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胰腺导管扩张型黏液产生肿瘤——胰腺肿瘤形成的新概念

Duct-ectatic type of mucin producing tumor of the pancreas--new concept of pancreatic neoplasia.

作者信息

Kimura W, Sasahira N, Yoshikawa T, Muto T, Makuuchi M

机构信息

First Department of Surgery, Faculty of Medicine, University of Tokyo, Japan.

出版信息

Hepatogastroenterology. 1996 May-Jun;43(9):692-709.

PMID:8799417
Abstract

BACKGROUND/AIMS: Although there have been recent reports of mucin-producing tumor of the pancreas, there has been no thorough clinicopathological analysis of a large number of cases.

MATERIALS AND METHODS

Two hundred forty four cases of mucin-producing tumor of the pancreas from Japanese, European and American reports, together with 15 cases of our own, were analyzed clinicopathologically.

RESULTS

Mucin-producing tumor of the pancreas was found in 177 males and 82 females (M:F = 2.2:1). The mean age was 65.5 years. Jaundice, diabetes mellitus and a past history of pancreatitis were found in 15%-19% of the cases. The tumor was most frequently (62%) found in the head of the pancreas. Pathologically, hyperplasia or adenoma was found in 58 cases, and adenocarcinoma in 160 cases. Five-year-survival rate by the Kaplan-Meier method was 82.6% in all of the cases and postoperative survival curve was much better in cases with this type of carcinoma than in cases with ordinary pancreatic duct cell carcinoma (5-year-survival rate: 82.6% vs 17.3%). Serum tumor markers such as CEA or CA 19-9 were not effective in differentiating between benign and malignant, or in determining the degree of cancerous spread, while cytology of the pancreatic juice and biopsy of the tumor could contribute to the diagnosis.

CONCLUSIONS

Mucin-producing tumor has unique clinicopathological characteristics, such as the dilated main pancreatic duct or branches, dilatation of the orifice of the papilla of Vater, or good prognosis. Since a diagnosis for benign or malignant is very difficult in some cases, methods for distinguishing benign from malignant lesions or for determining cancerous spread, such as molecular biological techniques, should be established.

摘要

背景/目的:尽管近期有关于胰腺黏液产生性肿瘤的报道,但尚未对大量病例进行全面的临床病理分析。

材料与方法

对来自日本、欧洲和美国报道的244例胰腺黏液产生性肿瘤病例以及我们自己的15例病例进行临床病理分析。

结果

胰腺黏液产生性肿瘤患者中男性177例,女性82例(男∶女 = 2.2∶1)。平均年龄为65.5岁。15% - 19%的病例出现黄疸、糖尿病和胰腺炎病史。肿瘤最常(62%)位于胰头。病理上,58例为增生或腺瘤,160例为腺癌。采用Kaplan - Meier法计算的所有病例5年生存率为82.6%,此类癌患者的术后生存曲线比普通胰腺导管细胞癌患者的要好得多(5年生存率:82.6%对17.3%)。血清肿瘤标志物如癌胚抗原(CEA)或糖类抗原19 - 9(CA 19 - 9)在区分良恶性或确定癌症扩散程度方面无效,而胰液细胞学检查和肿瘤活检有助于诊断。

结论

胰腺黏液产生性肿瘤具有独特的临床病理特征,如主胰管或分支扩张、 Vater壶腹开口扩张或预后良好。由于在某些病例中很难诊断良恶性,因此应建立如分子生物学技术等区分良性与恶性病变或确定癌症扩散的方法。

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