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免疫组织化学辅助诊断先天性巨结肠病。

Immunohistochemistry as an aid in the diagnosis of Hirschsprung's disease.

作者信息

Hall C L, Lampert P W

出版信息

Am J Clin Pathol. 1985 Feb;83(2):177-81. doi: 10.1093/ajcp/83.2.177.

Abstract

The interpretation of rectal suction mucosal biopsies taken for the purpose of ruling out Hirschsprung's disease (HD) can be especially difficult in neonatal patients because of ganglion cell (GC) immaturity. Acetylcholinesterase histochemistry on frozen sections can be helpful but requires experience and may be complicated by excessive mucosal hemorrhage. The authors retrospectively have studied 27 patients, including 11 patients with HD, on whom conventionally fixed and embedded tissue was available, using an immunoperoxidase system directed against neuron-specific enolase (NSE) and S100 protein. NSE immunostaining produced intense staining of GC perikarya, greatly facilitating recognition of small immature forms. S100 immunostaining also highlighted GC as prominent negative stained cells surrounded by the positivity of Schwann cells. Both stains were helpful in demonstrating the overall pattern of microinnervation and its relationship to possible GC. The authors conclude that NSE and S100 immunostaining may facilitate interpretation of rectal mucosal biopsies when Hirschsprung's disease is being considered as a possibility.

摘要

由于神经节细胞(GC)不成熟,为排除先天性巨结肠(HD)而进行的直肠吸引黏膜活检在新生儿患者中的解读可能特别困难。冰冻切片上的乙酰胆碱酯酶组织化学检查可能会有所帮助,但需要经验,并且可能因黏膜出血过多而变得复杂。作者回顾性研究了27例患者,其中包括11例HD患者,这些患者有常规固定和包埋的组织,使用针对神经元特异性烯醇化酶(NSE)和S100蛋白的免疫过氧化物酶系统。NSE免疫染色使GC核周体产生强烈染色,极大地便于识别小的未成熟形式。S100免疫染色也将GC突出显示为被施万细胞阳性包围的明显阴性染色细胞。两种染色都有助于展示微神经支配的整体模式及其与可能的GC的关系。作者得出结论,当考虑先天性巨结肠病的可能性时,NSE和S100免疫染色可能有助于直肠黏膜活检的解读。

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