Leite Júlio S, Tralhão José Guilherme, Manso António, Fernandes Miguel, Cunha Inês, Amaro Pedro
Serviço de Cirurgia Geral, Centro Hospitalar e Universitário de Coimbra, Coimbra, Portugal.
Serviço de Gastrenterologia, Centro Hospitalar e Universitário de Coimbra, Coimbra, Portugal.
GE Port J Gastroenterol. 2020 Apr;27(3):185-191. doi: 10.1159/000503010. Epub 2019 Oct 16.
Most patients with familial adenomatous polyposis (FAP) will develop duodenal polyps and 5% progress to cancer. Those with Spigelman stage IV have a 36% risk of cancer at 10 years. Endoscopic surveillance is necessary with local ablation for early disease. Unresectable duodenal disease and severe dysplasia are an indication for prophylactic radical surgery by pancreaticoduodenectomy or pancreas-sparing duodenectomy. Some preliminary results have shown better outcomes with duodenectomy. A 45-year-old female with FAP had restorative proctocolectomy at 24 years, desmoid of the mesentery with regression after sulindac, two pregnancies, and at the age of 37 years had duodenal polyposis stage III carpeting the periampullary region. Endoscopic papillectomy and extensive piecemeal mucosectomy was performed but was unsuccessful due to recurrence. After 7 years of regular endoscopic surveillance, focal high-grade dysplasia was diagnosed at the last evaluation. Some diminutive polyps were seen in the small-bowel capsule endoscopy. MRCP showed a normal biliary and pancreatic duct without visualization of the Santorini duct. A pancreas and pylorus-preserving duodenectomy was performed with 3 main steps: (1) duodenectomy with preservation of the pancreas and the pylorus; (2) reconstruction with an advanced jejunal limb and duodenojejunostomy; (3) reimplantation of the biliary and pancreatic duct in the jejunal loop. The patient was discharged on the 11th postoperative day without complications. In conclusion, pancreas- and pylorus-preserving duodenectomy is a promising alternative to pancreaticoduodenectomy for advanced duodenal polyposis that allows complete endoscopic surveillance.
大多数家族性腺瘤性息肉病(FAP)患者会出现十二指肠息肉,其中5%会发展为癌症。处于斯皮格尔曼IV期的患者10年内患癌风险为36%。对于早期疾病,需要进行内镜监测并局部切除。无法切除的十二指肠疾病和严重发育异常是通过胰十二指肠切除术或保留胰腺的十二指肠切除术进行预防性根治性手术的指征。一些初步结果显示十二指肠切除术的效果更好。一名45岁的FAP女性在24岁时接受了保留直肠结肠切除术,肠系膜硬纤维瘤在舒林酸治疗后消退,经历了两次妊娠,37岁时十二指肠息肉病III期覆盖壶腹周围区域。进行了内镜乳头切除术和广泛的分片黏膜切除术,但因复发而未成功。经过7年的定期内镜监测,上次评估时诊断为局灶性高级别发育异常。小肠胶囊内镜检查发现一些微小息肉。磁共振胰胆管造影(MRCP)显示胆管和胰管正常,未显示副胰管。进行了保留胰腺和幽门的十二指肠切除术,主要有3个步骤:(1)保留胰腺和幽门进行十二指肠切除术;(2)用一段高位空肠进行重建并做十二指肠空肠吻合术;(3)将胆管和胰管重新植入空肠袢。患者术后第11天出院,无并发症。总之,对于晚期十二指肠息肉病,保留胰腺和幽门的十二指肠切除术是胰十二指肠切除术的一种有前景的替代方法,可实现完整的内镜监测。