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多因素低钙血症表现为肌病的罕见病例报告

An Unusual Presentation of Multifactorial Hypocalcemia as Myopathy: A Case Report.

作者信息

Aloke Aloke, Singh Komal

机构信息

Department of Medicine, Tata Main Hospital, Dhanbad, IND.

Department of Obstetrics and Gynecology, Tata Main Hospital, Dhanbad, IND.

出版信息

Cureus. 2025 Jul 7;17(7):e87434. doi: 10.7759/cureus.87434. eCollection 2025 Jul.

DOI:10.7759/cureus.87434
PMID:40717880
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC12296704/
Abstract

Hypocalcemia is a common metabolic disturbance with a broad spectrum of clinical presentations, ranging from asymptomatic laboratory findings to severe, life-threatening complications. While neuromuscular irritability is a well-known feature, myopathy as a primary presentation is rare and often under-recognized. We report the case of a 45-year-old female with type 2 diabetes and hypertension who presented with progressive lower limb weakness and generalized body aches. She had a recent history of an abdominal skin abscess and had received blood transfusions without calcium correction. On examination, she demonstrated significant proximal muscle weakness and elevated serum creatine kinase levels. Laboratory investigations revealed severe hypocalcemia (serum calcium 4.5 mg/dL), low vitamin D, and inappropriately low-normal parathyroid hormone (PTH) levels. ECG showed QTc prolongation and anteroseptal injury pattern. A diagnosis of hypocalcemic myopathy secondary to idiopathic hypoparathyroidism, compounded by vitamin D deficiency, sepsis, and transfusion-related citrate load, was made. The patient was treated with intravenous calcium gluconate, vitamin D supplementation, and antibiotics. Her muscle strength gradually improved with normalization of calcium levels. She was discharged on oral calcium and calcitriol, and showed near-complete recovery at the two-week follow-up. This report highlights the importance of considering hypocalcemia in patients presenting with myopathy. Multiple contributing factors can coexist and exacerbate calcium deficiency in these patients. Early recognition and prompt correction are essential to prevent long-term neuromuscular complications.

摘要

低钙血症是一种常见的代谢紊乱,临床表现范围广泛,从无症状的实验室检查结果到严重的、危及生命的并发症。虽然神经肌肉兴奋性增加是一个众所周知的特征,但以肌病作为主要表现较为罕见,且常常未被充分认识。我们报告一例45岁患有2型糖尿病和高血压的女性患者,她出现进行性下肢无力和全身酸痛。她近期有腹部皮肤脓肿病史,接受过输血且未进行钙补充。体格检查时,她表现出明显的近端肌无力以及血清肌酸激酶水平升高。实验室检查显示严重低钙血症(血清钙4.5mg/dL)、维生素D水平低以及甲状旁腺激素(PTH)水平处于不适当的低正常范围。心电图显示QTc延长和前间隔损伤模式。诊断为特发性甲状旁腺功能减退继发的低钙性肌病,合并维生素D缺乏、脓毒症和输血相关的枸橼酸盐负荷。患者接受了静脉注射葡萄糖酸钙、补充维生素D以及抗生素治疗。随着钙水平恢复正常,她的肌肉力量逐渐改善。她出院时服用口服钙剂和骨化三醇,在两周随访时显示几乎完全康复。本报告强调了在出现肌病的患者中考虑低钙血症的重要性。多种促成因素可能同时存在并加重这些患者的钙缺乏。早期识别和及时纠正对于预防长期神经肌肉并发症至关重要。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9562/12296704/b0854035147b/cureus-0017-00000087434-i01.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9562/12296704/b0854035147b/cureus-0017-00000087434-i01.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9562/12296704/b0854035147b/cureus-0017-00000087434-i01.jpg

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