Goebel H H, Kohlschütter A, Lenard H G
Clin Neuropathol. 1982;1(2):73-82.
Based on typical clinical and morphologic features, biopsy findings in an 18-year-old girl afflicted with mucolipidosis IV are reported. She had had corneal clouding since early childhood, psychomotor retardation resulting in severe mental impairment, and pigmentary retinopathy. Biopsies of skeletal muscle, rectum, skin, and lymphocytes revealed by light microscopy increased activity of acid phosphatase and by electron microscopy, membranous and vacuolar lysosomal residual bodies in numerous cells, including striated muscle fibers and lymphocytes. An unidentified lipid was encountered by means of thin-layer chromatography in the muscle biopsy. Thus, skeletal muscle, rectum, skin, and lymphocytes are equally suitable for in vivo morphologic diagnosis of mucolipidosis IV.
基于典型的临床和形态学特征,报告了一名患有黏脂贮积症IV型的18岁女孩的活检结果。她自幼年起就有角膜混浊,精神运动发育迟缓导致严重智力障碍,以及色素性视网膜炎。骨骼肌、直肠、皮肤和淋巴细胞的活检通过光学显微镜检查显示酸性磷酸酶活性增加,通过电子显微镜检查显示在包括横纹肌纤维和淋巴细胞在内的许多细胞中有膜性和空泡状溶酶体残余小体。在肌肉活检中通过薄层色谱法发现了一种不明脂质。因此,骨骼肌、直肠、皮肤和淋巴细胞同样适用于黏脂贮积症IV型的体内形态学诊断。