Takagaki Kosuke, Osawa Satoshi, Ito Tatsuhiro, Iwaizumi Moriya, Hamaya Yasushi, Tsukui Hiroe, Furuta Takahisa, Wada Hidetoshi, Baba Satoshi, Sugimoto Ken
Kosuke Takagaki, Tatsuhiro Ito, Moriya Iwaizumi, Yasushi Hamaya, Ken Sugimoto, First Department of Medicine, Hamamatsu University School of Medicine, Hamamatsu 431-3192, Japan.
World J Gastroenterol. 2016 May 7;22(17):4416-20. doi: 10.3748/wjg.v22.i17.4416.
An inverted Meckel's diverticulum is a rare gastrointestinal congenital anomaly that is difficult to diagnose prior to surgery and presents with anemia, abdominal pain, or intussusception. Here, we report the case of 57-year-old men with an inverted Meckel's diverticulum, who was preoperatively diagnosed using double-balloon enteroscopy. He had repeatedly experienced epigastric pain for 2 mo. Ultrasonography and computed tomography showed intestinal wall thickening in the pelvis. Double-balloon enteroscopy via the anal route was performed for further examination, which demonstrated an approximately 8-cm, sausage-shaped, submucosal tumor located approximately 80 cm proximal to the ileocecal valve. A small depressed erosion was observed at the tip of this lesion. Forceps biopsy revealed heterotopic gastric mucosa. Thus, the patient was diagnosed with an inverted Meckel's diverticulum, and single-incision laparoscopic surgery was performed. This case suggests that an inverted Meckel's diverticulum should be considered as a differential diagnosis for a submucosal tumor in the ileum. Balloon-assisted enteroscopy with forceps biopsy facilitate a precise diagnosis of this condition.
倒位梅克尔憩室是一种罕见的胃肠道先天性异常,术前难以诊断,表现为贫血、腹痛或肠套叠。在此,我们报告一例57岁男性倒位梅克尔憩室患者,其术前通过双气囊小肠镜检查得以确诊。他反复上腹部疼痛2个月。超声检查和计算机断层扫描显示盆腔肠壁增厚。经肛门途径进行双气囊小肠镜检查以进一步检查,发现距回盲瓣约80 cm处有一个约8 cm长的香肠形黏膜下肿瘤。在该病变顶端观察到一个小的凹陷性糜烂。钳取活检显示异位胃黏膜。因此,该患者被诊断为倒位梅克尔憩室,并接受了单切口腹腔镜手术。该病例表明,倒位梅克尔憩室应被视为回肠黏膜下肿瘤的鉴别诊断之一。带钳取活检的气囊辅助小肠镜有助于对此病进行精确诊断。