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[组织化学在神经肌肉疾病分类中的贡献]

[Contribution of histochemistry to the classification of neuromuscular diseases].

作者信息

Scarlato G

出版信息

Riv Istochim Norm Patol. 1975;19(1-4):76-94.

PMID:1233715
Abstract

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after the first muscle biopsy performed on man by Bilroth in 1965, histological study of the muscle has been linked to out of date patterns of interpretation most of them without any importance for clinical diagnosis.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.

摘要

1865年比尔罗特首次对人体进行肌肉活检后的很长一段时间里,肌肉组织学研究一直与过时的解释模式相关联,其中大多数对临床诊断并无重要意义。肌肉研究中组织化学技术的应用是最近才引入的,因此在过去15年里,已经有可能收集到大量对许多神经肌肉疾病临床诊断非常重要的数据。首先通过帕迪库拉和赫尔曼的肌原纤维ATP酶反应将肌纤维分为不同类型,这使得病理解释成为可能,从而在组织学和肌电图结果之间建立了特定的关联。此外,在研究线粒体酶活性以及糖原分解和合成酶时使用不同的组织酶学方法,促进了更精细的纤维分型系统。由于冷冻切片技术的发展,上述方法在实验室日常工作中变得易于操作。冷冻切片机的使用能够更好地保存肌肉组织,从而得出更准确的诊断解释,尤其是在形态学方面。纤维分型研究揭示了许多改变:单纤维类型萎缩、I型或II型优势、类型分组、单纤维类型肥大等等,这不仅使临床医生能够进行更精细的病因学解释,而且能做出比过去更精确的诊断。在单根肌纤维研究中使用上述组织酶学方法已经取得了重要成果。英美作者为我们提供了许多重要术语,以指出单根肌纤维内酶分布的改变:蛀蚀状、靶纤维、杆状体、中央核、肌膜下泡。其中一些改变在特定的神经肌肉疾病中出现,从疾病分类学角度来看,仍然是这些疾病唯一的鉴别特征。毫无疑问,可以断言在过去15年里,在人体肌肉组织研究中使用组织化学方法已经实现了与组织化学时代之前使用的截然不同的神经肌肉疾病分类。由于组织化学,随之而来的诊断和治疗优势在神经病学这一重要领域取得了非常有趣的成果。

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