Ceuterick C, Martin J J
J Neurol Sci. 1984 Aug;65(2):179-91. doi: 10.1016/0022-510x(84)90082-0.
Updated figures from our reports on electron microscopy of skin or conjunctival biopsies include 256 patients, mostly suffering from lysosomal diseases. Significant morphological data supportive of the diagnosis and additional to enzyme assay (when and if an assay is available for the disorder) were discovered in 95% of the cases. Equivocal or negative data amounted to 5%. The present paper deals with some metabolic disorders which had not been fully dealt with in our previous publications and with an extension of the indications of skin biopsies: adult form and atypical variants of ceroid-lipofuscinoses, galactosialidosis, mucolipidosis IV, infantile neuroaxonal dystrophy, Lafora's disease, cardiomyopathy with generalized accumulation of intermediate filaments and congenital hypomyelination neuropathy. A comparison between biopsy and autopsy material in storage diseases shows that the storage of inclusions does not remain limited to one cell type or to one tissue even if no clinical signs are detectable. This ubiquitous character of the storage can be used for diagnostic purposes. On the other hand, the membrane-bound inclusions are not necessarily similar in all cell types and the search for characteristic features can be difficult in adult patients. Finally it is evident that skin biopsies can be used in other conditions than lysosomal disorders. The applicability of this procedure to other diseases needs further exploratory work.
我们关于皮肤或结膜活检组织电镜检查报告的最新数据涵盖256例患者,其中大多数患有溶酶体疾病。在95%的病例中发现了支持诊断且酶测定(若该疾病有可用的酶测定方法)之外的重要形态学数据。模棱两可或阴性数据占5%。本文讨论了一些在我们之前的出版物中未充分涉及的代谢紊乱疾病,以及皮肤活检适应证的扩展:类脂褐质沉积症的成人型和非典型变体、半乳糖唾液酸贮积症、黏脂贮积症IV型、婴儿型神经轴索性营养不良、拉福拉病、伴有中间丝广泛蓄积的心肌病以及先天性髓鞘形成低下性神经病。储存疾病活检材料与尸检材料的比较表明,即使没有可检测到的临床症状,内含物的储存也不限于一种细胞类型或一种组织。这种储存的普遍性特征可用于诊断目的。另一方面,膜结合内含物在所有细胞类型中不一定相似,在成年患者中寻找特征性特征可能很困难。最后很明显,皮肤活检可用于溶酶体疾病以外的其他情况。该程序对其他疾病的适用性需要进一步的探索性研究。