A Case of Anti-3-hydroxy-3-methylglutaryl-coenzyme A Reductase Myopathy Associated With Advanced Cervical Carcinoma.

IF 1.6 4区 医学 Q4 ONCOLOGY Anticancer research Pub Date : 2023-10-01 DOI:10.21873/anticanres.16668
Arnaud Saillant, Mathilde Rasclard, Jean-Baptiste Gaume, Odile Souchaud, Matthieu Bainaud
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Abstract

Background: Necrotizing autoimmune myopathy is characterized by skeletal muscle weakness and is frequently associated with cancer. Absence of treatment can lead to severe muscular atrophy but initial symptoms may be insidious and delay the diagnosis. Here, we describe the case of a 70-year-old woman who was diagnosed with mnti-3-hydroxy-3-methylglutaryl-coenzyme A reductase myopathy during chemotherapy course for cervical cancer.

Case report: A 70-year-old woman received chemotherapy for an advanced cervical carcinoma. She had no other relevant medical history and did not take statins. During the treatment she presented muscle weakness and myalgia. Biological tests showed elevated creatine phosphokinase level (3750 IU/l) and anti-3-hydroxy-3-methylglutaryl-coenzyme A reductase antibodies were detected in the serum. The electroneuromyogram showed short myotonic bursts in the upper limbs, with a myogenic appearance. A muscle biopsy was performed and confirmed the diagnosis of necrotizing autoimmune myopathy. The patient showed improvements after treatment with intravenous immunoglobulin and corticosteroid therapy. Then, the patient was successfully treated with subcutaneous methotrexate, which controlled the disease and demonstrated its value as maintenance treatment.

Conclusion: This case highlights the importance of screening for rare myopathies in patients suffering from cancer with myalgias and muscle weakness and the importance of electroneuromyogram and magnetic resonance imaging in the early onset of symptoms to make the correct diagnosis.

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一例与晚期宫颈癌相关的抗-3-羟基-3-甲基戊二酰辅酶A还原酶肌病。
背景:坏死性自身免疫性心肌病以骨骼肌无力为特征,常与癌症相关。缺乏治疗可能导致严重的肌肉萎缩,但最初的症状可能是隐蔽的,并推迟诊断。在此,我们描述了一例70岁的女性,她在癌症化疗过程中被诊断为mnti-3-羟基-3-甲基戊二酰辅酶a还原酶肌肉病。病例报告:一位70岁的妇女接受了晚期宫颈癌的化疗。她没有其他相关病史,也没有服用他汀类药物。在治疗过程中,她出现了肌肉无力和肌痛。生物测试显示,血清中检测到肌酸激酶水平升高(3750IU/l)和抗3-羟基-3-甲基戊二酰辅酶A还原酶抗体。肌电图显示上肢出现短暂的强直性肌张力爆发,表现为肌源性。进行了肌肉活检,确认诊断为坏死性自身免疫性肌病。患者在静脉注射免疫球蛋白和皮质类固醇治疗后表现出改善。随后,患者成功地接受了皮下甲氨蝶呤治疗,控制了疾病,并证明了其作为维持治疗的价值。结论:该病例强调了筛查癌症伴肌痛和肌肉无力患者罕见肌病的重要性,以及神经肌电和磁共振成像在早期症状发生中做出正确诊断的重要性。
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来源期刊
Anticancer research
Anticancer research 医学-肿瘤学
CiteScore
3.70
自引率
10.00%
发文量
566
审稿时长
2 months
期刊介绍: ANTICANCER RESEARCH is an independent international peer-reviewed journal devoted to the rapid publication of high quality original articles and reviews on all aspects of experimental and clinical oncology. Prompt evaluation of all submitted articles in confidence and rapid publication within 1-2 months of acceptance are guaranteed. ANTICANCER RESEARCH was established in 1981 and is published monthly (bimonthly until the end of 2008). Each annual volume contains twelve issues and index. Each issue may be divided into three parts (A: Reviews, B: Experimental studies, and C: Clinical and Epidemiological studies). Special issues, presenting the proceedings of meetings or groups of papers on topics of significant progress, will also be included in each volume. There is no limitation to the number of pages per issue.
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