CRANIOPHARYNGIOMA is frequently associated with dwarfism secondary to interference with hypothalamic or pituitary function or both. Persistence of pituitary insufficiency would be expected following removal of the tumor, whether or not hypophysectomy were a part of the surgical procedure. However, the maintenance or return of normal growth following surgery for craniopharyngioma has been suggested by several preliminary reports.1-4
We have observed a postoperative growth spurt followed by normal growth in a patient with preoperative growth retardation secondary to this lesion. The serum growth hormone response to hypoglycemia has been investigated preoperatively and postoperatively.
Report of a Case
The patient was admitted to the UCLA hospital at age 13 9/12 years (Oct 19, 1964) because of short stature, polyuria, polydipsia, and impaired vision.He had been noted to be short at age 7, but evaluation was not undertaken at that time. Beginning at age 8, the patient had the onset
Frasier SD, Smith FG. Return of Normal Growth Following Removal of a Craniopharyngioma. Am J Dis Child. 1968;116(3):311–314. doi:10.1001/archpedi.1968.02100020313014
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