Deveney C W, Deveney K E, Stark D, Moss A, Stein S, Way L W
Ann Surg. 1983 Oct;198(4):546-53. doi: 10.1097/00000658-198310000-00015.
Exploratory laparotomy and a search for gastrinomas was performed in 52 patients with the Zollinger-Ellison syndrome (ZES). Gastrinoma tissue was resected in 11 patients (21%), 6 (12%) of whom appear to have been cured. After surgery, serum gastrin levels in these six patients have remained normal from 10 months to 10 years. In the 46 other patients, tumor was unresectable because of metastases or multiple primary tumors (21 patients; 40%) or inability to find the tumor at laparotomy (21 patients; 40%). Multiple pancreatic islet cell adenomata were found in six of seven patients with multiple endocrine neoplasia (MEN), indicating that patients with this condition usually have diffuse involvement of the pancreas. The results of CT scans correlated with findings at laparotomy in 13 of 16 patients. The smallest tumor detected by CT scans was 1 cm in diameter. CT technology is more accurate in finding gastrinomas now than in the past and has a useful role in preoperative evaluation. The possibility of resection should be seriously considered in every patient with Zollinger-Ellison syndrome. Abdominal CT scans, transhepatic portal venous sampling, and laparotomy should be used to find the tumor and to determine whether it is resectable. Using presently available methods, it should be possible to cure about 25% of patients with gastrinomas who do not have MEN and over 70% of those without MEN who appear to have a solitary tumor. Total pancreatectomy may be necessary to cure some patients with MEN, but that operation is rarely justified. The morbidity and mortality of surgical attempts at curing this disease have become minimal; we have had no deaths or serious complications following such operations in over 10 yrs. Total gastrectomy and indefinite use of H2-receptor blocking agents are the therapeutic options for patients with unresectable gastrinomas. Because H2-receptor blocking agents fail to control acid secretion in many patients after several yrs of therapy, total gastrectomy is indicated in a large proportion of patients whose tumors cannot be resected. Total gastrectomy in patients with ZES is also safe using current techniques; our last death following this operation for ZES occurred 15 yrs ago.
对52例佐林格-埃利森综合征(ZES)患者进行了剖腹探查并寻找胃泌素瘤。11例患者(21%)切除了胃泌素瘤组织,其中6例(12%)似乎已治愈。术后,这6例患者的血清胃泌素水平在10个月至10年期间一直保持正常。在其他46例患者中,由于转移或多发原发性肿瘤(21例;40%)或剖腹探查时未能找到肿瘤(21例;40%),肿瘤无法切除。7例多发性内分泌腺瘤病(MEN)患者中有6例发现多发胰岛细胞瘤,表明患有这种疾病的患者通常胰腺有弥漫性受累。16例患者中有13例CT扫描结果与剖腹探查结果相符。CT扫描检测到的最小肿瘤直径为1厘米。现在CT技术在发现胃泌素瘤方面比过去更准确,在术前评估中具有重要作用。对于每例佐林格-埃利森综合征患者都应认真考虑切除的可能性。应使用腹部CT扫描、经肝门静脉采血和剖腹探查来寻找肿瘤并确定其是否可切除。使用目前可用的方法,对于没有MEN的胃泌素瘤患者,约25%有望治愈,对于没有MEN且似乎为孤立性肿瘤的患者,超过70%有望治愈。对于一些患有MEN的患者,可能需要进行全胰切除术来治愈,但这种手术很少有必要。治疗这种疾病的手术尝试的发病率和死亡率已降至最低;在过去10多年里,我们进行此类手术后没有出现死亡或严重并发症。对于无法切除胃泌素瘤的患者,全胃切除术和长期使用H2受体阻滞剂是治疗选择。由于在数年治疗后,许多患者使用H2受体阻滞剂无法控制胃酸分泌,因此很大一部分肿瘤无法切除的患者需要进行全胃切除术。使用当前技术,ZES患者的全胃切除术也是安全的;我们上一例因ZES进行该手术后死亡发生在15年前。