Zogakis Theresa G, Gibril Fathia, Libutti Steven K, Norton Jeffrey A, White Donald E, Jensen Robert T, Alexander H Richard
Surgery Branch, Center for Cancer Research, National Cancer Institute/National Institutes of Health, Building 10, Room 2B07, 10 Center Drive, Bethesda, MD 20892-1502, USA.
Ann Surg. 2003 Jul;238(1):42-8. doi: 10.1097/01.SLA.0000074963.87688.31.
Primary duodenal gastrinomas are now recognized as a common etiology for patients with sporadic Zollinger Ellison Syndrome (ZES); however, the clinical and pathologic features of this condition and long-term outcome after operation are not well characterized.
Between November 1982 and September 2000, 63 patients diagnosed with sporadic ZES underwent resection of a primary duodenal gastrinoma and regional nodal metastases with curative intent. Data from a prospectively maintained database were reviewed for clinical and pathologic parameters relating to primary tumor size, location, frequency of lymph node metastases, and disease-specific and disease-free survival.
There were 41 males and 22 females (mean age, 48.6 years). The majority of duodenal gastrinomas were in the first or second portions of the duodenum (83%). Tumor size ranged from 0.2 to 2.0 cm with 62% measuring less than 1.0 cm. Sixty percent of individuals had regional lymph node metastases identified primarily in proximity to the primary tumor. At a median 10-year follow-up, the overall disease-specific and disease-free survivals were 100% and 60%, respectively. Actuarial 10-year disease-free survival was significantly higher for patients without lymph node metastases versus those with lymph node metastases (78% versus 48%, P = 0.0137).
Duodenal gastrinomas in patients with sporadic ZES are frequently small, most commonly located in the proximal duodenum, and associated with regional lymph node metastases in 60%. Disease-free survival is lower for patients with regional lymph node metastases suggesting that a more systematic lymphadenectomy to extirpate occult disease may be indicated in this group.
原发性十二指肠胃泌素瘤现已被认为是散发性佐林格-埃利森综合征(ZES)患者的常见病因;然而,这种疾病的临床和病理特征以及手术后的长期预后尚未得到充分描述。
在1982年11月至2000年9月期间,63例被诊断为散发性ZES的患者接受了原发性十二指肠胃泌素瘤及区域淋巴结转移灶的切除,目的是治愈疾病。回顾了来自前瞻性维护数据库的数据,以获取与原发性肿瘤大小、位置、淋巴结转移频率以及疾病特异性生存率和无病生存率相关的临床和病理参数。
男性41例,女性22例(平均年龄48.6岁)。大多数十二指肠胃泌素瘤位于十二指肠的第一或第二部分(83%)。肿瘤大小从0.2厘米至2.0厘米不等,62%的肿瘤直径小于1.0厘米。60%的患者有区域淋巴结转移,主要位于原发性肿瘤附近。在中位10年的随访中,总体疾病特异性生存率和无病生存率分别为100%和60%。无淋巴结转移患者的精算10年无病生存率显著高于有淋巴结转移的患者(78%对48%,P = 0.0137)。
散发性ZES患者的十二指肠胃泌素瘤通常较小,最常见于十二指肠近端,60%与区域淋巴结转移相关。有区域淋巴结转移的患者无病生存率较低,这表明对于该组患者可能需要进行更系统的淋巴结清扫以清除隐匿性疾病。