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佐林格-埃利森综合征的手术改变了胃泌素瘤的自然病程。

Surgery in Zollinger-Ellison syndrome alters the natural history of gastrinoma.

作者信息

Fraker D L, Norton J A, Alexander H R, Venzon D J, Jensen R T

机构信息

Surgical Metabolism Section, National Cancer Institute, National Institutes of Health, Bethesda, Maryland.

出版信息

Ann Surg. 1994 Sep;220(3):320-8; discussion 328-30. doi: 10.1097/00000658-199409000-00008.

Abstract

OBJECTIVE

The authors assessed the impact of gastrinoma resection on the subsequent development of hepatic metastases in Zollinger-Ellison syndrome.

SUMMARY BACKGROUND DATA

The symptoms of acid hypersecretion can be controlled medically in Zollinger-Ellison syndrome with high-dose pharmacologic therapy. The current role of surgery is curative excision of the gastrinoma. Because biochemical cure is obtained only in a portion of the patients and the neoplastic disease may be indolent in this syndrome, the ability of surgical resection of gastrinoma to alter or improve the subsequent development of hepatic metastases and mortality has not been defined.

METHODS

One hundred twenty-four patients with the biochemical diagnosis of Zollinger-Ellison syndrome and no hepatic metastases on initial imaging studies were evaluated. Ninety-eight patients underwent surgical exploration for curative gastrinoma resections while 26 patients were managed medically. Long-term follow-up regarding development of hepatic metastases and survival were evaluated.

RESULTS

Surgical exploration with gastrinoma excision resulted in a significantly decreased incidence of hepatic metastases 3% (3/98) compared with patients managed medically 23% (6/26) with comparable follow-up (p < 0.003). Two deaths due to metastatic gastrinoma occurred in the nonoperative group compared with no disease-specific deaths in the surgical group (p = 0.085).

CONCLUSIONS

For the patient with Zollinger-Ellison syndrome without metastatic disease, surgical exploration with attempted curative gastrinoma resection is recommended because it may alter the natural history of this syndrome.

摘要

目的

作者评估胃泌素瘤切除术对卓艾综合征肝转移后续发展的影响。

总结背景数据

卓艾综合征中胃酸分泌过多的症状可通过大剂量药物治疗进行医学控制。目前手术的作用是根治性切除胃泌素瘤。由于仅部分患者可实现生化治愈,且该综合征中的肿瘤性疾病可能进展缓慢,胃泌素瘤手术切除改变或改善肝转移后续发展及死亡率的能力尚未明确。

方法

对124例经生化诊断为卓艾综合征且初始影像学检查无肝转移的患者进行评估。98例患者接受了旨在根治性切除胃泌素瘤的手术探查,而26例患者接受药物治疗。评估肝转移发生情况及生存的长期随访结果。

结果

与接受药物治疗的患者相比,接受胃泌素瘤切除的手术探查使肝转移发生率显著降低,在可比随访期内分别为3%(3/98)和23%(6/26)(p < 0.003)。非手术组有2例因转移性胃泌素瘤死亡,而手术组无疾病特异性死亡(p = 0.085)。

结论

对于无转移性疾病的卓艾综合征患者,建议进行旨在根治性切除胃泌素瘤的手术探查,因为这可能改变该综合征的自然病程。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/12f9/1234386/9e4a4fdadd2f/annsurg00055-0112-a.jpg

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