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[皮肌炎和多发性肌炎:临床特点与治疗]

[Dermatomyositis and polymyositis: clinical aspects and treatment].

作者信息

Hachulla E

机构信息

Service de Médecine Interne, Hôpital Claude-Huriez, Centre Hospitalier et Universitaire, 59037 Lille Cedex, France.

出版信息

Ann Med Interne (Paris). 2001 Nov;152(7):455-64.

Abstract

Dermatomyositis and polymyositis are the two major idiopathic inflammatory myopathies. The Bohan and Peter's criteria are still useful despite the probably different pathogenesis of the two myopathies. Cutaneous manifestations of dermatomyositis include heliotrope rash and Gottron's papules. The heliotrope rash, with or without edema, in a distribution involving periorbital skin is very suggestive of the diagnosis. Papules may be found overlying the "kneedle" of the hand or the elbows, knees, feet. Periungueal erythema with telangiectasis were characteristic but not pathognomonic. Scalp involvement is common. Skin lesions of dermatomyositis may precede the development of the myopathy and may persist after the control of the myositis. Some patients have an amyopathic dermatomyositis with normal muscle-enzyme, magnetic resonance scan and muscle biopsy. Muscle disease affects the proximal muscles, is generally symmetrical and symptoms are fatigue, weakness and sometimes myalgia. Proximal dysphagia reflects an involvement of striated muscle of the pharynx or proximal esophagus. Camptocormia reflects a severe involvement of paravertebral muscle. Other systemic features may be seen: pulmonary involvement (mostly interstitial pneumonitis and hypoventilation), arthralgias or arthritis, cardiac involvement, vasculatis and calcinosis particularly in children or adolescents with dermatomyositis. Malignant disease is associated with idiopathic inflammatory myopathies with a frequency of approximatively 10 to 15% in dermatomyositis and 5 to 10% in polymyositis and is strongly correlated with age, more than 50% of the patient over 65 years old were found to have a cancer. In the absence of malignant disease, the mainstay therapy for dermatomyositis and polymyositis is systemic corticosteroids (mostly 1mg/kg). In the lake of response or high dose dependance, intravenous immunoglobulins or immunosuppressive drugs like methotrexate or azathioprine may be discuss. Cyclophosphamide show some effectiveness in interstitial pneumonitis. Cyclosporin might be effective in children, less in adults. The efficacy of tacrolimus, mycophenolate mofetil, leflunomide and anti-TNF therapy need some prospective studies to determine if there are of value in idiopathic inflammatory myositis.

摘要

皮肌炎和多发性肌炎是两种主要的特发性炎性肌病。尽管这两种肌病的发病机制可能不同,但博汉和彼得的标准仍然有用。皮肌炎的皮肤表现包括向阳疹和Gottron丘疹。伴有或不伴有水肿的向阳疹,分布于眶周皮肤,对诊断有很强的提示作用。丘疹可能出现在手部“指关节”或肘部、膝部、足部上方。甲周红斑伴毛细血管扩张具有特征性,但并非特异性表现。头皮受累很常见。皮肌炎的皮肤病变可能在肌病出现之前就已存在,并且在肌炎得到控制后可能持续存在。一些患者患有无肌病性皮肌炎,其肌肉酶、磁共振扫描和肌肉活检均正常。肌肉疾病影响近端肌肉,通常呈对称性,症状包括疲劳、无力,有时还有肌痛。近端吞咽困难反映了咽部或近端食管的横纹肌受累。脊柱前凸反映了椎旁肌的严重受累。还可能出现其他全身表现:肺部受累(主要是间质性肺炎和通气不足)、关节痛或关节炎、心脏受累、血管炎和钙质沉着,尤其是在患有皮肌炎的儿童或青少年中。恶性疾病与特发性炎性肌病相关,在皮肌炎中的发生率约为10%至15%,在多发性肌炎中的发生率为5%至10%,并且与年龄密切相关,超过65岁的患者中超过50%被发现患有癌症。在没有恶性疾病的情况下,皮肌炎和多发性肌炎的主要治疗方法是全身使用糖皮质激素(大多为1mg/kg)。在治疗无效或对高剂量有依赖的情况下,可以考虑静脉注射免疫球蛋白或使用免疫抑制药物,如甲氨蝶呤或硫唑嘌呤。环磷酰胺对间质性肺炎有一定疗效。环孢素对儿童可能有效,对成人效果较差。他克莫司、霉酚酸酯、来氟米特和抗TNF治疗的疗效需要一些前瞻性研究来确定它们在特发性炎性肌炎中是否有价值。

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