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先天性巨结肠:以黏膜下神经干大小为标准的诊断方法

Congenital megacolon: diagnosis using size of sub-mucosal nerve trunk as a criteria.

作者信息

Sangkhathat Surasak, Tadtayathikom Kamolnate, Patrapinyokul Sakda, Mitarnun Winyou

机构信息

Department of Surgery, Faculty of Medicine, Prince of Songkla University, Thailand.

出版信息

J Med Assoc Thai. 2002 Feb;85(2):250-5.

Abstract

UNLABELLED

Cholinergic hyperinnervation in submucosa of aganglionic segment of Hirschsprung's disease has been described. However, objective measurement of the nerve fibers was insufficiently reported.

OBJECTIVES

To study the amount and size of hypertrophic submucosal nerve trunks in the aganglionic segment of Hirschsprung's disease, semiquantitatively and evaluate the possibility of using the size as objective diagnostic criteria.

MATERIAL AND METHOD

Thirteen specimens from aganglionic segments from Hirschsprung's disease and six specimens from the age-matched control subjected without colonic innervation disorders were studied with the S-100 immunohistochemical technic. The submucosal nerve trunks were counted per ten HPF and measured in width, semiquantitatively. Fiber sizes were stratified into small (<20 micrometers), medium (20-40 micrometers), and large (>40 micrometers). Maximum fiber size in each specimen was also recorded.

RESULTS

Average density of submucosal nerve trunk in the aganglionic segment and the control were 12.5 and 3.4 fibers per ten HPF, respectively. The large nerve trunks were detected in 12 of 13 aganglionic specimens and none was detected in the controls. The maximum fiber size in aganglionic segments was 78.2 micrometers, compared to 24.1 micrometers in the control group. The sensitivity and specificity to set the presence of hypertrophic nerve trunk, larger than 40 micrometers as a diagnostic criteria for Hirschsprung's disease were 92.3 and 100 per cent, respectively. The data suggest the use of this size as an objective diagnostic criterion, which may be valuable in rectal suction biopsy specimens.

摘要

未标注

已描述了先天性巨结肠症无神经节段黏膜下层的胆碱能神经纤维过度支配情况。然而,对神经纤维的客观测量报道不足。

目的

半定量研究先天性巨结肠症无神经节段肥厚的黏膜下神经干的数量和大小,并评估将其大小用作客观诊断标准的可能性。

材料与方法

采用S-100免疫组化技术,研究了13例先天性巨结肠症无神经节段的标本和6例年龄匹配、无结肠神经支配障碍的对照标本。每10个高倍视野计数黏膜下神经干数量,并半定量测量其宽度。将纤维大小分为小(<20微米)、中(20 - 40微米)、大(>40微米)三类。还记录了每个标本中的最大纤维大小。

结果

无神经节段和对照组黏膜下神经干的平均密度分别为每10个高倍视野12.5条和3.4条纤维。13例无神经节标本中有12例检测到粗大神经干,对照组未检测到。无神经节段的最大纤维大小为78.2微米,而对照组为24.1微米。将直径大于40微米的肥厚神经干的存在作为先天性巨结肠症的诊断标准,其敏感性和特异性分别为92.3%和100%。数据表明将此大小用作客观诊断标准,这在直肠吸引活检标本中可能有价值。

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