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横纹肌溶解症:一名青少年男性桥本甲状腺炎的罕见表现及文献综述

Rhabdomyolysis: A Rare Presentation of Hashimoto Thyroiditis in an Adolescent Boy and Review of the Literature.

作者信息

Saroufim Rita, Alkotob Shifaa, Eugster Erica A

机构信息

Pediatric Endocrinology, Riley Hospital for Children at Indiana University Health, Indianapolis, Indiana, USA.

Pediatrics, Riley Hospital for Children at Indiana University Health, Indianapolis, Indiana, USA.

出版信息

Horm Res Paediatr. 2023;96(5):538-541. doi: 10.1159/000529673. Epub 2023 Feb 13.

Abstract

INTRODUCTION

Hypothyroidism-induced rhabdomyolysis without precipitating factors is extremely rare, particularly in pediatric patients. We describe a previously healthy adolescent boy who came to our institution with vague symptoms and was found to have rhabdomyolysis secondary to hypothyroidism due to Hashimoto thyroiditis. We also summarize previously published cases in children and adolescents.

CASE PRESENTATION

A 16-year-old boy presented to the emergency department at Riley Hospital for Children with a 2-week history of bilateral eye and lip swelling, fatigue, and slowing of speech initially attributed to angioedema. His laboratory studies were significant for acute kidney injury secondary to rhabdomyolysis. Additional evaluation revealed profound primary hypothyroidism and positive TPO antibodies. Although his free T4 was undetectable, his TSH was only 32.2 mcU/mL. He received IV hydration and thyroid replacement, and his symptoms improved after several months of treatment.

DISCUSSION

Rhabdomyolysis without any risk factors is very rare, especially in children. Our patient was not on any medications, had no family history of neuromuscular disorders, and no history of trauma, infection, or strenuous exercise. The reason behind the disproportionately mild elevation of TSH in the setting of an undetectable free T4 is unclear.

CONCLUSION

It is important for clinicians to be aware that rhabdomyolysis may be a presenting sign of severe hypothyroidism, as delay in diagnosis and treatment can be detrimental.

摘要

引言

无诱发因素的甲状腺功能减退症所致横纹肌溶解极为罕见,尤其是在儿科患者中。我们描述了一名此前健康的青少年男性,他因症状模糊前来我院就诊,结果发现患有由桥本甲状腺炎引起的甲状腺功能减退症继发横纹肌溶解。我们还总结了此前发表的儿童和青少年病例。

病例介绍

一名16岁男孩因双眼睑和唇部肿胀、疲劳及言语迟缓2周就诊于莱利儿童医院急诊科,最初这些症状被归因于血管性水肿。他的实验室检查显示因横纹肌溶解继发急性肾损伤。进一步评估发现严重原发性甲状腺功能减退症及甲状腺过氧化物酶抗体阳性。尽管其游离T4检测不到,但其促甲状腺激素仅为32.2 mU/mL。他接受了静脉补液及甲状腺替代治疗,经过数月治疗后症状改善。

讨论

无任何危险因素的横纹肌溶解非常罕见,尤其是在儿童中。我们的患者未服用任何药物,无神经肌肉疾病家族史,也无创伤、感染或剧烈运动史。在游离T4检测不到的情况下促甲状腺激素升高程度相对较轻的原因尚不清楚。

结论

临床医生应意识到横纹肌溶解可能是严重甲状腺功能减退症的一个表现体征,因为诊断和治疗延迟可能有害。

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