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Prolactin-secreting pituitary tumor in early adolescence: hormonal and electron microscopical studies.

Abstract
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.
AuthorsW G Schroffner
JournalArchives of internal medicine (Arch Intern Med) Vol. 136 Issue 10 Pg. 1164-8 (Oct 1976) ISSN: 0003-9926 [Print] United States
PMID971016 (Publication Type: Case Reports, Journal Article)
Chemical References
  • Prolactin
  • Growth Hormone
Topics
  • Adenoma, Chromophobe (blood, metabolism, ultrastructure)
  • Adolescent
  • Cytoplasmic Granules (ultrastructure)
  • Exocytosis
  • Glucose Tolerance Test
  • Growth Hormone (blood)
  • Humans
  • Male
  • Pituitary Gland (ultrastructure)
  • Pituitary Neoplasms (blood, metabolism, ultrastructure)
  • Prolactin (blood, metabolism)

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