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Updated: Aug 23, 2026

Endoscopic Endonasal Trans-sphenoidal Approach: Minimally Invasive Surgery for Pituitary Adenomas
Published on: January 17, 2018
Pituitary microadenomas in children: a cause of growth failure
Insights
Pituitary microadenomas in children can cause growth failure and growth hormone deficiency. Surgical removal of these tumors led to normal growth resumption in all studied patients.
Area of Science:
- Pediatric Endocrinology
- Neurosurgery
- Diagnostic Imaging
Background:
- Prepubertal idiopathic growth failure is a clinical challenge.
- Growth hormone deficiency can manifest as significant growth impairment.
- Pituitary microadenomas are rare causes of growth failure in children.
Purpose of the Study:
- To investigate the role of pituitary microadenomas in prepubertal growth failure.
- To evaluate diagnostic methods for identifying these microadenomas.
- To assess the efficacy of surgical intervention for tumor removal and growth restoration.
Main Methods:
- Case series of six children presenting with growth failure.
- Laboratory evaluation for growth hormone deficiency.
- Radiological assessment including skull X-rays, tomography, and CT scanning.
- Surgical tumor resection via a transsphenoidal approach.
Main Results:
- All six patients exhibited growth failure (≤2 cm/yr) and confirmed growth hormone deficiency.
- Standard radiography and tomography did not reveal significant sella turcica abnormalities.
- CT scanning successfully identified pituitary microadenomas as nodular areas of increased density.
- All patients experienced resumption of normal growth post-surgery.
Conclusions:
- Pituitary microadenomas should be considered in the differential diagnosis of prepubertal growth failure.
- CT scanning is crucial for diagnosing microadenomas not evident on conventional imaging.
- Transsphenoidal surgical resection is an effective treatment for restoring growth in affected children.
Abstract:
Six children, originally regarded as being affected by prepubertal idiopathic growth failure, were found to have pituitary microadenomas. In all six patients, the growth failure (less than or equal to 2 cm/yr) was the primary clinical sign, and was accompanied by a growth hormone deficiency that was discovered during the laboratory evaluation. Prominent alteration of the sella turcica was not demonstrated in the skull x-ray examinations of any of the children, even when the x-ray examinations were supplemented by hypocycloidal tomography. CT scanning proved to be a very useful integrating diagnostic procedure, revealing the adenoma to be a nodular area of increased density within the sella turcica. In all of the children, resumption of normal growth was obtained following the surgical removal of the tumor through a transsphenoidal approach.
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