Short Stature Without Neurological Manifestations in a Child with a Suprasellar Tumor

Abstract 

Addressing the problem of short stature in pediatrics is challenging because normal somatic growth depends on a complex interaction between genetic, nutritional, and hormonal factors. We report a 14-year-old girl with deceleration of growth velocity and delayed puberty but no other discernible neurologic or ophthalmologic symptoms or signs. Clonidine and insulin tolerance tests confirmed growth hormone deficiency, and magnetic resonance imaging disclosed a suprasellar mass. This case demonstrates that growth failure may be the only early sign of suprasellar tumor. Rigorous pursuit of the cause of a growth disorder should thus be considered, as it may disclose a potentially serious but treatable condition.

Keywords:  Growth hormone deficiency , Short stature , Suprasellar tumor

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