Shimotake Takashi, Tomiyama Hideki, Aoi Shigeyoshi, Iwai Naomi
Division of Surgery, Children's Research Hospital, Kyoto Prefectural University of Medicine, Kyoto, Japan.
J Pediatr Surg. 2003 May;38(5):698-701. doi: 10.1016/jpsu.2003.50186.
BACKGROUND/PURPOSE: Recent studies have found that Hirschsrung's disease is caused by diverse genomic abnormalities. To clarify whether these pathogenic variations influence the distribution and function of enteric ganglia, the authors studied the morphology of the macroscopic and microscopic transitional zone in Hirschsprung's disease with reference to the type of genetic mutation.
In 120 patients with Hirschsprung's disease, the location and morphology of the gut caliber change were recorded, and the enteric nervous system was investigated histologically using biopsy specimens. The DNA sequences of all the RET/GDNF/NTN and SOX10 coding regions were determined using the direct DyeDeoxy Terminator Cycle method.
In RET mutation carriers, the gut caliber change was almost identical to the histologic transition in cases of short segment aganglionosis, whereas these were markedly dissociated in cases exhibiting extensive aganglionosis. In contrast, SOX10 mutation carriers had a very long histologic transition and exhibited no caliber change.
The type of genetic mutation responsible for Hirschsprung's disease influences the postnatal distribution and function of enteric ganglia. The data on discrepancy between macroscopic and microscopic transitions may enable us to concentrate the sites of the leveling biopsy more accurately especially in cases of long type intestinal aganglionosis carrying RET gene mutation.
背景/目的:近期研究发现,先天性巨结肠病由多种基因组异常引起。为阐明这些致病变异是否影响肠神经节的分布和功能,作者参照基因突变类型,研究了先天性巨结肠病中宏观和微观过渡区的形态。
对120例先天性巨结肠病患者记录肠管管径变化的位置和形态,并使用活检标本进行肠神经系统组织学研究。采用直接染料脱氧终止循环法测定所有RET/GDNF/NTN和SOX10编码区的DNA序列。
在RET突变携带者中,短段无神经节症病例的肠管管径变化与组织学过渡几乎相同,而在广泛无神经节症病例中,二者明显分离。相比之下,SOX10突变携带者有很长的组织学过渡,且无管径变化。
导致先天性巨结肠病的基因突变类型影响肠神经节的出生后分布和功能。宏观与微观过渡差异的数据可能使我们能够更准确地集中水平活检部位,尤其是在携带RET基因突变的长型肠无神经节症病例中。