Department of Human Immunology, SA Pathology, Adelaide, Australia.
Allergy Asthma Immunol Res. 2012 Jan;4(1):52-4. doi: 10.4168/aair.2012.4.1.52. Epub 2011 Nov 10.
Acute rhabdomyolysis is a clinical and laboratory syndrome resulting from the breakdown of skeletal muscle, with the release of intracellular contents into the circulatory system, which can cause potentially lethal complications. Here, we present the case of a patient who developed acute rhabdomyolysis after consumption of meloxicam for jaw pain and experienced generalized myalgias in the context of an acute febrile illness with generalized urticaria. Further investigation indicated elevated muscle enzymes and acute renal failure. Serological analysis revealed that the patient was positive for Ross River virus (RRV) IgM. Genetic studies to detect CYP2C9 polymorphisms were negative. Meloxicam was discontinued. He responded to conservative measures within 2 weeks. Oral aspirin challenge was negative, suggesting a drug-specific effect of meloxicam rather than a class effect. Our case indicates a causative role for meloxicam and/or acute RRV in rhabdomyolysis.
横纹肌溶解症是一种由骨骼肌破裂引起的临床和实验室综合征,细胞内物质释放到循环系统中,可能导致潜在的致命并发症。在这里,我们报告了 1 例因服用美洛昔康治疗颌痛而发生横纹肌溶解症的患者,该患者在伴有全身性荨麻疹的急性发热性疾病中出现全身肌肉疼痛。进一步的检查提示肌酶升高和急性肾衰竭。血清学分析显示患者为罗河病毒(RRV)IgM 阳性。检测 CYP2C9 多态性的基因研究为阴性。停用美洛昔康后,患者在 2 周内得到缓解。口服阿司匹林激发试验为阴性,提示美洛昔康的药物特异性作用而非类效应。我们的病例表明美洛昔康和/或急性 RRV 在横纹肌溶解症中起因果作用。