[Inflammatory myalgic syndrome and muscular mitochondrial abnormalities: 4 cases].

G Serratrice, V Daumen-Legré, P Lafforgue, H Perrier, P C Acquaviva, J F Pellissier, C Desnuelle
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Abstract

Histologic and biochemical anomalies of muscle mitochondria were identified in four patients with predominantly rhizomelic myalgia clinically suggestive of an inflammatory disease but inconsistent biologic evidence of inflammation. This clinical pattern was initially suggestive of atypical polymyalgia rheumatica and could not be ascribed to any other disease. To explain this combination of anomalies, several hypotheses can be put forward, including coincidence, aging, and nonspecific mitochondrial anomalies resulting from immunologic or inflammatory disease. The speculation that these patients have an autonomous syndrome cannot be outruled but should be considered with caution. A therapeutic trial with coenzyme Q is under way.

【炎性肌痛综合征及肌肉线粒体异常4例】。
在4例以根状肌痛为主的患者中发现了肌肉线粒体的组织学和生化异常,临床提示炎症性疾病,但炎症的生物学证据不一致。这种临床模式最初提示非典型多肌痛风湿病,不能归因于任何其他疾病。为了解释这种异常组合,可以提出几种假设,包括巧合、衰老和由免疫或炎症性疾病引起的非特异性线粒体异常。不能排除这些患者患有自主综合症的猜测,但应谨慎考虑。一项使用辅酶Q的治疗试验正在进行中。
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