A thyrotropin-secreting pituitary adenoma as a cause of thyrotoxic periodic paralysis

AMW Alings, E Fliers*, WW de Herder, LJ Hofland, HE Sluiter, TP Links, JH van der Hoeven, WM Wiersinga

*Corresponding author for this work

Research output: Contribution to journalArticleAcademicpeer-review

24 Citations (Scopus)

Abstract

We describe a patient with thyrotoxic periodic paralysis (TPP) caused by a thyrotropin-secreting pituitary adenoma. The diagnosis TPP was based on the combination of episodes of reversible hypokalaemic paralysis, hyperthyroidism and electrophysiological findings. A thyrotropin-secreting pituitary adenoma was diagnosed on the basis of endocrinological function tests and MRI of the pituitary gland. Before transsphenoidal resection of the adenoma, treatment with octreotide restored euthyroidism both clinically and biochemically. Immunocytochemistry of the pituitary adenoma was positive for TSH exclusively. Incubation with octreotide or quinagolide induced decreased TSH and alpha-subunit production by the cultured adenoma cells, in agreement with the preoperative in vivo data. This paper is the first to describe in vivo and in vitro characteristics of a thyrotropin-secreting pituitary adenoma in a patient presenting with periodic paralysis. (J. Endocrinol. Invest. 21: 703-706, 1998) (C)1998, Editrice Kurtis.

Original languageEnglish
Pages (from-to)703-706
Number of pages4
JournalJournal of endocrinological investigation
Volume21
Issue number10
Publication statusPublished - Nov-1998

Keywords

  • hypokalemia
  • thyrotoxicosis
  • TSH
  • pituitary tumor
  • hyperthyroidism
  • OCTREOTIDE

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