Gao Wei, Liu Shang-mei, Lu Hai-zhen, Liang Jing, Yuan Yan-ling, Liu Xiu-yun
Department of Pathology, Cancer Institute (Hospital), Chinese Academy of Medical Science and Peking Union Medical College, Beijing 100021, China.
Zhonghua Zhong Liu Za Zhi. 2012 Jun;34(6):450-6. doi: 10. 3760/cma.j.issn.0253-3766.2012.06.011.
To analyze the clinicopathological features of intestinal neuroendocrine neoplasms.
The clinicopathological features of 114 patients with intestinal neuroendocrine neoplasms treated in our hospital from April 1999 to March 2011 were retrospectively reviewed, including tumor location, histological classification, muscle invasion, metastasis and clinical data. Immunohistochemical SP staining was applied to examine the expression of 15 markers in the tumor specimens.
The male:female ratio of the patients was 1.33, and most of the tumors were located in the rectum of polypoid type. The positive rate of immunohistochemical staining of Syn expression was 97.4%, NSE 95.6%, PGP9.5 84.2%, CD56 75.4%, CD57 72.8%, CgA 43.0%, S100 36.0%, Syn combined with CgA 99.1%, and the two marker Syn and CgA combined with any one of CD56, CD57 or PGP9.5 reached to 100%. The 5-years survival rates of G1, G2 were 98.9% and 76.9%, respectively, and the overall 5-year survival rate of intestinal neuroendocrine neoplasms was 92.9%. Two of the 7 cases of poor differentiated neuroendocrine carcinoma died after operation, another 2 of them lost to follow up. Others were still alive during the follow-up. Among the 3 patients with small cell carcinoma, two survived for 8 to 24 months after operation, and one lost to follow up. Two cases of mixed adenoneuroendocrine carcinoma (MANEC) were still surviving during the follow-up. Different histological types of intestinal neuroendocrine neoplasms were significantly different in sex, primary tumor site, pathological type, tumor size, types of combined tumors, pT stage, aggressive nervous and vascular invasion, and metastasis (all P < 0.05). Single factor analysis of the intestinal neuroendocrine neoplasms indicated that tumor size (Z = -6.334, P < 0.001), histological classification (χ(2) = 31.175, P < 0.001) and muscle invasion (χ(2) = 63.567, P < 0.001) were associated with metastasis of intestinal neuroendocrine neoplasms. Logistic analysis showed that muscle invasion was the main behavior risk factor of this tumor (OR = 1.827, P < 0.05).
Intestinal neuroendocrine neoplasms usually occur in males, and the most common involved organ is the rectum. Their histological types are related to the prognosis, and the depth of invasion is an important metastasis factor of intestinal neuroendocrine neoplasms. Of the neuroendocrine makers, the combination of CgA and Syn shows a higher diagnostic sensitivity.
分析肠道神经内分泌肿瘤的临床病理特征。
回顾性分析1999年4月至2011年3月在我院接受治疗的114例肠道神经内分泌肿瘤患者的临床病理特征,包括肿瘤部位、组织学分类、肌层浸润、转移情况及临床资料。采用免疫组织化学SP法检测肿瘤标本中15种标志物的表达。
患者男女比例为1.33,多数肿瘤位于直肠,呈息肉样。免疫组织化学染色中,Syn表达阳性率为97.4%,NSE为95.6%,PGP9.5为84.2%,CD56为75.4%,CD57为72.8%,CgA为43.0%,S100为36.0%,Syn联合CgA为99.1%,Syn与CgA联合CD56、CD57或PGP9.5中任一项的阳性率达100%。G1、G2级的5年生存率分别为98.9%和76.9%,肠道神经内分泌肿瘤总体5年生存率为92.9%。7例低分化神经内分泌癌中,2例术后死亡,另2例失访,其余随访期间仍存活。3例小细胞癌患者中,2例术后存活8至24个月,1例失访。2例混合性腺神经内分泌癌(MANEC)随访期间仍存活。不同组织学类型的肠道神经内分泌肿瘤在性别、原发肿瘤部位、病理类型、肿瘤大小、合并肿瘤类型、pT分期、神经和血管侵犯情况及转移方面差异均有统计学意义(均P < 0.05)。肠道神经内分泌肿瘤的单因素分析表明,肿瘤大小(Z = -6.334,P < 0.001)、组织学分类(χ(2) = 31.175,P < 0.001)及肌层浸润(χ(2) = 63.567,P < 0.001)与肠道神经内分泌肿瘤转移有关。Logistic分析显示,肌层浸润是该肿瘤主要的行为危险因素(OR = 1.827,P < 0.05)。
肠道神经内分泌肿瘤好发于男性,最常累及的器官是直肠。其组织学类型与预后相关,浸润深度是肠道神经内分泌肿瘤重要的转移因素。在神经内分泌标志物中,CgA与Syn联合显示出较高的诊断敏感性。