Thyrotoxic Periodic Paralysis in a 20-Year-Old Nigerian Male

Anyanwu Ac, M. Ca, Nwazor Eo, Oputa Rn
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Abstract

Background: Thyrotoxic Periodic Paralysis (TPP) is a rare complication of hyperthyroidism characterised by hypokalaemia and recurrent episodes of muscle weakness. Increased awareness will promote early diagnosis and prompt treatment of the condition. Objective: To highlight an uncommon case of TPP in a Nigerian male with normokalaemia on presentation. Case: A 20-year-old male patient on treatment for hyperthyroidism (Grave’s disease) who was referred to the endocrine clinic on account of recurrent episodes of acute symmetrical painful lower limb muscle weakness. He had experienced a total of 5 episodes approximately 2-3 months apart with each attack lasting between 10-36 h there was a positive history of strenuous activities preceding each attack. Limb pain was relieved by analgesics and weakness resolved spontaneously without any specific medications after 2-3 days. Investigations revealed elevated T3 and T4 (212.3 ng/ml and 18.3 μg/ml respectively), reduced TSH (<0.1 mIU/ ml), low-normal serum potassium (3.6 mmol/L) on presentation and hypokalaemia (2.5 mmol/L) during an episode and hypocalcaemia (2.0 mmol/L). He was placed on 30 mg of carbimazole, propranolol 120 mg in divided doses and low dose oral potassium chloride. He showed remarkable response to treatment with reduction in the frequency of attacks and eventual resolution of symptoms.
尼日利亚20岁男性甲状腺毒性周期性麻痹一例
背景:甲状腺毒性周期性麻痹(TPP)是一种罕见的甲状腺机能亢进并发症,其特征是低钾血症和反复发作的肌肉无力。提高对该病的认识将促进该病的早期诊断和及时治疗。目的:强调一个不常见的病例TPP在尼日利亚男性与正常钾血症的表现。病例:一名20岁男性患者治疗甲状腺机能亢进(格雷夫斯病),因急性对称性疼痛性下肢肌无力反复发作而被转介至内分泌门诊。患者共经历5次发作,每次发作间隔约2-3个月,每次发作持续10-36小时,每次发作前均有剧烈活动史。肢体疼痛经镇痛剂缓解,2-3天后无力自行消退,无需任何特殊药物。调查显示T3和T4升高(分别为212.3 ng/ml和18.3 μg/ml), TSH降低(<0.1 mIU/ ml),出现时血清钾低于正常水平(3.6 mmol/L),发作时低钾(2.5 mmol/L)和低钙(2.0 mmol/L)。卡马唑30毫克,心得安120毫克,分次服用,小剂量口服氯化钾。他对治疗表现出显著的反应,发作频率减少,症状最终缓解。
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