Kimura S, Kobayashi T, Amemiya F, Sasaki Y, Misugi N
Department of Pediatrics, Yokohama City University School of Medicine, Japan.
Brain Dev. 1990;12(6):779-83. doi: 10.1016/s0387-7604(12)80006-4.
The diaphragm muscle pathology in four patients with Fukuyama type congenital progressive muscular dystrophy (FCMD) was reported. In the diaphragm muscle fibers of three patients aged more than 14 years exhibiting chronic respiratory failure, a lot of electron dense lesions, which varied in size but did not extend over the whole length of the muscle fibers, and a marked increase in mitochondria were observed as well as the dystrophic changes. The dense lesions, consisting of electron dense fibrillary material comparable to Z-band materials in electron density, seemed to be due to Z-band disruption leading to streaming and/or large aggregations of Z-band materials. No mitochondria or other microorganelles were found in these dense lesions. These findings are thought not to be specific to FCMD, but seem to reflect diaphragm muscle fatigue, because, there were no such lesions in the diaphragm muscle of a 2-year-old infant not exhibiting chronic respiratory failure or in muscle at other sites in all patients.
报告了4例福山型先天性进行性肌营养不良(FCMD)患者的膈肌病理学情况。在3例年龄超过14岁且出现慢性呼吸衰竭的患者的膈肌纤维中,观察到许多电子致密病变,其大小各异,但未延伸至肌纤维全长,同时伴有线粒体显著增多以及营养不良性改变。这些致密病变由电子密度与Z带物质相当的电子致密纤维状物质组成,似乎是由于Z带破坏导致Z带物质的流注和/或大量聚集所致。在这些致密病变中未发现线粒体或其他细胞器。这些发现被认为并非FCMD所特有,而是似乎反映了膈肌疲劳,因为在未出现慢性呼吸衰竭的2岁婴儿的膈肌中以及所有患者其他部位的肌肉中均未发现此类病变。