Takakura Kazuki, Kajihara Mikio, Sasaki Shigemasa, Nagano Tomohisa, Ohta Arihito, Ikegami Masahiro, Eto Ken, Kashiwagi Hideyuki, Yanaga Katsuhiko, Arihiro Seiji, Kato Tomohiro, Tajiri Hisao
Case Rep Gastroenterol. 2011 May;5(2):308-14. doi: 10.1159/000329171. Epub 2011 May 28.
Neurofibromatosis type I (NF1) is one of the most common inheritable disorders and is associated with an increased risk of gastrointestinal stromal tumours (GISTs). However, the predominant location of these lesions in the small bowel makes them difficult to diagnose. We report the successful use of balloon enteroscopy in conjunction with conventional methods for clinical diagnosis of jejunal GISTs in a 70-year-old man with NF1 who presented with melaena. The importance of screening NF1 patients for GISTs and the complementary role of balloon enteroscopy with capsule endoscopy in such diagnoses is discussed.
I型神经纤维瘤病(NF1)是最常见的遗传性疾病之一,与胃肠道间质瘤(GIST)风险增加相关。然而,这些病变在小肠的主要位置使其难以诊断。我们报告了在一名70岁患有NF1且出现黑便的男性患者中,成功使用气囊小肠镜结合传统方法对空肠GIST进行临床诊断的情况。讨论了对NF1患者进行GIST筛查的重要性以及气囊小肠镜与胶囊内镜在此类诊断中的互补作用。