他汀类药物治疗5年后出现的免疫介导的坏死性肌病。

Nathan G DeRon, Francis Fischer, Dylan Lopez, Elizabeth C Brewer
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摘要

免疫介导的坏死性肌病(IMNM)是一种越来越常见和严重的疾病,其自身抗体攻击肌肉纤维,导致临床显着的肌肉无力,疲劳和肌痛。认识IMNM的临床表现是困难的,但必要的,因为快速干预可以降低发病率。我们报告一例53岁的女性,他汀类药物治疗引起IMNM,血清学检测证实抗3-羟基-3-甲基戊二酰辅酶a还原酶抗体存在。患者停止他汀类药物治疗,给予患者一剂甲基强的松龙和持续的霉酚酸盐治疗。随后,她的肌肉无力和肌痛症状缓慢改善。对于临床医生来说,重要的是要意识到他汀类药物治疗可能产生的后果,因为这些药物在医学界通常被认为是良性的。临床医生也应该意识到他汀类药物诱导的肌病可能在他汀类药物治疗期间的任何时候发生。这种情况并不一定与开始新的他汀类药物有关,正如本病例所证明的那样,患者在出现症状之前一直在接受慢性他汀类药物治疗。持续的临床医生教育和建立关于这种疾病的医学知识基金对于使临床医生认识到这种疾病并及时采取行动以减少患者发病率和改善结果至关重要。
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Immune-Mediated Necrotizing Myopathy Manifesting after Five Years of Statin Therapy.

Immune-mediated necrotizing myopathy (IMNM) is an increasingly common and serious condition in which autoantibodies attack muscle fibers causing clinically significant muscle weakness, fatigue, and myalgias. Recognizing the clinical presentation of IMNM is difficult but necessary, as rapid intervention decreases morbidity. We present a case of a 53-year-old female with IMNM induced by statin therapy with confirmed anti-3-hydroxy-3-methylglutaryl coenzyme A reductase antibodies present on serologic testing. The patient's statin therapy was halted, and the patient was provided with one dose of methylprednisolone and ongoing therapy with mycophenolate. She showed subsequent slow improvements in her muscle weakness and myalgias. It is important for clinicians to be aware of the possible consequences of statin therapy, as these drugs are generally regarded as benign in the medical community. Clinicians should also be aware that statin-induced myopathy can occur at any time during statin therapy. The condition does not necessarily correlate with beginning a new statin medication, as demonstrated in this case in which the patient was on chronic statin therapy before developing symptoms. Continued clinician education and building the fund of medical knowledge regarding this disease are vital to enable clinicians to recognize this disease and act promptly to reduce patient morbidity and improve outcomes.

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