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十二指肠闭锁合并“苹果皮样”小肠且成纤维细胞生长因子-10或成纤维细胞生长因子受体2IIIb无缺失:1例报告

Duodenal atresia associated with "apple peel" small bowel without deletion of fibroblast growth factor-10 or fibroblast growth factor receptor 2IIIb: report of a case.

作者信息

Tatekawa Yukihiro, Kanehiro Hiromichi, Nakajima Yoshiyuki

机构信息

Department of Surgery, Nara Medical University, Kashihara, Nara 634-8522, Japan.

出版信息

Surg Today. 2007;37(5):430-3. doi: 10.1007/s00595-006-3415-2. Epub 2007 Apr 30.

Abstract

We report a case of duodenal membranous atresia associated with "apple peel" small bowel in a baby girl. The patient's mother and sibling had also undergone surgery for duodenal atresia. Familial duodenal atresia is sometimes the result of genetic, inherited abnormalities. Fibroblast growth factor (FGF) receptor 2IIIb (Fgfr2b) and Fgf10 are known regulatory molecules relevant to mesenchymal-epithelial interactions. The involvement of the Fgf10/Fgfr2b pathway in the pathogenesis of intestinal atresia are related to tissue-specific transcription factors, which regulate the expression of Fgf10 according to the organ system and the stage of gestation. Furthermore, a spontaneous somatic mutation or a point mutation of Fgf10 early in development would result in a genetic mosaic pattern. Fluorescent in situ hybridization did not show homozygous or heterozygous deletion of the Fgf10 or Fgfr2b gene in this case. It is necessary to study the occurrence of duodenal atresia in posterity and investigate the deletion of the Fgfr2b or Fgf10 genes if possible.

摘要

我们报告了一例患有“苹果皮”样小肠的女婴十二指肠膜状闭锁病例。该患者的母亲和兄弟姐妹也因十二指肠闭锁接受了手术。家族性十二指肠闭锁有时是遗传、遗传性异常的结果。成纤维细胞生长因子(FGF)受体2IIIb(Fgfr2b)和Fgf10是已知的与间充质-上皮相互作用相关的调节分子。Fgf10/Fgfr2b途径在肠道闭锁发病机制中的参与与组织特异性转录因子有关,这些转录因子根据器官系统和妊娠阶段调节Fgf10的表达。此外,发育早期Fgf10的自发体细胞突变或点突变会导致遗传镶嵌模式。在该病例中,荧光原位杂交未显示Fgf10或Fgfr2b基因的纯合或杂合缺失。有必要研究后代中十二指肠闭锁的发生情况,并尽可能调查Fgfr2b或Fgf10基因的缺失情况。

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