Yi Ga Young, Lee Jeong Kyong, Lee Huisong, Yi Sun Young, Park SangHui
Taehan Yongsang Uihakhoe Chi. 2022 May;83(3):680-686. doi: 10.3348/jksr.2021.0041. Epub 2021 Dec 11.
Intraluminal duodenal diverticulum (IDD) is a rare congenital abnormality, consisting of a sac-like mucosal lesion in the duodenum. Cases of IDD can present with gastrointestinal bleeding, duodenal obstruction, or pancreatitis. Here, we report a rare case of a 25-year-old female presenting with IDD complicated by duodeno-duodenal intussusception and recurrent pancreatitis. The diagnosis was based on findings from radiologic examinations (CT and MRI), upper gastrointestinal series (barium swallow), and gastroduodenofiberscopy. Laparoscopic excision of the presumed duodenal duplication was performed. The subsequent histopathologic evaluation of the excised sac revealed normal mucosa on both sides, but the absence of a proper muscle layer confirmed the diagnosis of IDD. Radiologic detection of a saccular structure in the second portion of the duodenum can indicate IDD with duodeno-duodenal intussusception as the lead point.
十二指肠腔内憩室(IDD)是一种罕见的先天性异常,由十二指肠内的囊状黏膜病变组成。IDD病例可表现为胃肠道出血、十二指肠梗阻或胰腺炎。在此,我们报告一例罕见病例,一名25岁女性,患有IDD并伴有十二指肠-十二指肠套叠和复发性胰腺炎。诊断基于放射学检查(CT和MRI)、上消化道造影(吞钡)以及胃十二指肠纤维内镜检查结果。对推测的十二指肠重复畸形进行了腹腔镜切除。随后对切除的囊进行组织病理学评估,结果显示两侧黏膜正常,但缺乏正常肌层,从而确诊为IDD。十二指肠第二部出现囊状结构的放射学检测结果可提示以十二指肠-十二指肠套叠为起始点的IDD。