Key result
Thyrotoxic periodic paralysis in a 28-year-old male presented with severe hypokalemia (2.0 mmol/L) and ventricular tachycardia, which was successfully managed with antithyroid therapy.
Case Report (n=1)
No
Thyrotoxic periodic paralysis can present with life-threatening ventricular arrhythmias and cardiac arrest, highlighting the need for early recognition and prompt treatment.
TPP with ventricular tachycardia warrants consideration in hypokalemic paralysis among Saudis; extends sparse case reports but leaves regional incidence open.
Thyrotoxic periodic paralysis (TPP) is a potentially lethal complication of hyperthyroidism characterized by recurrent muscle weakness and hypokalemia. It has been commonly reported in non-Asian populations. Four cases were reported in Saudis so far, and one had a life-threatening arrhythmia. We describe an additional case of a 28-year-old apparently healthy Saudi male patient, who presented with acute paraparesis associated with hypokalemia (K: 2.0 mmol/L), complicated by ventricular tachycardia and cardiac arrest. He was successfully resuscitated and his hypokalemia was corrected. A diagnosis of Graves' disease associated with TPP was made. He was initially treated with carbimazole and β-blockers and then given a definitive therapy with radioactive iodine, which showed a good response. This case highlights the importance of early recognition and prompt treatment of TPP as a differential diagnosis for muscle weakness. A brief review of TPP and associated arrhythmia is included.
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Hakami et al. (2016) conducted a case report in Thyrotoxic periodic paralysis and Graves' disease (n=1). Carbimazole, beta-blockers, and radioactive iodine was evaluated. Thyrotoxic periodic paralysis in a 28-year-old male presented with severe hypokalemia (2.0 mmol/L) and ventricular tachycardia, which was successfully managed with antithyroid therapy.
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