Muscle pathology in polymyalgia rheumatica: histochemical and immunohistochemical study.

S Kojima, A Takagi, M Ida, R Shiozawa
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引用次数: 4

Abstract

Immunohistochemical studies were performed on muscle biopsy specimens of polymyalgia rheumatica (PMR) to evaluate the extent of muscle and peripheral nerve involvement. The routine histochemistry revealed a mild variation of fiber size, type 2 fiber atrophy and type 2A or 2B fiber deficiency. In 63% of the PMR cases small angular fibers, pyknotic nuclear clumps or target-targetoid fibers were observed, suggesting neurogenic changes, although abnormalities were mild in degree. In immunocytochemical studies, neither major histocompatibility complex (MHC) class 1 nor class 2 products were expressed on the muscle surface membrane of PMR. But regarding intramuscular vessels, MHC class 2 products were distinctly visualized. On serial sections, combined deposits of IgG and Clq in perimysial arteries were seen in 38% of PMR. These results suggest that arteries of small caliber might be involved in immunopathological processes, causing muscle and peripheral nerve damage.
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风湿性多肌痛的肌肉病理:组织化学和免疫组织化学研究。
对风湿性多肌痛(PMR)的肌肉活检标本进行免疫组化研究,以评估肌肉和周围神经的受累程度。常规组织化学显示纤维大小轻度变化,2型纤维萎缩,2A或2B型纤维缺乏。在63%的PMR病例中,观察到小的角状纤维,固缩的核团块或靶-靶样纤维,提示神经源性改变,尽管异常程度轻微。在免疫细胞化学研究中,主要组织相容性复合体(MHC) 1类和2类产物均未在PMR的肌肉表面膜上表达。但对于肌内血管,MHC 2类产物明显可见。在连续切片上,38%的PMR患者在膜周动脉中可见IgG和Clq的联合沉积。这些结果提示小口径动脉可能参与免疫病理过程,引起肌肉和周围神经损伤。
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