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  Vol. 136 No. 10, October 1976 TABLE OF CONTENTS
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Prolactin-Secreting Pituitary Tumor in Early Adolescence

Hormonal and Electron Microscopical Studies

Werner G. Schroffner, MD

Arch Intern Med. 1976;136(10):1164-1168.


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 an 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.

(Arch Intern Med 136:1164-1168, 1976)



Author Affiliations

From the Department of Medicine, University of Hawaii School of Medicine and the Fronk Clinic, Honolulu.


Footnotes

Received for publication Sept 20, 1975; accepted March 8, 1976.

Read in part before the Hawaii Regional Meeting, American College of Physicians, Honolulu, April 12, 1975.

Reprint requests to the Fronk Clinic, 839 S Beretania St, Honolulu, HI 96813 (Dr Schroffner).



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THIS ARTICLE HAS BEEN CITED BY OTHER ARTICLES

Prolactin-Secreting Macroadenomas in Adolescents: Response to Bromocriptine Therapy
Tyson et al.
Arch Pediatr Adolesc Med 1993;147:1057-1061.
ABSTRACT  

Long-term Bromocriptine Treatment for Prolactin-Secreting Macroadenoma
HUSEMAN et al.
Arch Pediatr Adolesc Med 1986;140:1216-1217.
ABSTRACT  





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