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伪装的甲状腺功能亢进症:一例新发房颤和急性可逆性麻痹病例

Hyperthyroidism in Disguise: A Case of New-Onset Atrial Fibrillation and Acute Reversible Paralysis.

作者信息

Shahid Urooj, Ashin Nusrat T, Dara Saqib I

机构信息

College of Medicine, Gulf Medical University, P. O. Box 4184, Ajman, UAE.

Department of Critical Care Medicine, Sheikh Shakhbout Medical City, P. O. Box 11001, Abu Dhabi, UAE.

出版信息

JCEM Case Rep. 2025 Aug 22;3(10):luaf193. doi: 10.1210/jcemcr/luaf193. eCollection 2025 Oct.

Abstract

Thyrotoxic periodic paralysis (TPP) is a rare and potentially life-threatening disorder characterized by transient muscle weakness due to hypokalemia in the setting of hyperthyroidism. We present a case of a 32-year-old male with no prior history of thyroid disease who developed acute, progressive paralysis of all 4 extremities. Laboratory findings revealed profound hypokalemia, hypophosphatemia, and elevated lactate. Electrocardiography showed new-onset atrial fibrillation with a rapid ventricular response. Thyroid function tests confirmed hyperthyroidism, and further evaluation led to the diagnosis of Graves disease. The patient was treated with intravenous potassium and phosphorus replacement, leading to full neurological recovery within 24 hours. He was subsequently started on carbimazole for long-term thyroid hormone suppression. The occurrence of atrial fibrillation in TPP is an uncommon yet significant complication. Additionally, elevated lactate is an extremely rare finding.

摘要

甲状腺毒症性周期性瘫痪(TPP)是一种罕见且可能危及生命的疾病,其特征为在甲状腺功能亢进的情况下,因低钾血症导致短暂性肌肉无力。我们报告一例32岁男性病例,该患者既往无甲状腺疾病史,却出现了急性、进行性的四肢瘫痪。实验室检查结果显示严重低钾血症、低磷血症以及乳酸水平升高。心电图显示新发房颤伴快速心室率。甲状腺功能检查证实为甲状腺功能亢进,进一步评估后诊断为格雷夫斯病。患者接受了静脉补钾和补磷治疗,24小时内神经功能完全恢复。随后他开始服用卡比马唑以长期抑制甲状腺激素。TPP中出现房颤是一种罕见但重要的并发症。此外,乳酸水平升高是极其罕见的发现。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3906/12371528/065201d5be70/luaf193f1.jpg

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