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Hypothalamic-pituitary dysfunction in survivors of childhood brain tumors in Prasat Neurological Institute
Apasri Lusawat1, Kanlaya Dhiravibulya, Sasipa Thammongkol
1Department ofPediatric Neurology, Prasat Neurological Institute, Bangkok, Thailand. lusawat@hotmail.com
Insights
Childhood brain tumor survivors frequently experience hypothalamic-pituitary dysfunction, impacting growth hormone and adrenal function. Regular monitoring is crucial for managing these endocrine issues and improving survivors' quality of life.
Area of Science:
- Pediatric Endocrinology
- Neuro-oncology
- Clinical Research
Background:
- Childhood brain tumors pose significant long-term health challenges.
- Survivors often develop endocrine complications due to treatment and tumor location.
- Hypothalamic-pituitary dysfunction is a common sequela requiring careful assessment.
Purpose of the Study:
- To evaluate the prevalence and types of hypothalamic-pituitary dysfunction in childhood brain tumor survivors.
- To compare dysfunction between tumors directly and indirectly affecting the hypothalamic-pituitary axis.
- To inform clinical monitoring and management strategies for these survivors.
Main Methods:
- A cohort of 19 childhood brain tumor survivors, at least 2 years post-treatment without recurrence, was studied.
- Patients were classified as directly (DHPA) or indirectly (IDHPA) involving the hypothalamic-pituitary axis.
- Hormonal assessments included Growth Hormone (GH) stimulation tests, ACTH stimulation tests, and thyroid function tests (TFTs).
Main Results:
- 73% of survivors exhibited Growth Hormone Deficiency (GHD).
- High rates of adrenal insufficiency (85% DHPA, 10% IDHPA) and central hypothyroidism (100% DHPA, 10% IDHPA) were observed.
- Tumor location directly impacting the axis (DHPA) correlated with more severe dysfunction.
Conclusions:
- Childhood brain tumor survivors, particularly those with DHPA, are at high risk for significant hypothalamic-pituitary dysfunction.
- Regular endocrine monitoring is essential for early detection and management.
- Proactive management can mitigate morbidity and enhance the quality of life for survivors.
Objective:
To assess hypothalamic-pituitary dysfunction in childhood brain tumor survivors in Prasat Neurological Institute.
Material And Method:
Between October 2007 and September 2008, 19 brain tumor survivor children in Prasat Neurological Institute without recurrence at least 2 years after complete treatment were included in the present study. The patients were categorized according to brain tumor location into directly (DHPA) (9 cases) and indirectly (IDHPA) (10 cases) involving hypothalamic-pituitary axis. All patients were treated by surgery. Furthermore, six cases were combined with radiation and chemotherapy and 10 cases were combined with radiation therapy only. Growth Hormone (GH) stimulation test by clonidine and/or L-Dopa, ACTH stimulation test and thyroid function test (TFT) were done.
Results:
The mean age at diagnosis was 9.9 +/- 4.6 years old and the interval from diagnosis to study was 5.8 +/- 2.2 years. Seven DHPA (77%) and seven IDHPA patients (70%) had low peak GH with significant lower level in the former group (p < 0.05). Six of seven DHPA (85%) and one IDHPA patients (10%) had low response to ACTH stimulation test. All DHPA (100%) and 10% IDHPA patients had central hypothyroidism. By ACTH stimulation test in DHPA patients, hypocortisolism was detected in five and excluded in one who later stopped prednisolone after prolonged continuation. The central hypothyroidism was newly detected in two DHPA patients and replacement therapy was initiated GH deficiency (GHD) was detected by GH stimulation test in 73% of overall brain tumors. Growth hormone therapy would be considered in the appropriate GHD patients.
Conclusion:
With effective therapy and improving survival rates of brain tumor children, hypothalamic-pituitary dysfunction in either DHPA or IDHPA group should be regularly monitored to prevent further morbidity and improve quality of life.
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