Goulet Olivier, Salomon Julie, Ruemmele Frank, de Serres Natacha Patey-Mariaud, Brousse Nicole
Department of Pediatric Gastroenterology-Hepatology and Nutrition and Reference Center for Rare Digestive Disease, Hopital Necker-Enfants Malades, 149, Rue de Sèvres, Cédex 15, 75743 Paris, France.
Orphanet J Rare Dis. 2007 Apr 20;2:20. doi: 10.1186/1750-1172-2-20.
Intestinal epithelial dysplasia (IED), also known as tufting enteropathy, is a congenital enteropathy presenting with early-onset severe intractable diarrhea causing sometimes irreversible intestinal failure. To date, no epidemiological data are available, however, the prevalence can be estimated at around 1/50,000-100,000 live births in Western Europe. The prevalence seems higher in areas with high degree of consanguinity and in patients of Arabic origin. Infants develop within the first days after birth a watery diarrhea persistent in spite of bowel rest and parenteral nutrition. Some infants are reported to have associated choanal rectal or esophageal atresia. IED is thought to be related to abnormal enterocytes development and/or differentiation. Nonspecific punctuated keratitis was reported in more than 60% of patients. Histology shows various degree of villous atrophy, with low or without mononuclear cell infiltration of the lamina propria but specific histological abnormalities involving the epithelium with disorganization of surface enterocytes with focal crowding, resembling tufts. Several associated specific features were reported, including abnormal deposition of laminin and heparan sulfate proteoglycan (HSPG) in the basement membrane, increased expression of desmoglein and ultrastructural changes in the desmosomes, and abnormal distribution of alpha2beta1 integrin adhesion molecules. One model of transgenic mice in which the gene encoding the transcription factor Elf3 is disrupted have morphologic features resembling IED. Parental consanguinity and/or affected siblings suggest an autosomal recessive transmission but the causative gene(s) have not been yet identified making prenatal diagnosis unavailable. Some infants have a milder phenotype than others but in most patients, the severity of the intestinal malabsorption even with enteral feeding make them totally dependent on daily long-term parenteral nutrition with a subsequent risk of complications. IED becomes an indication for intestinal transplantation, while timing of referral for it is crucial before the onset of severe complications.
肠上皮发育异常(IED),也称为簇状肠病,是一种先天性肠病,表现为早发性严重顽固性腹泻,有时会导致不可逆的肠衰竭。迄今为止,尚无流行病学数据,不过据估计,在西欧,其患病率约为每50000 - 100000例活产中有1例。在近亲结婚程度高的地区以及阿拉伯裔患者中,患病率似乎更高。婴儿在出生后的头几天就会出现水样腹泻,尽管进行了肠道休息和肠外营养,腹泻仍会持续。据报道,一些婴儿伴有后鼻孔闭锁、直肠闭锁或食管闭锁。IED被认为与肠上皮细胞发育和/或分化异常有关。超过60%的患者报告有非特异性点状角膜炎。组织学显示不同程度的绒毛萎缩,固有层单核细胞浸润少或无,但上皮有特定的组织学异常,表现为表面肠上皮细胞紊乱,局部聚集,类似绒毛簇。还报告了一些相关的特定特征,包括基底膜中层粘连蛋白和硫酸乙酰肝素蛋白聚糖(HSPG)的异常沉积、桥粒芯糖蛋白表达增加和桥粒超微结构改变,以及α2β1整合素黏附分子分布异常。一种编码转录因子Elf3的基因被破坏的转基因小鼠模型具有类似于IED的形态学特征。父母近亲结婚和/或有患病的兄弟姐妹提示为常染色体隐性遗传,但致病基因尚未确定,因此无法进行产前诊断。一些婴儿的表型比其他婴儿轻,但在大多数患者中,即使进行肠内喂养,肠道吸收不良的严重程度也使他们完全依赖每日长期的肠外营养,随后有并发症风险。IED成为肠移植的指征,而在严重并发症发生之前进行转诊的时机至关重要。