Anand Priyanka, Singh Sompal, Sarin Namrata
Department of Pathology, NDMC and Hindu Rao Hospital, Malka Ganj, New Delhi, 110007, India.
J Med Case Rep. 2017 Sep 12;11(1):258. doi: 10.1186/s13256-017-1425-x.
Intestinal intussusception is the most frequent cause of small bowel obstruction in children between the ages of 2 months and 5 years and often remains idiopathic in etiology, even after surgery. On microscopic examination, in intussusception normal mucosa is noted but in a few cases heterotopic tissue can be seen. Heterotopic gastric mucosa in the small intestine is extremely rare except for its occurrence in remnants of Meckel's diverticulum. In view of the rarity of this condition, we report a case of ectopic gastric mucosa in the small intestine that was not associated with remnants of vitelline duct.
A 6-year-old boy of Indo-Aryan ethnicity from India presented with episodes of acute abdominal pain and distension with vomiting and non-passage of stools. On ultrasonography intussusception was suspected. A laparotomy was done and the ileal segment (tip of intussusception) was sent for histopathological examination. On histopathology, sections from the tip of intussusception showed extensive gastric metaplasia of the mucosa.
A definitive diagnosis of heterotopic gastric mucosa is established by histopathological examination and it is important to differentiate heterotopia, which is a developmental anomaly, from metaplasia, which is an acquired condition. Heterotopic gastric mucosa is usually clinically silent and surgical intervention can be considered in patients with complications such as gastrointestinal hemorrhage and intestinal obstruction.
肠套叠是2个月至5岁儿童小肠梗阻最常见的原因,即使在手术后,其病因通常仍为特发性。在显微镜检查中,肠套叠可见正常黏膜,但少数情况下可见异位组织。小肠异位胃黏膜极为罕见,除了在梅克尔憩室残端出现。鉴于这种情况的罕见性,我们报告一例小肠异位胃黏膜病例,该病例与卵黄管残端无关。
一名来自印度的6岁印度-雅利安族男孩出现急性腹痛、腹胀、呕吐且无排便。超声检查怀疑为肠套叠。进行了剖腹手术,并将肠套叠顶端的回肠段送去做组织病理学检查。组织病理学检查显示,肠套叠顶端的切片显示黏膜广泛胃化生。
通过组织病理学检查可明确诊断异位胃黏膜,将作为发育异常的异位与作为后天获得性情况的化生区分开来很重要。异位胃黏膜通常在临床上无症状,对于出现诸如胃肠道出血和肠梗阻等并发症的患者可考虑手术干预。