Libânio Diogo, Brandão Catarina, Pimentel-Nunes Pedro, Dinis-Ribeiro Mário
Gastroenterology Department, Portuguese Oncology Institute of Porto, Porto, Portugal.
GE Port J Gastroenterol. 2017 Nov;24(6):285-287. doi: 10.1159/000479234. Epub 2017 Aug 10.
Anti-angiogenic therapy with bevacizumab, an inhibitor of vascular endothelial growth factor, is commonly used in metastatic colorectal cancer and is rarely associated with gastrointestinal perforation, perforation being more frequent in the primary tumor site or at the anastomotic level. We present the case of a 64-year-old male with stage IV rectal adenocarcinoma who was on palliative chemotherapy with FOLFOX and bevacizumab. After the 4th chemotherapy cycle, our patient started fever and epigastric pain. He was hemodynamically stable, and signs of peritoneal irritation were absent. There were no alterations in the abdominal X-ray, and C-reactive protein was markedly elevated. A CT scan revealed a de novo thickness in the gastric antrum. Upper digestive endoscopy showed an ulcerated 40-mm lesion in the angulus, with a 20-mm orifice communicating with an exsudative cavity revested by the omentum. A conservative approach was decided including fasting, broad-spectrum intravenous antibiotics, and proton-pump inhibitors. Subsequent gastroduodenal series showed no contrast extravasation, allowing the resumption of oral nutrition. Esophagogastroduodenoscopy after 8 weeks showed perforation closure. Biopsies did not show neoplastic cells or infection. Although the success in the conservative management of perforation allowing the maintenance of palliative chemotherapy (without bevacizumab), the patient died after 4 months due to liver failure. The reported case shows an uncommon endoscopic finding due to a rare complication of anti-angiogenic therapy. Additionally, it reminds clinicians that a history of gastroduodenal ulcers should be actively sought before starting anti-angiogenic treatment and that suspicion for perforation should be high in these cases.
贝伐单抗是一种血管内皮生长因子抑制剂,抗血管生成疗法常用于转移性结直肠癌,很少与胃肠道穿孔相关,穿孔在原发肿瘤部位或吻合口处更为常见。我们报告一例64岁男性,患有IV期直肠腺癌,正在接受FOLFOX和贝伐单抗姑息化疗。在第4个化疗周期后,患者开始发热和上腹部疼痛。他血流动力学稳定,无腹膜刺激征。腹部X线无异常,C反应蛋白明显升高。CT扫描显示胃窦部有新发增厚。上消化道内镜检查显示胃角处有一个40毫米的溃疡性病变,有一个20毫米的开口与一个被大网膜覆盖的渗出腔相通。决定采取保守治疗方法,包括禁食、广谱静脉抗生素和质子泵抑制剂。随后的胃肠造影显示无造影剂外渗,可恢复口服营养。8周后的食管胃十二指肠镜检查显示穿孔闭合。活检未发现肿瘤细胞或感染。尽管穿孔保守治疗成功,允许维持姑息化疗(不使用贝伐单抗),但患者在4个月后因肝功能衰竭死亡。该病例报告显示了抗血管生成治疗罕见并发症导致的罕见内镜检查结果。此外,它提醒临床医生,在开始抗血管生成治疗前应积极询问胃十二指肠溃疡病史,在这些病例中对穿孔的怀疑应很高。