Pathology of chronic constipation in pediatric and adult coloproctology.

W. Meier-Ruge, E. Bruder
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引用次数: 70

Abstract

In colonic motility disorders, a pathohistological diagnosis based solely on formalin-fixed gut is often inconclusive. Classical histological techniques or immunohistochemistry represent a static staining. In contrast, native tissue submitted to enzyme histochemistry provides functional information about the effectiveness of the cellular performance. Routinely, a complementary set of reactions is performed and includes acetylcholinesterase (AChE), lactic and succinic dehydrogenase, as well as nitroxide synthase reactions. In this monograph, the whole spectrum of different anomalies of the colonic wall is illustrated in a systematic fashion: Hirschsprung's disease is characterized by an increase in AChE activity of parasympathetic nerve fibers of the rectosigmoid. In ultrashort Hirschsprung's disease, only enzyme histochemistry renders a reliable diagnosis possible in biopsies of the anal ring. Aganglionosis of the musculus corrugator cutis ani shows a localized increase of AChE activity in nerve fibers, similar to Hirschsprung's disease, not detectable in conventional histology. Immaturity, hypoganglionosis and neuronal dysganglionosis can be clearly recognized in dehydrogenase reactions. Enzyme histochemical reactions are complemented by picrosirius red staining for assessment of the collagen texture of the muscularis propria. Absence or intertenial interruption of the continuous connective tissue layer between circular and longitudinal muscle of the muscularis propria has been termed aplastic or atrophic desmosis, respectively. Many of the entities described are also observed in adults. Atrophic hypoganglionosis or atrophic desmosis with loss of the myenteric plexus connective tissue fascia is implied as a frequent cause of chronic constipation in adults. The essential contribution of a functional histopathological technique towards a reliable diagnosis of gut dysfunction in native tissue is extensively demonstrated in great detail in more than two hundred figures.
儿童和成人结肠直肠慢性便秘的病理。
在结肠运动障碍中,仅基于福尔马林固定肠道的病理组织学诊断通常是不确定的。经典的组织学技术或免疫组织化学代表静态染色。相比之下,原生组织提交酶组织化学提供了有关细胞性能有效性的功能信息。通常,一组互补的反应被执行,包括乙酰胆碱酯酶(AChE),乳酸和琥珀酸脱氢酶,以及氮氧化物合酶反应。在这本专著中,以系统的方式说明了结肠壁不同异常的整个频谱:巨结肠病的特征是直肠乙状结肠副交感神经纤维乙酰胆碱酯酶活性的增加。在超短巨结肠病中,只有酶组织化学才能在肛门环活检中提供可靠的诊断。皱襞肌皮肤神经节病表现为神经纤维中乙酰胆碱酯酶活性的局部增加,类似于先天性巨结肠病,在常规组织学中未被检测到。脱氢酶反应可以清楚地识别不成熟、神经节减少症和神经节异常症。酶组织化学反应辅以小天狼星红染色来评估固有肌层的胶原结构。固有肌层的圆肌和纵肌之间的连续结缔组织层的缺失或间隔中断分别被称为再生或萎缩韧带。所描述的许多实体也在成人中观察到。萎缩性神经节减少症或萎缩性韧带粘连伴肌丛结缔组织筋膜丧失被认为是成人慢性便秘的常见原因。功能性组织病理学技术对天然组织中肠道功能障碍的可靠诊断的重要贡献在200多张图中得到了广泛的详细证明。
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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