Uncovering non-autoimmune hypothyroidism: A case report of rhabdomyolysis and myocarditis mimicking acute coronary syndrome.

IF 1.3 4区 医学 Q2 MEDICINE, GENERAL & INTERNAL
Hyejin Jeon, Seunghye Lee, Sehyun Jung, Hani Jang, Se-Ho Chang, Hyun-Jung Kim
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引用次数: 0

Abstract

Rationale: Non-autoimmune hypothyroidism is a rare but significant cause of rhabdomyolysis and myocarditis, which can mimic acute coronary syndrome. Early recognition and treatment of hypothyroidism are crucial, especially in patients with chronic kidney disease (CKD), where delayed diagnosis may lead to life-threatening complications such as acute kidney injury.

Patient concerns: A 71-year-old male with diabetes, CKD stage G3aA3, and a history of chronic myelogenous leukemia presented with myalgia, anorexia, and anuria. He also reported intermittent chest pain for 1 month, progressing to severe symptoms including decreased urine output and anuria.

Diagnoses: Laboratory findings revealed acute kidney injury (serum creatinine: 12.14 mg/dL), extreme elevations in muscle enzymes (creatine kinase: 250,000 IU/L), and cardiac biomarkers (troponin-T: 543 ng/L). Initial management did not improve his condition. On day 15, thyroid function tests confirmed non-autoimmune hypothyroidism (TSH: 55.58 μIU/mL, free T4: 0.06 ng/dL).

Interventions: The patient underwent hemodialysis and conservative treatment initially, followed by levothyroxine replacement therapy on day 16.

Outcomes: Renal function, urine output, and muscle enzyme levels gradually improved after thyroid hormone supplementation. By discharge on day 40, the patient's serum creatinine decreased to 3.08 mg/dL, and hemodialysis was discontinued. At 7 months posttreatment, his renal function stabilized at CKD stage G3bA2 with normal thyroid function.

Lessons: This case highlights the importance of considering hypothyroidism in patients with unexplained rhabdomyolysis and persistent cardiac symptoms, particularly in those with CKD. Early thyroid function testing can lead to timely treatment and improved outcomes in such complex cases.

揭示非自身免疫性甲状腺功能减退:横纹肌溶解和心肌炎模拟急性冠状动脉综合征1例报告。
理由:非自身免疫性甲状腺功能减退症是一种罕见但重要的原因横纹肌溶解和心肌炎,可模仿急性冠状动脉综合征。早期识别和治疗甲状腺功能减退是至关重要的,特别是对于慢性肾脏疾病(CKD)患者,延迟诊断可能导致危及生命的并发症,如急性肾损伤。患者关注:71岁男性,糖尿病,CKD G3aA3期,有慢性髓性白血病病史,表现为肌痛、厌食、无尿。他还报告间歇性胸痛1个月,进展为严重症状,包括尿量减少和无尿。诊断:实验室结果显示急性肾损伤(血清肌酐:12.14 mg/dL),肌肉酶极度升高(肌酸激酶:250000 IU/L),心脏生物标志物(肌钙蛋白- t: 543 ng/L)。最初的治疗并没有改善他的病情。第15天,甲状腺功能检查证实非自身免疫性甲状腺功能减退(TSH: 55.58 μIU/mL,游离T4: 0.06 ng/dL)。干预措施:患者最初接受血液透析和保守治疗,第16天给予左旋甲状腺素替代治疗。结果:补充甲状腺激素后,肾功能、尿量和肌酶水平逐渐改善。出院第40天,患者血清肌酐降至3.08 mg/dL,停止血液透析。治疗后7个月,肾功能稳定在CKD G3bA2期,甲状腺功能正常。经验教训:本病例强调了在患有不明原因横纹肌溶解和持续心脏症状的患者,特别是CKD患者中考虑甲状腺功能减退的重要性。早期甲状腺功能检测可以及时治疗并改善此类复杂病例的预后。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Medicine
Medicine 医学-医学:内科
CiteScore
2.80
自引率
0.00%
发文量
4342
审稿时长
>12 weeks
期刊介绍: Medicine is now a fully open access journal, providing authors with a distinctive new service offering continuous publication of original research across a broad spectrum of medical scientific disciplines and sub-specialties. As an open access title, Medicine will continue to provide authors with an established, trusted platform for the publication of their work. To ensure the ongoing quality of Medicine’s content, the peer-review process will only accept content that is scientifically, technically and ethically sound, and in compliance with standard reporting guidelines.
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