Department of Medicine, Hospital of the University of Pennsylvania, Perelman School of Medicine at the University of Pennsylvania, Philadelphia, Pennsylvania 19104, USA.
Clin Gastroenterol Hepatol. 2012 Nov;10(11):1262-9. doi: 10.1016/j.cgh.2012.08.014. Epub 2012 Aug 17.
BACKGROUND & AIMS: Zollinger-Ellison syndrome (ZES) is a rare disorder characterized by gastrin-secreting tumors of the gastrointestinal tract and gastric acid hypersecretion. There is controversy over the best way to manage these patients; we investigated outcomes of patients with different forms of the disease, who did and did not undergo surgery.
We performed a retrospective chart review of patients with ZES associated with multiple endocrine neoplasia type 1 (MEN-1) (n = 16) and those with sporadic ZES (n = 33) seen at a tertiary care center from August 1994 to January 2012. Cox proportional hazards modeling was used to compare survival times among groups, based on treatment with surgery (n = 34) and the presence of MEN-1 (n = 9 with surgery; n = 7 without surgery). Differences were compared using the unpaired Student t test and the Fisher exact test.
Patients with MEN-1 syndrome-associated ZES presented at a younger age than patients with sporadic ZES (34.9 vs 45.7 y, respectively; P < .05) and were diagnosed at a younger age (39.3 vs 49.7 y, respectively; P < .01), yet lived a similar number of years (55.9 vs 55.1 y, respectively; P = .91). None of the patients with MEN-1-associated ZES died of progressive disease, compared with 86% of deaths among patients with sporadic ZES (P < .05). Lymph node involvement, detected during surgery, increased the risk of metastasis to liver (P = .13) and lack of cure by surgery (P = .01). Surgery reduced all-cause mortality (hazard ratio, 0.11; 95% confidence interval, 0.2-0.6; P = .011) and disease-related mortality (hazard ratio, 0.14; 95% confidence interval, 0.2-0.84; P = .032) of patients with sporadic, but not MEN-1 syndrome-associated, ZES.
The presence of MEN-1 is associated with earlier onset and diagnosis of ZES, but a benign clinical course that rarely results in disease-related death; surgery therefore can be deferred for these patients. However, 86% of deaths among patients with sporadic ZES are attributed to disease-related causes, and mortality is reduced by early surgical intervention. Patients with sporadic ZES should undergo surgery soon after diagnosis.
卓-艾综合征(ZES)是一种罕见的疾病,其特征为胃肠道分泌胃泌素的肿瘤和胃酸分泌过多。对于此类患者的最佳治疗方式仍存在争议,我们对不同形式的 ZES 患者(接受或未接受手术治疗)的结局进行了研究。
我们对 1994 年 8 月至 2012 年 1 月在一家三级护理中心就诊的多发性内分泌肿瘤 1 型(MEN-1)相关 ZES 患者(n = 16)和散发性 ZES 患者(n = 33)进行了回顾性图表审查。基于手术治疗(n = 34)和 MEN-1 状态(n = 9 例手术治疗;n = 7 例未手术治疗),采用 Cox 比例风险模型比较各组的生存时间。采用未配对学生 t 检验和 Fisher 确切概率法比较差异。
MEN-1 综合征相关 ZES 患者的发病年龄较散发性 ZES 患者年轻(分别为 34.9 岁和 45.7 岁;P <.05),诊断年龄也较小(分别为 39.3 岁和 49.7 岁;P <.01),但生存年限相似(分别为 55.9 岁和 55.1 岁;P =.91)。与散发性 ZES 患者中 86%的死亡原因是疾病进展相比,无 1 例 MEN-1 相关 ZES 患者死于进行性疾病(P <.05)。手术中发现的淋巴结受累增加了肝脏转移的风险(P =.13)和手术无法治愈的风险(P =.01)。手术降低了散发性 ZES 患者的全因死亡率(风险比,0.11;95%置信区间,0.2-0.6;P =.011)和疾病相关死亡率(风险比,0.14;95%置信区间,0.2-0.84;P =.032)。
MEN-1 的存在与 ZES 的发病年龄和诊断年龄较早相关,但疾病过程通常良性,很少导致疾病相关死亡;因此,此类患者可以延迟手术。然而,散发性 ZES 患者中 86%的死亡归因于疾病相关原因,早期手术干预可降低死亡率。散发性 ZES 患者应在确诊后尽快接受手术。