[组织化学对神经肌肉疾病分类的贡献]。

G Scarlato
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引用次数: 0

摘要

在Bilroth于1965年对人体进行第一次肌肉活检后的很长一段时间里,肌肉的组织学研究一直与过时的解释模式联系在一起,其中大多数对临床诊断没有任何重要性。组织化学技术在肌肉研究中的应用是最近才引入的,因此在过去的15年里,已经有可能收集到大量非常重要的数据,用于许多神经肌肉疾病的临床诊断。Padykula和Hermann首先利用肌纤维atp酶反应将肌纤维分类为不同类型,这使得病理解释能够导致组织学和肌电图结果之间的特定相关性。此外,在线粒体酶活性和糖原分解和合成酶的研究中使用不同的组织酶学方法,促进了更精细的纤维分型系统。由于低温显微切开术的发展,上述方法在实验室日常工作中变得容易操作。低温恒温器的使用,可以更好地保存肌肉组织,导致更准确的诊断解释,特别是在形态学方面。纤维分型的研究揭示了许多变化:单一纤维型萎缩,1型或2型优势,类型分组,单一纤维型肥大等,给临床医生提供了更详细的病理解释的可能性,而且比过去更精确的诊断。上述组织酶学方法在单根肌纤维的研究中取得了重要的成果。盎格鲁-撒克逊作家为我们提供了许多有意义的术语,以指出单个肌纤维内酶分布的变化:蛾食,目标纤维,棒,中央核心,肌鞘下泡。在特定的神经肌肉疾病中看到的这些改变,从医院的角度来看仍然是这些疾病的唯一区别特征。可以毫无疑问地断言,在过去的15年中,组织化学方法在人体肌肉组织研究中的使用,使得神经肌肉疾病的病区分类与组织化学时代之前使用的分类有很大不同。由于组织化学在诊断和治疗方面的优势,在神经学这一重要领域取得了非常有趣的结果。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
[Contribution of histochemistry to the classification of neuromuscular diseases].

For a long time after the first muscle biopsy performed on man by Bilroth in 1965, histological study of the muscle has been linked to out of date patterns of interpretation most of them without any importance for clinical diagnosis. The use of histochemical techniques in the study of muscle was introduced quite recently and consequently in the last 15 years it has been possible to collect an enormous amount of very important data for the clinical diagnosis of many neuromuscular disorders. The classification of muscle fibers into different types which was possible first of all using the myofibrillar ATPase reaction by Padykula and Hermann permitted pathological interpretation leading to specific correlations between histological and EMG results. Furthermore the use of different histoenzymological methods in the study of mitochondrial enzymes activity and of the enzymes for the glycogen breakdown and synthesis, promoted a more elaborate fibre typing system. Thank to the development of cryostatic microtomy, the above mentioned methods became easy to be performed in the laboratory routine work. The use of the cryostat, which allows a better preservation of muscular tissue, led to a more accurate diagnostic interpretation particularly in relation to morphology. The study of fiber typing revealed many alterations: single fiber type atrophy, type one or type two predominance, type grouping, hypertrophy of a single fiber type and so on, giving to the clinicians the possibility not only of a more elaborate pathogenetic interpretation, but also of a much more precise diagnosis than in the past. Important results have been achieved using the above mentioned histoenzymological methods in the study of the single muscle fibers. Anglo-Saxon Authors provided us with many significant terms, in order to point out alterations of the enzymes distribution within the single muscle fiber: moth eaten, target fiber, rods, central core, subsarcolemmal blebs. Some of these alterations, seen in specific neuromuscular disorders, still represent the only distinguishing feature of these disorders from the nosographic point of view. It is possible to assert without any doubts that in the last 15 years the use of histochemical methods in the study of human muscular tissue has allowed a nosografic classification of neuromuscular disorders very different from that in use before the histochemical age. Thanks to histochemistry the consequent diagnostic and therapeutic advantages have led to very interesting results in such an important field of Neurology.

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