Mao Weilin, Lyu Yang, Pu Ning, Li Jian'ang, Xin Baobao, Chen Wenqi, Jin Dayong, Lou Wenhui, Xu Xuefeng
Department of General Surgery, Zhongshan Hospital, Fudan University, Shanghai 200032, China.
Department of General Surgery,Jinshan Hospital, Fudan University, Shanghai 201508, China.
Zhonghua Wei Chang Wai Ke Za Zhi. 2018 May 25;21(5):564-568.
To investigate clinicopathological features and prognostic factors of appendiceal neuroendocrine neoplasms(a-NEN).
Clinical data of 20 patients diagnosed with a-NEN at Zhongshan Hospital of Fudan University between January 2000 and December 2016 were retrospectively analyzed. Pathological diagnosis was based on the WHO classification criteria of digestive system tumors (2010 edition). Based on the mitotic count and Ki-67 index, a-NENs were divided into grade 1 neuroendocrine tumor (NET G1), grade 2(G2) NET G2) and grade 3 (neuroendocrine carcinoma, NEC). Some special types of a-NEN (e.g. goblet cell carcinoid) and mixed adenoneuroendocrine neoplasms were classified as mixed adenoneuroendocrine carcinoma (MANEC). Follow-up was conducted by telephone or return visits. Univariate analysis was carried out using the Kaplan-Meier method, and the log-rank test was used to draw survival curves.
Of 20 patients, 14 were male and 6 were female with median age of 54 years. Seventeen cases presented acute right lower quadrant abdominal pain, 1 chronic right lower quadrant abdominal pain, 1 persistent abdominal discomfort with outburst whole abdominal pain and 1 was found during body check without symptoms. Twenty cases comprised 8 G1 patients, 4 G2 patients, 3 G3 patients, and 5 MANEC patients. When diagnosed, there was 1 patient with liver metastasis, 1 patient with abdominal and pelvic metastases, and 2 patients with postoperative pathological findings of lymph node metastasis. Six patients underwent appendectomy, 12 underwent right hemicolectomy, 1 underwent right hemicolectomy plus small intestine resection, and 1 underwent partial hepatectomy plus right hemicolectomy. The follow-up time was 7-187 months(average, 36 months). The total 1- and 3-year survival rates were 94.7% and 60.2%, respectively. Univariate analysis showed that age >50 years (χ=7.036, P=0.008), pathology grade as MANEC (χ=5.297, P=0.021), and metastasis (χ=6.558, P=0.010) indicated lower 5-year survival rate.
Most a-NEN patients have no typical symptoms, and the main complaint at consultation is acute right lower quadrant abdominal pain. Prognosis is poor for patients with age >50 years, MANEC pathology grade and metastasis.
探讨阑尾神经内分泌肿瘤(a-NEN)的临床病理特征及预后因素。
回顾性分析2000年1月至2016年12月在复旦大学附属中山医院确诊为a-NEN的20例患者的临床资料。病理诊断依据世界卫生组织消化系统肿瘤分类标准(2010年版)。根据核分裂象计数和Ki-67指数,将a-NEN分为1级神经内分泌肿瘤(NET G1)、2级(G2)NET G2)和3级(神经内分泌癌,NEC)。一些特殊类型的a-NEN(如杯状细胞类癌)和混合性腺神经内分泌肿瘤被归类为混合性腺神经内分泌癌(MANEC)。通过电话或复诊进行随访。采用Kaplan-Meier法进行单因素分析,并用log-rank检验绘制生存曲线。
20例患者中,男性14例,女性6例,中位年龄54岁。17例表现为急性右下腹疼痛,1例为慢性右下腹疼痛,1例为持续性腹部不适伴突发全腹痛,1例在体检时发现无症状。20例患者中包括8例G1患者、4例G2患者、3例G3患者和5例MANEC患者。确诊时,1例有肝转移,1例有腹部和盆腔转移,2例术后病理发现有淋巴结转移。6例行阑尾切除术,12例行右半结肠切除术,1例行右半结肠切除术加小肠切除术,1例行肝部分切除术加右半结肠切除术。随访时间为7 - 187个月(平均36个月)。1年和3年总生存率分别为94.7%和60.2%。单因素分析显示,年龄>50岁(χ=7.036,P = 0.008)、病理分级为MANEC(χ=5.297,P = 0.021)和有转移(χ=6.558,P = 0.010)提示5年生存率较低。
大多数a-NEN患者无典型症状,就诊时主要主诉为急性右下腹疼痛。年龄>50岁、病理分级为MANEC及有转移的患者预后较差。