Hypokalemic thyrotoxic periodic paralysis in a young Serbian male

  • Petar Ristić Military Medical Academy, Endocrinology Clinic, Belgrade, Serbia; University of Defence, Faculty of Medicine of the Military Medical Academy, Belgrade, Serbia
  • Tamara Dragović Military Medical Academy, Endocrinology Clinic, Belgrade, Serbia; University of Defence, Faculty of Medicine of the Military Medical Academy, Belgrade, Serbia
  • Saša Kiković Military Medical Academy, Endocrinology Clinic, Belgrade, Serbia;
  • Dragana Ristić Military Medical Academy, Ophtalmology Clinic, Belgrade, Serbia; University of Defence, Faculty of Medicine of the Military Medical Academy, Belgrade, Serbia
  • Marija Zdravković University Hospital Medical Center “Bežanijska Kosa”, Department of Cardiology, Belgrade, Serbia; University of Belgrade, Faculty of Medicine, Belgrade, Serbia
  • Saša Hinić University Hospital Medical Center “Bežanijska Kosa”, Department of Cardiology, Belgrade, Serbia
  • Tijana Durmić University of Belgrade, Faculty of Medicine, Institute of Forensic Medicine “Milovan Milovanović”, Belgrade, Serbia
  • Zoran Hajduković Military Medical Academy, Endocrinology Clinic, Belgrade, Serbia; University of Defence, Faculty of Medicine of the Military Medical Academy, Belgrade, Serbia
Keywords: hyperthyroidism;, hypokalemia;, paralysis, drug therapy;, treatment outcome

Abstract


Introduction. Hypokalemic thyrotoxic paralysis is a very rare form of periodic paralysis in Caucasian population. In this population, a more frequent form is familiar hypo­ka­lemic periodic paralysis with the same clinical presentation. It is flaccid paralysis of proximal muscles in extremities. Having in mind that clinical presentation of hyperthyro­idism in these patients is milder than it could be expected with given values of thyroid hormones, differential diagnosis to other forms of hypokalemic paralysis is essential. Case report. We presented a case of a young male with hyper­thyroidism and severe periodic flaccid paralysis particularly of leg muscles. Laboratory findings showed elevated thyroid hormones levels and hypokalemia during the attacks with normalized potassium levels between attacks. The patient had no relatives with the similar condition. Also, he never had anything like these attacks prior to development of hyperthyroidism. After differential diagnosis, other reasons for hypokalemic periodic paralysis were excluded. We inten­sified the hyperthyroidism treatment and resolved hypo­kalemic periodic paralysis attacks with potassium chloride (KCl) infusions. The patient was advised to start a definitive treatment of hyperthyroidism after stabilization of hormonal levels. Conclusion. Hypokalemic thyrotoxic para­lysis is a rare and potentially dangerous condition which, if reco­gnized, can be prevented by resolving hyperthyroxinemia and the use of nonselective β blockers.

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Published
2021/05/21
Section
Case report