Department of Gastroenterology, Graduate School of Medicine, The University of Tokyo, Hongo 7-3-1, Bunkyo-Ku, Tokyo, 113-8655, Japan.
Department of Plastic and Reconstructive Surgery, Graduate School of Medicine, The University of Tokyo Hongo, Hongo 7-3-1, Bunkyo-Ku, Tokyo, 113-8655, Japan.
Clin J Gastroenterol. 2024 Oct;17(5):883-890. doi: 10.1007/s12328-024-02021-x. Epub 2024 Jul 17.
Intestinal lymphangiectasia (IL) is a protein-losing enteropathy (PLE) that occasionally leads to gastrointestinal bleeding (GIB). We encountered a 41-year-old female with a 9-year history of duodenal IL with PLE and GIB that progressively worsened. Despite a diet, supplemented with medium-chain triglycerides, antiplasmin therapy, oral corticosteroids, octreotides, sirolimus, and repeated endoscopic hemostasis, her symptoms remained uncontrolled, leading to blood transfusion dependence. Lymphangiography revealed significant leakage from abnormal abdominal lymph vessels into the duodenal lumen. The patient subsequently underwent an abdominal-level lymphaticovenous anastomosis combined with local venous ligation. This approach resulted in a dramatic improvement and sustained resolution of both the PLE and GIB. More than 6 months after surgery, the patient remained free of symptoms and blood transfusion dependence.
肠淋巴管扩张症(IL)是一种蛋白丢失性肠病(PLE),偶尔会导致胃肠道出血(GIB)。我们遇到一位 41 岁女性,9 年来患有十二指肠 IL 和 PLE,GIB 逐渐加重。尽管饮食中补充了中链甘油三酯、抗纤溶治疗、口服皮质类固醇、奥曲肽、西罗莫司和反复内镜止血,但她的症状仍未得到控制,导致需要输血。淋巴管造影显示异常腹部淋巴管有大量漏液进入十二指肠腔。随后,患者接受了腹部淋巴管静脉吻合术联合局部静脉结扎术。该方法显著改善了 PLE 和 GIB,并持续缓解。手术后 6 个月以上,患者无任何症状,也无需输血。