Matsubara S
Acta Neuropathol. 1980;50(2):91-6. doi: 10.1007/BF00692857.
Muscle biopsies from four middle-aged to elderly women with a 3--16-years' history of slowly progressive proximal muscle weakness showed non-caseating granulomas. Although two of them had clinical features suggestive of sarcoidosis, the other two had not. No distinct differences in the structural changes of these cases were noted by light or electron microscopy. The granulomas were comprised of epithelioid cells, Langhans type giant cells, lymphocytes, macrophages, and small numbers of plasma cells, monocytes, and mast cells. Some lymphocytes appeared to be transformed. The damaged muscle fibres were mostly located near the granulomas. Some of them were infiltrated by epithelioid cells, macrophages and mononuclear cells similar to lymphocytes. These cells were seen between the basement and plasma membranes of the muscle fibres. The muscle fibres showed various degenerative changes. Regeneration of muscle fibres was also observed. Filamentous intranuclear inclusions were present in two cases.
对4名患有3至16年缓慢进展性近端肌无力病史的中老年女性进行肌肉活检,结果显示有非干酪样肉芽肿。其中两名患者具有结节病的临床特征,而另外两名则没有。通过光学显微镜或电子显微镜观察,这些病例的结构变化没有明显差异。肉芽肿由上皮样细胞、朗汉斯型巨细胞、淋巴细胞、巨噬细胞以及少量浆细胞、单核细胞和肥大细胞组成。一些淋巴细胞似乎发生了转化。受损的肌纤维大多位于肉芽肿附近。其中一些被上皮样细胞、巨噬细胞和类似于淋巴细胞的单核细胞浸润。这些细胞出现在肌纤维的基底膜和质膜之间。肌纤维呈现出各种退行性变化。还观察到了肌纤维的再生。两例出现丝状核内包涵体。