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监测对散发性 Zollinger-Ellison 综合征患者多发性内分泌肿瘤-1 和手术的重要性。

Importance of surveillance for multiple endocrine neoplasia-1 and surgery in patients with sporadic Zollinger-Ellison syndrome.

机构信息

Department of Medicine, Hospital of the University of Pennsylvania, Perelman School of Medicine at the University of Pennsylvania, Philadelphia, Pennsylvania 19104, USA.

出版信息

Clin Gastroenterol Hepatol. 2012 Nov;10(11):1262-9. doi: 10.1016/j.cgh.2012.08.014. Epub 2012 Aug 17.

Abstract

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.

METHODS

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.

RESULTS

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.

CONCLUSIONS

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.

摘要

背景与目的

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。

方法

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。

结果

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)。

结论

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。

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