Abraham S C, DeNofrio D, Loh E, Minda J M, Tomaszewski J E, Pietra G G, Reynolds C
Department of Pathology and Laboratory Medicine, University of Pennsylvania Medical Center, Philadelphia, USA.
Hum Pathol. 1998 Aug;29(8):876-82. doi: 10.1016/s0046-8177(98)90460-9.
Desmin myopathy is a rare idiopathic disorder characterized by abnormal aggregates of desmin-type intermediate filaments, which affects cardiac and skeletal muscle, and rarely the intestinal smooth muscle. We report a 42-year-old woman with atrial fibrillation and progressive restrictive cardiomyopathy. Left ventricular biopsy, cardiac explant, and subsequent autopsy study of skeletal muscle revealed cytoplasmic granulo-filamentous inclusions that were continuous with Z-lines and were immunoreactive for desmin filaments both at the light immunohistochemical and electron microscopic level. In addition, we report the presence of characteristic inclusions within the smooth muscle of intramural coronary blood vessels. This is the first description of desmin inclusions within vascular smooth muscle, and underscores the systemic nature of this rare myopathy.
结蛋白肌病是一种罕见的特发性疾病,其特征是结蛋白型中间丝异常聚集,累及心肌和骨骼肌,很少累及肠道平滑肌。我们报告一名42岁患有心房颤动和进行性限制性心肌病的女性。左心室活检、心脏外植体以及随后的骨骼肌尸检研究显示,细胞质中有颗粒状细丝状包涵体,这些包涵体与Z线连续,在光免疫组织化学和电子显微镜水平上对结蛋白丝均呈免疫反应性。此外,我们报告在壁内冠状动脉血管平滑肌内存在特征性包涵体。这是血管平滑肌内结蛋白包涵体的首次描述,并强调了这种罕见肌病的全身性。