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Indexed/Abstracted in: BIOSIS Previews, EMBASE, Scopus, Emerging Sources Citation Index
Online ISSN 1827-1812
Division of Endocrinology and Metabolism University of Iowa Hospital, Iowa City, USA
Thyrotoxic hypokalemic periodic paralysis (HPP) is a rare disease, mostly found in Asians. A case of periodic paralysis triggered by too much levothyroxine (L-T4) administration in a hypothyroid patient is presented. The patient was admitted to the hospital with severe generalized muscle weakness and inability to walk. Prior to admission, her dose of L-T4 had been gradually increased because she was complaining of fatigue. She was severely hypokalemic on admission (K-1.9 mEq/L) and the thyroid panel was consistent with iatrogenic hyperthyroidism due to too much L-T4 (low TSH and high free T4). She recovered from the acute episodes with KCl infusion. Long term treatment included correcting of the hyperthyroid state, propranolol and spironolactone. Diagnosis of thyrotoxic HPP should be considered in patients presenting with severe muscle weakness due to hypokalemia especially that the typical hyperthyroidism symptoms are not obvious.