Martini Wayne A, Griffin Thomas N, Rappaport Douglas, McElhinny Megan, Querin Lauren B
Emergency Medicine, Mayo Clinic Arizona, Phoenix, USA.
Emergency Medicine, Mayo Clinic Alix School of Medicine, Phoenix, USA.
Cureus. 2024 Nov 21;16(11):e74151. doi: 10.7759/cureus.74151. eCollection 2024 Nov.
Thyrotoxic periodic paralysis (TPP) is a rare but significant complication of hyperthyroidism, characterized by episodes of muscle weakness or paralysis and associated hypokalemia. This case report details a 30-year-old Latin American male with a history of Graves' disease, presenting with acute muscle weakness and hypokalemia. The patient reported transient episodes of weakness over recent weeks, culminating in a severe episode prompting emergency evaluation. Physical examination revealed marked weakness, particularly in the lower limbs, a moderate goiter, and bilateral exophthalmos. Laboratory workup confirmed hypokalemia and uncontrolled thyrotoxicosis, with an elevated Burch-Wartofsky Point Scale score suggestive of thyroid storm. Treatment involved potassium and magnesium replacement, along with re-initiation of methimazole and propranolol, leading to significant improvement within hours. Persistent thyrotoxicosis was attributed to inconsistent medication adherence, prompting counseling on adherence strategies and discussion of more definitive treatment options. This case highlights the importance of recognizing TPP across diverse populations, emphasizes prompt management of hypokalemia and thyrotoxicosis to prevent severe complications, and underscores the critical role of patient education in chronic disease management. By contributing to the growing body of literature on TPP in non-Asian patients, this report supports the need for heightened clinical awareness of TPP in hyperthyroid patients presenting with acute muscle weakness and hypokalemia. Additionally, it emphasizes the importance of a thorough evaluation, prompt management, and patient education to prevent recurrence and achieve long-term management of Graves' disease.
甲状腺毒症性周期性瘫痪(TPP)是一种罕见但严重的甲状腺功能亢进并发症,其特征为发作性肌无力或麻痹,并伴有低钾血症。本病例报告详细介绍了一名30岁的拉丁裔男性,有格雷夫斯病病史,出现急性肌无力和低钾血症。患者报告近几周有短暂的肌无力发作,最终发展为严重发作并促使其进行急诊评估。体格检查发现明显的肌无力,尤其是下肢,中度甲状腺肿大和双侧突眼。实验室检查确诊为低钾血症和未控制的甲状腺毒症,Burch-Wartofsky积分升高提示甲状腺危象。治疗包括补钾和补镁,同时重新开始使用甲巯咪唑和普萘洛尔,数小时内即有显著改善。持续性甲状腺毒症归因于用药依从性不一致,因此对其进行了依从性策略咨询并讨论了更明确的治疗方案。本病例强调了在不同人群中识别TPP的重要性,强调及时处理低钾血症和甲状腺毒症以预防严重并发症,并强调了患者教育在慢性病管理中的关键作用。通过为非亚洲患者中关于TPP的文献积累做出贡献,本报告支持对于出现急性肌无力和低钾血症的甲状腺功能亢进患者提高对TPP的临床认识的必要性。此外,它强调了全面评估、及时处理和患者教育对于预防复发及实现格雷夫斯病长期管理的重要性。