. Idiopathic hypogonadotropic hypogonadism in children is a disease leading to a puberty absence. Some hypothalamic and pituitary defects cause hypogonadotropic hypogonadism. Pituitary magnetic resonance imaging is routinely performed in these patients. In our study, we provide an information about pituitary pathologies associated with an idiopathic hypogonado-tropic hypogonadism in childhood. Methods. Twenty-two patients, who were admitted to the pediatric endocrine outpatient clinic of our hospital because of their undeveloped secondary sex characteristics during adolescence, were included in our study. Age, gender, history, physical examination findings, and laboratory tests were recorded in patients. Pituitary magnetic resonance imaging results were examined. The criteria for the diagnosis of hypogonadism were: absence of puberty or delayed puberty, clinical signs or symptoms of hypogonadism, and presence of low or normal gonadotropin levels. Results. In the present study, 22 patients were diagnosed with hypogonadotropic hypogonadism. The mean age of the patients was 15.90±1.09 years. Basal and stimulated luteinizing hormone and follicular stimulating hormone levels of the patients were found to be low. Prolactin, cortisol, adrenocorticotropic hormone, free thyroxine, and thyroid stimulating hormone levels were within normal limits in all patients. The pituitary magnetic resonance imaging revealed six patients with pituitary adenoma, one with empty sella turcica, and five with pituitary hypoplasia. Conclusions. The present data showed that in the presence of hypogonadotropic hypogonadism, the hypothalamic-pituitary abnormalities are more likely to be present in the children compared to the adult population. Thus, it can be strongly emphasized the importance of the pituitary imaging examination, especially in the idiopathic hypogonadotropic hypogonadism cases.
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