We retrospectively evaluated the characteristics of adult patients admitted with thyrotoxic hypokalaemic periodic paralysis in Hong Kong. From 1984 to 1993, 45 Chinese adult patients were admitted with acute limb weakness, plasma potassium ≤ 3.5 mmol/l and thyrotoxicosis confirmed by laboratory investigations. All but one were male. Seventy-five percent of attacks occurred between 9pm and 9am. Half of the attacks occurred between July and October (49.1), most commonly in August (20). Mean ( ± SEM) plasma potassium on admission was 2.17 ± 0.08 mmol/l (range 1.1-3.5). In 15 episodes (27.3), plasma potassium on recovery exceeded 5.0 mmol/l, while in three episodes (5.5), potassium exceeded 6.0 mmol/l. No patient had a positive family history of thyrotoxic periodic paralysis. Only 28.9 had a known history of thyrotoxicosis before their first presentation with periodic paralysis. Twenty-seven (60) had clinical evidence of thyrotoxicosis. Although all were biochemically thyrotoxic, 11.4 had only a mild degree of thyrotoxicosis (suppressed thyroid-stimulating hormone, high free thyroxine, but normal free triiodothyron-ine). One quarter of the patients had a normal erythrocyte zinc concentration, indicating either a short history of thyrotoxicosis or transient thyrotoxicosis. The diagnosis of thyrotoxic hypokalaemic paralysis should always be considered in Chinese patients with acute muscle weakness, especially in young males. Absence of clinical thyrotoxicosis does not exclude the diagnosis. Plasma potassium should be monitored carefully during treatment to prevent rebound hyperkalaemia.
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