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World J Surg Oncol. 2018 Jul 14;16(1):142. doi: 10.1186/s12957-018-1446-y.
4
Somatostatinoma Masquerading as Chronic Pancreatitis.伪装成慢性胰腺炎的生长抑素瘤
Pancreas. 2018 Apr;47(4):e19-e20. doi: 10.1097/MPA.0000000000001011.
5
Trends in the Incidence, Prevalence, and Survival Outcomes in Patients With Neuroendocrine Tumors in the United States.美国神经内分泌肿瘤患者的发病率、患病率和生存结局趋势。
JAMA Oncol. 2017 Oct 1;3(10):1335-1342. doi: 10.1001/jamaoncol.2017.0589.
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Pancreatic neuroendocrine tumors: contemporary diagnosis and management.胰腺神经内分泌肿瘤:当代诊断与管理
Hosp Pract (1995). 2016 Aug;44(3):109-19. doi: 10.1080/21548331.2016.1210474. Epub 2016 Jul 18.
7
Clinical Presentation and Diagnosis of Pancreatic Neuroendocrine Tumors.胰腺神经内分泌肿瘤的临床表现与诊断
Surg Oncol Clin N Am. 2016 Apr;25(2):363-74. doi: 10.1016/j.soc.2015.12.003. Epub 2016 Feb 18.
8
Placebo-Controlled, Double-Blind, Prospective, Randomized Study on the Effect of Octreotide LAR in the Control of Tumor Growth in Patients with Metastatic Neuroendocrine Midgut Tumors (PROMID): Results of Long-Term Survival.奥曲肽长效注射剂(LAR)对转移性中肠神经内分泌肿瘤患者肿瘤生长控制效果的安慰剂对照、双盲、前瞻性、随机研究(PROMID):长期生存结果
Neuroendocrinology. 2017;104(1):26-32. doi: 10.1159/000443612. Epub 2016 Jan 6.
9
Lanreotide in metastatic enteropancreatic neuroendocrine tumors.兰瑞肽治疗转移性胃肠胰神经内分泌肿瘤。
N Engl J Med. 2014 Jul 17;371(3):224-33. doi: 10.1056/NEJMoa1316158.
10
Pancreatic somatostatinoma diagnosed preoperatively: report of a case.术前诊断的胰腺生长抑素瘤:病例报告
JOP. 2014 Jan 10;15(1):66-71. doi: 10.6092/1590-8577/1884.

胰腺生长抑素瘤的临床病理数据和治疗方式。

Clinicopathological Data and Treatment Modalities for Pancreatic Somatostatinomas.

机构信息

First Department of Surgery, National and Kapodistrian University of Athens, Laikon General Hospital, Athens, Greece

First Department of Surgery, National and Kapodistrian University of Athens, Laikon General Hospital, Athens, Greece.

出版信息

In Vivo. 2020 Nov-Dec;34(6):3573-3582. doi: 10.21873/invivo.12201.

DOI:10.21873/invivo.12201
PMID:33144470
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7811659/
Abstract

BACKGROUND/AIM: Somatostatinomas (SSomas) constitute a rare neuroendocrine tumor. The purpose of this study was to evaluate the current published literature about pancreatic SSomas and report epidemiologic and clinicopathologic data for this entity.

PATIENTS AND METHODS

A combined automated and manual systematic database search of the literature was performed using electronic search engines (Medline PubMed, Scopus, Ovid and Cochrane Library), until February 2020. Statistical analysis was performed using the R language and environment for statistical computing.

RESULTS

Overall, the research revealed a total of 36 pancreatic SSoma cases. Patient mean age was 50.25 years. The most common pancreatic location was the pancreatic head (61.8%). The most frequent clinical symptom was abdominal pain (61.1%). Diagnostic algorithm most often included Computed Tomography and biopsy; surgical resection was performed in 28 cases. Out of the 36 cases, 22 had been diagnosed with a metastatic tumor and metastasectomy was performed in 6 patients with a worse overall survival (OS) (p=0.029). In total, OS was 47.74 months.

CONCLUSION

Patients with metastatic disease did not benefit from metastasectomy, but the sample size was small to reach definite conclusions. However, further studies with longer follow-up are needed for a better evaluation of these results.

摘要

背景/目的:生长抑素瘤(SSomas)是一种罕见的神经内分泌肿瘤。本研究旨在评估目前关于胰腺 SSoma 的文献,并报告该实体的流行病学和临床病理数据。

患者和方法

使用电子搜索引擎(Medline PubMed、Scopus、Ovid 和 Cochrane Library)对文献进行了联合自动化和手动系统数据库搜索,检索时间截至 2020 年 2 月。使用 R 语言和环境进行统计分析。

结果

总体而言,研究共发现 36 例胰腺 SSoma 病例。患者平均年龄为 50.25 岁。最常见的胰腺位置是胰头部(61.8%)。最常见的临床症状是腹痛(61.1%)。最常用的诊断算法包括计算机断层扫描和活检;28 例患者进行了手术切除。在 36 例病例中,有 22 例被诊断为转移性肿瘤,6 例患者进行了转移性肿瘤切除术,总生存期(OS)更差(p=0.029)。总体而言,OS 为 47.74 个月。

结论

患有转移性疾病的患者不能从转移瘤切除术获益,但样本量较小,无法得出明确结论。然而,为了更好地评估这些结果,需要进行随访时间更长的进一步研究。