Delcore R, Friesen S R
Department of Surgery, University of Kansas Medical Center, Kansas City 66160-7309, USA.
Curr Opin Gen Surg. 1994:69-76.
The surgical treatment of patients with the Zollinger-Ellison syndrome has undergone a dramatic evolution since the syndrome was originally described. It is now recognized that an aggressive surgical approach is mandatory because of the malignant potential of gastrinomas in both the sporadic and the familial forms of the syndrome. Although initially regarded as an incurable neoplasm, it is now known that complete surgical resection of gastrinomas can result in eugastrinemia even in the presence of lymph node metastases. It is now recognized that extrapancreatic gastrinomas are more common than pancreatic gastrinomas, and the most common location for an extrapancreatic gastrinoma is the duodenal wall. Major improvements in preoperative imaging and intraoperative localization techniques combined with an increased awareness of the anatomic distribution of gastrinomas have markedly increased the surgeon's ability to care for and cure patients with the Zollinger-Ellison syndrome.
自卓-艾综合征最初被描述以来,该综合征患者的外科治疗经历了巨大的演变。现在人们认识到,由于散发性和家族性卓-艾综合征中胃泌素瘤都具有恶性潜能,积极的手术方法是必不可少的。尽管胃泌素瘤最初被认为是一种无法治愈的肿瘤,但现在已知即使存在淋巴结转移,完全切除胃泌素瘤也可导致胃泌素血症正常。现在人们认识到,胰腺外胃泌素瘤比胰腺胃泌素瘤更常见,胰腺外胃泌素瘤最常见的位置是十二指肠壁。术前成像和术中定位技术的重大改进,以及对胃泌素瘤解剖分布认识的提高,显著增强了外科医生治疗和治愈卓-艾综合征患者的能力。