Petchasuwan C, Pintong J
Institute of Pathology, Ministry of Public Health, Bangkok, Thailand.
J Med Assoc Thai. 2000 Nov;83(11):1402-9.
Hirschsprung's disease is a disease of congenital abnormalities characterized by absence of the enteric ganglion cell of the colon. To make a definite diagnosis, biopsy of the aganglionic zones of colon is required. A specimen from submucosal biopsy of the colon is very small and difficult to identify submucosal ganglion cells. Our study reports an immunohistochemical technique to detect submucosal ganglion cells. Six antineural markers, peripherin, cathepsin D, PGP 9.5, synaptophysin, chromogranin and S-100 protein, were used. The best antibody for the detection of submucosal ganglion cells in our study was peripherin. The additional measurement of nerve fiber caliber using S-100 protein staining is a valuable aid in the diagnosis of Hirschsprung's disease. It can be applied to the suction submucosal biopsy in a patient suspected of having Hirschsprung's disease, therefore, the complicated full thickness colonic and rectal biopsy can be avoided.
先天性巨结肠症是一种以结肠肠神经节细胞缺失为特征的先天性异常疾病。要做出明确诊断,需要对结肠无神经节区域进行活检。结肠黏膜下活检的标本非常小,难以识别黏膜下神经节细胞。我们的研究报告了一种检测黏膜下神经节细胞的免疫组织化学技术。使用了六种抗神经标志物,即外周蛋白、组织蛋白酶D、PGP 9.5、突触素、嗜铬粒蛋白和S-100蛋白。在我们的研究中,用于检测黏膜下神经节细胞的最佳抗体是外周蛋白。使用S-100蛋白染色额外测量神经纤维直径对先天性巨结肠症的诊断有重要帮助。它可应用于疑似先天性巨结肠症患者的吸引黏膜下活检,因此可以避免复杂的全层结肠和直肠活检。