A 13-year-old boy was evaluated for an enlarged sella. There were no consistent visual field defects, and carotid arteriograms and pneumoencephalograms showed no extrasellar abnormality. The endocrine workup demonstrated a subnormal
growth hormone reserve. The only other, but most striking abnormality, was an excessively high serum
prolactin level, which was partially suppressed with
levodopa. A chromophobe
pituitary tumor was removed that had histological features suggestive of
malignant neoplasm. Characteristics of a
prolactin-secreting
tumor were confirmed by electron microscopy. The serum
prolactin levels decreased substantially after surgery and further after a course of
pituitary irradiation; however, they continue to be elevated above normal.
Prolactin determinations play in integral part in the evaluation for a possible
pituitary tumor-not only for diagnostic purposes, but also to provide a parameter of future
tumor activity in an established case. Electron microscopical studies are helpful in identifying the
tumor as source of the excessive
prolactin secretion.