Mónus Z, Konyár E, Szabó L
Virchows Arch B Cell Pathol. 1977 Dec 30;26(2):159-73. doi: 10.1007/BF02889545.
Morphologic and histochemical studies have been performed at light and electron microscopic level on needle-liver biopsy specimens, circulating blood lymphocytes and fibroblast cultures from patients with mannosidosis. The findings demonstrated generalized storage phenomena of varying degrees in the various tissues examined. Histochemical findings were in agreement with the biochemical nature of the stored material. Enzyme histochemical methods indicated storage in the lysosomes, at least in the hepatocytes. The ultrastructural appearance of mannosidosis in itself has but a limited diagnostic significance since the morphology and distribution of vacuoles have characteristics in common with other storage diseases. Repeated liver biopsy disclosed extensive storage in the hepatic tissue. However, the progression of the disease was not accompanied by severe mechanical destruction or microcirculatory disturbances.
对甘露糖苷贮积症患者的肝脏穿刺活检标本、循环血淋巴细胞和成纤维细胞培养物进行了光镜和电镜水平的形态学和组织化学研究。结果表明,在所检查的各种组织中均存在不同程度的广泛性贮积现象。组织化学结果与所贮存物质的生化性质相符。酶组织化学方法显示,至少在肝细胞中,贮存发生在溶酶体中。甘露糖苷贮积症本身的超微结构表现诊断意义有限,因为空泡的形态和分布与其他贮积病有共同特征。重复肝脏活检显示肝组织中有广泛的贮积。然而,疾病进展并未伴有严重的机械性破坏或微循环障碍。