Chief of Neurology, Hines VA Hospital and Neurology Residency Program Director, Loyola University Medical Center Hines, IL, USA.
Front Neurol. 2011 Aug 5;2:49. doi: 10.3389/fneur.2011.00049. eCollection 2011.
Muscle diseases can constitute a large variety of both acquired and hereditary disorders. Myopathies in systemic disease results from several different disease processes including endocrine, inflammatory, paraneoplastic, infectious, drug- and toxin-induced, critical illness myopathy, metabolic, and myopathies with other systemic disorders. Patients with systemic myopathies often present acutely or sub acutely. On the other hand, familial myopathies or dystrophies generally present in a chronic fashion with exceptions of metabolic myopathies where symptoms on occasion can be precipitated acutely. Most of the inflammatory myopathies can have a chance association with malignant lesions; the incidence appears to be specifically increased only in patients with dermatomyositis. In dealing with myopathies associated with systemic illnesses, the focus will be on the acquired causes. Management is beyond the scope of this chapter. Prognosis is based upon the underlying cause and, most of the time, carries a good prognosis. In order to approach a patient with suspected myopathy from systemic disease, a stepwise approach is utilized.
肌肉疾病可以包括多种获得性和遗传性疾病。系统性疾病中的肌病是由多种不同的疾病过程引起的,包括内分泌、炎症、副肿瘤、感染、药物和毒素诱导、危重病肌病、代谢性肌病以及伴有其他系统性疾病的肌病。系统性肌病患者常表现为急性或亚急性发病。另一方面,家族性肌病或肌营养不良通常以慢性方式出现,但代谢性肌病除外,其症状有时可能会急性发作。大多数炎症性肌病可能与恶性病变有关;这种关联的发生率似乎仅在皮肌炎患者中特异性增加。在处理与系统性疾病相关的肌病时,重点将放在获得性病因上。治疗超出了本章的范围。预后取决于潜在病因,大多数情况下预后良好。为了从系统性疾病的角度来处理疑似肌病的患者,可采用逐步的方法。