Shimura Takaya, Kataoka Hiromi, Sasaki Makoto, Kubota Eiji, Shiraki Shigehiro, Matsusako Kei, Nakayama Yoshihide, Mizoshita Tsutomu, Mizushima Takashi, Joh Takashi
Department of Gastroenterology and Metabolism, Nagoya City University Graduate School of Medical Sciences, Nagoya.
Intern Med. 2008;47(23):2029-31. doi: 10.2169/internalmedicine.47.1357. Epub 2008 Dec 1.
Inflammatory fibroid polyp (IFP) is a rare benign tumor originating from the submucosa of the gastrointestinal tract. Most are found in the stomach, with only one previous case reported in the rectum. IFPs are typically larger than 1 cm in diameter and present symptoms. Colonoscopic examination of an asymptomatic 66-year-old man revealed a small submucosal tumor, 3 mm in diameter, in the rectum. The lesion was completely resected by endoscopic submucosal dissection (ESD) and was histopathologically diagnosed as IFP. We report herein a very rare rectal IFP that could be treated and diagnosed with ESD.
炎性纤维瘤性息肉(IFP)是一种罕见的起源于胃肠道黏膜下层的良性肿瘤。大多数发生在胃,之前仅有1例发生于直肠的报道。IFP直径通常大于1cm且有症状表现。对一名66岁无症状男性进行结肠镜检查时,发现直肠有一个直径3mm的小黏膜下肿瘤。该病变通过内镜黏膜下剥离术(ESD)完整切除,经组织病理学诊断为IFP。我们在此报告一例非常罕见的可通过ESD进行治疗和诊断的直肠IFP。