Department ofGI Surgery, Ghent University Hospital, Ghent, Belgium.
Department of Digestive Oncology, Ghent University Hospital, Ghent, Belgium.
Acta Chir Belg. 2021 Aug;121(4):225-234. doi: 10.1080/00015458.2021.1894734. Epub 2021 May 31.
Mucinous appendiceal tumors with or without the pseudomyxoma peritonei (PMP) syndrome are rare, but often present as an incidental finding. The confusing histology and lack of large prospective trials result in a considerable diagnostic and therapeutic challenge in these patients. We propose treatment algorithms in patients with incidentally found mucinous epithelial appendiceal tumors, with or without PMP, based on the currently available evidence. The therapeutic approach should take into account the histology and grade of the primary appendix tumor, as well as those of the associated peritoneal disease.
黏液性阑尾肿瘤伴或不伴腹膜假黏液瘤(PMP)综合征较为罕见,但常为偶然发现。由于其组织学表现复杂,且缺乏大型前瞻性临床试验,这些患者的诊断和治疗极具挑战性。我们根据现有证据,为偶然发现的黏液性上皮性阑尾肿瘤患者(伴或不伴 PMP)提出了治疗方案。治疗方法应考虑阑尾原发肿瘤的组织学和分级,以及相关腹膜疾病的组织学和分级。