Suppr超能文献

空肠和回肠类癌:167例的免疫组织化学及临床病理研究

Carcinoids of the jejunum and ileum: an immunohistochemical and clinicopathologic study of 167 cases.

作者信息

Burke A P, Thomas R M, Elsayed A M, Sobin L H

机构信息

Department of Hepatic and Gastrointestinal Pathology, Armed Forces Institute of Pathology, Washington, DC 20306-6000, USA.

出版信息

Cancer. 1997 Mar 15;79(6):1086-93.

PMID:9070484
Abstract

BACKGROUND

Carcinoid tumors of the gastrointestinal tract differ in their clinical and histopathologic features, depending on the site of origin. There are few clinicopathologic studies that specifically describe jejunoileal carcinoid tumors.

METHODS

One hundred sixty-seven ileal and jejunal carcinoids were retrospectively studied with emphasis on clinical, pathologic, immunohistochemical, and prognostic features.

RESULTS

The mean age of patients at the time of presentation was 62 +/- 12 years (range, 13-93 years). Eight patients had carcinoid syndrome (5%) and 1 had Zollinger-Ellison syndrome. Twenty-six percent of tumors were multiple, and 77% were transmurally invasive; 31% had regional lymph node metastases only, and 32% had liver or mesenteric metastases. Ninety-three percent of tumors had an insular growth pattern. Serotonin was expressed in 86% of tumors (86 of 102), chromogranin in 92%, and neuron specific enolase in 95%. Twenty percent of tumors (10 of 51) expressed prostatic acid phosphatase; 96% were argyrophil, and 98% argentaffin. Of 80 cases with follow-up data (mean follow-up, 52 +/- 5 months), 21% were dead of disease, 16% were dead of other causes, 19% were alive with disease, and 44% had no evidence of disease at last follow-up. The 5-year Kaplan-Meier survival estimate for all cases was 58%. By univariate analysis, survival was negatively correlated with distant metastases at the time of surgery (P = 0.002), mitotic rate (P = 0.01), tumor multiplicity (P = 0.01), the presence of carcinoid syndrome (P = 0.02), depth of invasion (P = 0.03), and female gender (P = 0.05); by multivariate analysis, survival was negatively associated with distant metastasis (P = 0.002), carcinoid syndrome (P = 0.01), and female gender (P = 0.03).

CONCLUSIONS

Jejunoileal carcinoid tumors have a relatively high rate of transmural invasion and aggressive clinical behavior. They are usually insular and largely argentaffin, with a high rate of chromogranin and serotonin positivity. These features differentiate jejunoileal carcinoids from other gastrointestinal carcinoids.

摘要

背景

胃肠道类癌肿瘤的临床和组织病理学特征因其起源部位而异。很少有临床病理学研究专门描述空肠回肠类癌肿瘤。

方法

对167例回肠和空肠类癌进行回顾性研究,重点关注临床、病理、免疫组化和预后特征。

结果

患者就诊时的平均年龄为62±12岁(范围13 - 93岁)。8例患者有类癌综合征(5%),1例有佐林格-埃利森综合征。26%的肿瘤为多发,77%为透壁浸润;31%仅有区域淋巴结转移,32%有肝或肠系膜转移。93%的肿瘤呈岛状生长模式。86%的肿瘤(102例中的86例)表达血清素,92%表达嗜铬粒蛋白,95%表达神经元特异性烯醇化酶。20%的肿瘤(51例中的10例)表达前列腺酸性磷酸酶;96%为嗜银性,98%为亲银性。在80例有随访数据的病例中(平均随访时间52±5个月),21%死于疾病,16%死于其他原因,19%带瘤生存,44%在最后一次随访时无疾病证据。所有病例的5年Kaplan-Meier生存估计为58%。单因素分析显示,生存与手术时的远处转移(P = 0.002)、有丝分裂率(P = 0.01)、肿瘤多发性(P = 0.01)、类癌综合征的存在(P = 0.02)、浸润深度(P = 0.03)以及女性性别(P = 0.05)呈负相关;多因素分析显示,生存与远处转移(P = 0.002)、类癌综合征(P = 0.01)以及女性性别(P = 0.03)呈负相关。

结论

空肠回肠类癌肿瘤透壁浸润率相对较高,临床行为具有侵袭性。它们通常呈岛状,大多为亲银性,嗜铬粒蛋白和血清素阳性率较高。这些特征将空肠回肠类癌与其他胃肠道类癌区分开来。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验