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肌病与原发性醛固酮增多症:电子显微镜研究

Myopathy and primary aldosteronism: electronmicroscopic study.

作者信息

Atsumi T, Ishikawa S, Miyatake T, Yoshida M

出版信息

Neurology. 1979 Oct;29(10):1348-53. doi: 10.1212/wnl.29.10.1348.

Abstract

We studied two patients with myopathy and primary aldosteronism. Necrosis and vacuolation of muscle fibers were found on light microscopy. Ultrastructurally, the necrotic areas were characterized by dissolution of myofilaments with degenerative vacuoles. In muscle fibers that did not show necrosis, there were membrane-bound vacuoles, dilation of the sarcoplasmic reticulum, widening of the T-system, and a "honeycomb" appearance of T-tubules. These ultrastructural features suggest that the necrosis of muscle fibers may originate from membrane vulnerability of the sarcoplasmic reticulum and the T-system.

摘要

我们研究了两名患有肌病和原发性醛固酮增多症的患者。光镜下发现肌纤维坏死和空泡形成。超微结构上,坏死区域的特征是肌丝溶解并伴有退行性空泡。在未显示坏死的肌纤维中,存在膜结合空泡、肌浆网扩张、T 系统增宽以及 T 小管呈“蜂窝状”外观。这些超微结构特征表明肌纤维坏死可能源于肌浆网和 T 系统的膜易损性。

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