Nozari Neda, Nikfam Sepideh, Nikmanesh Arash, Mohammadnejad Mehdi, Sotoudehmanesh Rasoul, Zamani Farhad, Merat Shahin, Malekzadeh Reza, Pourshams Akram
Liver and Pancreatobiliary Diseases Research Center, Digestive Diseases Research Institute, Tehran University of Medical Sciences, Tehran, Iran.
Department of Pathology, Masood Clinic, Tehran, Iran.
Middle East J Dig Dis. 2014 Jul;6(3):151-5.
BACKGROUND Pancreatic neuroendocrine tumors (PNETs) are rare tumors with variable malignant potential, prognosis, and survival. We aimed to assess the characteristics of patients with non- functional PNET in our hospital. METHODS From Nov 2010 to Nov 2013 , all patients who came to endosonography unit of Shariati hospital , Tehran , Iran , and had pancreatic lesions were assessed . Tumor samples were obtained through fine needle aspiration. Various characteristics of the non- functional PNET were recorded and patients were followed up to three years. RESULTS Twenty eight non func-PNET cases, aged 37-72 years were identified, 15 (53.6%) of whom were men. Fifteen (53.6%) tumors were located in the head and 5(17.8%) in the body of the pancreas. The mean tumor size was 3.9 Cm and 10.7% , 28.6%, 32.1%, and 28.6% of the patients were at stages I, II, III and IV, respectively. Of the patients, 12 (43%) underwent surgery, 3 (10.7%) received chemotherapy, and 13 (46.4%) received no treatment. During the mean follow-up of 16 months, the disease had progressed in 3 (10.7%) patients and 10 (35.7%) had died. In univariate analysis, tumor size>3Cm and Ki-67>20% were correlated with survival rate but not in multivariate analysis. CONCLUSION Iranian patients with non- functional PNET present similar characteristics to world patients. There is a need to establish efficacy of tumor samples which are obtaining through fine needle aspiration for assessing tumor grading.
胰腺神经内分泌肿瘤(PNETs)是一种罕见肿瘤,其恶性潜能、预后和生存率各不相同。我们旨在评估我院非功能性PNET患者的特征。方法:2010年11月至2013年11月,对所有前往伊朗德黑兰沙里亚蒂医院内镜超声科且有胰腺病变的患者进行评估。通过细针穿刺获取肿瘤样本。记录非功能性PNET的各种特征,并对患者进行长达三年的随访。结果:共识别出28例非功能性PNET病例,年龄在37至72岁之间,其中15例(53.6%)为男性。15例(53.6%)肿瘤位于胰头,5例(17.8%)位于胰体。肿瘤平均大小为3.9厘米,分别有10.7%、28.6%、32.1%和28.6%的患者处于I、II、III和IV期。患者中,12例(43%)接受了手术,3例(10.7%)接受了化疗,13例(46.4%)未接受治疗。在平均16个月的随访期间,3例(10.7%)患者病情进展,10例(35.7%)死亡。单因素分析中,肿瘤大小>3厘米和Ki-67>20%与生存率相关,但多因素分析中并非如此。结论:伊朗非功能性PNET患者的特征与世界其他患者相似。有必要确定通过细针穿刺获取的肿瘤样本在评估肿瘤分级方面的有效性。