Sheet plastination of the larynx for whole-organ histology.

Acta anatomica Pub Date : 1997-01-01 DOI:10.1159/000147914
C Sittel, H E Eckel, S Ricke, E Stennert
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引用次数: 10

Abstract

Whole organ serial sections of the larynx are recognized to improve the assessment of laryngeal pathology. The human larynx with its complex anatomy of different types of tissue with their marked differences in hardness complicate the cutting process. The methods established are either very costly, time consuming and prone to artefacts, or sections are too thick for a histological work-up. Prior decalcification causes major shrinkage, thus morphometry is not feasible. We describe a technique of sheet plastination to produce whole-organ sections which allows a full-scale histological investigation without prior decalcification. Deep-frozen larynges are cut into 4-micron-thick sections using an ordinary slicing machine. Slices are dehydrated in acetone and plastinated in Biodur E50/E7/ AE10/E700. These specimens are cut into sections of about 80 microns thickness using a diamond-wire saw. An ultra-milling device reduces the section thickness down to about 10 microns. Surface staining of different kinds like Richardson, methylene blue or Paragon yields sufficient contrast for exact diagnosis. Deplastination and consecutive paraffin-like staining is possible, but results are not yet fully satisfying. Histological sheet plastination produces almost artefact- and shrinkage-free whole-organ sections in a period of about 1 week. The technique is useful for studies of micromorphometry or tumor spread. Theoretically, application of immunohistochemical staining methods seems to be possible. This might lead to mapping the proliferation activity of laryngeal cancer as it is presented on whole-organ sections.

喉部全器官组织学的薄片塑化。
喉的整个器官序列切片被确认以改善喉病理的评估。人类喉部的解剖结构复杂,不同类型的组织在硬度上有明显的差异,这使得切割过程变得复杂。所建立的方法要么非常昂贵,耗时且容易产生人工制品,要么切片太厚而无法进行组织学检查。先前的脱钙会导致严重的收缩,因此形态测定法是不可行的。我们描述了一种薄片塑化技术,以产生整个器官切片,允许全面的组织学调查,而无需事先脱钙。用普通切片机将深冻喉切成4微米厚的切片。切片在丙酮中脱水,在Biodur E50/E7/ AE10/E700中塑化。这些标本用金刚石线锯切成约80微米厚的部分。超铣削装置将截面厚度降低到约10微米。不同种类的表面染色,如理查森、亚甲基蓝或帕拉贡染色,可以产生足够的对比,以进行准确的诊断。脱色和连续石蜡样染色是可能的,但结果尚不完全令人满意。组织学薄片塑化在大约一周的时间内产生几乎无伪影和无收缩的整个器官切片。该技术可用于显微形态学或肿瘤扩散的研究。理论上,应用免疫组织化学染色方法似乎是可能的。这可能导致绘制喉癌的增殖活动,因为它是在整个器官切片上呈现的。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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