Kimura S
Department of Pediatrics, Yokohama City University School of Medicine.
No To Hattatsu. 1991 Jan;23(1):20-5.
Ultrastructural pathology on sweat gland epithelium was studied in various neurodegenerative disorders; neuronal ceroid-lipofuscinosis (NCL), Lafora disease, mucopolysaccharidosis, GM1 gangliosidosis, Nieman-Pick disease, Fabry disease, Krabbe disease and metachromatic leukodystrophy (MLD). Every disease had its own characteristic inclusions in sweat gland epithelium. Curvilinear profiles and fingerprint patterns were seen in NCL, but there were no morphological differences among late infantile, early juvenile and juvenile types. On the other hand, the granular matrix was characteristic of the infantile type. The presence of specific inclusions in a 23-year-old female carrier with Fabry disease indicated that a skin biopsy was one of the useful methods to detect a female carrier. In MLD and Krabbe disease, there were disease specific inclusions in sweat gland epithelium. These results indicate that the sweat glands should be investigated when a skin biopsy is performed for the diagnosis of neurodegenerative diseases.
在各种神经退行性疾病中研究了汗腺上皮的超微结构病理学,包括神经元蜡样脂褐质沉积症(NCL)、拉福拉病、黏多糖贮积症、GM1神经节苷脂贮积症、尼曼-匹克病、法布里病、克拉伯病和异染性脑白质营养不良(MLD)。每种疾病在汗腺上皮中都有其独特的包涵体。在NCL中可见曲线轮廓和指纹图案,但晚期婴儿型、早期青少年型和青少年型之间没有形态学差异。另一方面,颗粒状基质是婴儿型的特征。在一名23岁的法布里病女性携带者中存在特定包涵体,这表明皮肤活检是检测女性携带者的有用方法之一。在MLD和克拉伯病中,汗腺上皮中有疾病特异性包涵体。这些结果表明,在进行皮肤活检以诊断神经退行性疾病时,应检查汗腺。