A Pediatric Case of Refractory Torsades de Pointes in Autoimmune Hypothyroidism.

JCEM case reports Pub Date : 2024-07-15 eCollection Date: 2024-07-01 DOI:10.1210/jcemcr/luae124
Sri Nikhita Chimatapu, Jessica L Schachter, Anjan S Batra, Rachel Sirignano, Erin R Okawa
{"title":"A Pediatric Case of Refractory Torsades de Pointes in Autoimmune Hypothyroidism.","authors":"Sri Nikhita Chimatapu, Jessica L Schachter, Anjan S Batra, Rachel Sirignano, Erin R Okawa","doi":"10.1210/jcemcr/luae124","DOIUrl":null,"url":null,"abstract":"<p><p>Hypothyroidism can have a significant impact on cardiac contractility, vascular resistance, blood pressure, and cardiac rhythm. Ventricular arrhythmias induced by hypothyroidism are infrequently reported, especially in pediatric cases. A 15-year-old girl with autoimmune hypothyroidism experienced pulseless ventricular arrhythmias on 2 separate occasions because of nonadherence to levothyroxine medication. Subsequent investigations revealed an <i>SCN5A</i> mutation associated with Brugada syndrome. A loop recorder captured polymorphic ventricular tachycardia (PMVT), specifically Torsades de Pointes during her second event. Both arrhythmias were addressed only after stabilizing her thyroid hormone levels with replacement therapy. Although rare, patients with uncontrolled hypothyroidism may present with ventricular arrhythmias, particularly PMVT. The cornerstone of treatment for hypothyroidism-induced ventricular arrhythmia is thyroid replacement therapy. The identification of an <i>SCN5A</i> mutation unmasked by overt hypothyroidism emphasizes the need for a comprehensive cardiac evaluation in patients with hypothyroidism being assessed for PMVT.</p>","PeriodicalId":73540,"journal":{"name":"JCEM case reports","volume":"2 7","pages":"luae124"},"PeriodicalIF":0.0000,"publicationDate":"2024-07-15","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11247166/pdf/","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"JCEM case reports","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1210/jcemcr/luae124","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2024/7/1 0:00:00","PubModel":"eCollection","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0

Abstract

Hypothyroidism can have a significant impact on cardiac contractility, vascular resistance, blood pressure, and cardiac rhythm. Ventricular arrhythmias induced by hypothyroidism are infrequently reported, especially in pediatric cases. A 15-year-old girl with autoimmune hypothyroidism experienced pulseless ventricular arrhythmias on 2 separate occasions because of nonadherence to levothyroxine medication. Subsequent investigations revealed an SCN5A mutation associated with Brugada syndrome. A loop recorder captured polymorphic ventricular tachycardia (PMVT), specifically Torsades de Pointes during her second event. Both arrhythmias were addressed only after stabilizing her thyroid hormone levels with replacement therapy. Although rare, patients with uncontrolled hypothyroidism may present with ventricular arrhythmias, particularly PMVT. The cornerstone of treatment for hypothyroidism-induced ventricular arrhythmia is thyroid replacement therapy. The identification of an SCN5A mutation unmasked by overt hypothyroidism emphasizes the need for a comprehensive cardiac evaluation in patients with hypothyroidism being assessed for PMVT.

查看原文
分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
一例自身免疫性甲状腺功能减退症难治性阵发性抽搐的儿科病例
甲状腺功能减退症会对心脏收缩力、血管阻力、血压和心律产生重大影响。甲状腺功能减退症诱发室性心律失常的报道并不多见,尤其是在儿童病例中。一名患有自身免疫性甲状腺功能减退症的 15 岁女孩因未按时服用左甲状腺素药物,两次出现无脉性室性心律失常。随后的检查发现,她的 SCN5A 基因突变与 Brugada 综合征有关。环路记录仪捕捉到了多形性室性心动过速(PMVT),特别是在第二次发作时出现了 Torsades de Pointes。这两次心律失常都是在使用替代疗法稳定甲状腺激素水平后才得到控制的。尽管罕见,但未得到控制的甲状腺功能减退症患者可能会出现室性心律失常,尤其是 PMVT。治疗甲减引起的室性心律失常的基石是甲状腺替代疗法。发现明显的甲状腺功能减退会掩盖 SCN5A 基因突变,这强调了对接受 PMVT 评估的甲状腺功能减退患者进行全面心脏评估的必要性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 去求助
来源期刊
自引率
0.00%
发文量
0
期刊最新文献
Empagliflozin-induced Myopathy. Severe, Symptomatic Hypercalcemia Secondary to PTH-secreting Pancreatoblastoma. A Case of Enfortumab Vedotin-Associated Diabetic Ketoacidosis With Severe Insulin Resistance in a Nondiabetic Woman. Acquired 11β-hydroxylase Deficiency by Inhaled Etomidate and its Analogues: A Mimic of Congenital Adrenal Hyperplasia. Aldosterone-producing Multiple Micronodules With Several Different KCNJ5 Pathogenic Variants.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
现在去查看 取消
×
提示
确定
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术
文献互助 智能选刊 最新文献 互助须知 联系我们:info@booksci.cn
Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。
Copyright © 2023 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1