Polymyalgia Rheumatica, an Age-Related Rheumatic Disease

Z. Schmidt, G. Poór
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Abstract

Polymyalgia rheumatica (PMR) is an age-related chronic inflammatory disease with rheumatic features at the fore. In addition to the high-grade systemic inflammation, it is characterized by typical “polymyalgic” musculoskeletal symptoms, including diffuse and severe pain and prolonged morning stiffness of the shoulder girdle, pelvic girdle, and neck. PMR is a member of the so-called giant cell arteritis complex; however, in spite of the marked systemic inflammation in PMR, the local vasculitis process aborts. The pathological background is synovitis, with a predominant inflammation of the extra-articular synovial structures. Synovitis of PMR is mild, transient, and non-erosive. Distal musculoskeletal symptoms are also observed but are more variable and less recognizable than the predominant proximal polymyalgic syndrome. PMR often overlaps with elderly-onset seronegative arthritides, elderly-onset rheumatoid arthritis, late-onset seronegative spondylarthritis, and the RS3PE1 syndrome. Although glucocorticoids are the cornerstone of PMR therapy, considerable hope is attached to tocilizumab, an IL-6 receptor inhibitor.
多肌痛风湿病,一种与年龄相关的风湿病
风湿性多肌痛(PMR)是一种与年龄相关的慢性炎症性疾病,以风湿病为主要特征。除了高度全身性炎症外,其特征是典型的“多肌痛”肌肉骨骼症状,包括弥漫性和剧烈疼痛以及肩带、骨盆带和颈部的长时间晨僵。PMR是所谓巨细胞动脉炎复合体的一员;然而,尽管PMR有明显的全身性炎症,但局部血管炎过程终止。病理背景为滑膜炎,主要是关节外滑膜结构的炎症。PMR的滑膜炎是轻微的,短暂的,非侵蚀性的。远端肌肉骨骼症状也可观察到,但与主要的近端多肌痛综合征相比,变化更大,更难以识别。PMR常与老年性血清阴性关节炎、老年性类风湿关节炎、迟发性血清阴性脊柱炎和RS3PE1综合征重叠。尽管糖皮质激素是PMR治疗的基石,但IL-6受体抑制剂tocilizumab的前景仍不容乐观。
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