胰腺透明细胞癌:一种异常表型的腺癌,起源于导管细胞。

Atsushi Sasaki, Tetsuya Ishio, Toshio Bandoh, Kohei Shibata, Toshifumi Matsumoto, Masanori Aramaki, Katsunori Kawano, Seigo Kitano, Kenji Kashima, Shigeo Yokoyama
{"title":"胰腺透明细胞癌:一种异常表型的腺癌,起源于导管细胞。","authors":"Atsushi Sasaki,&nbsp;Tetsuya Ishio,&nbsp;Toshio Bandoh,&nbsp;Kohei Shibata,&nbsp;Toshifumi Matsumoto,&nbsp;Masanori Aramaki,&nbsp;Katsunori Kawano,&nbsp;Seigo Kitano,&nbsp;Kenji Kashima,&nbsp;Shigeo Yokoyama","doi":"10.1007/s00534-003-0843-x","DOIUrl":null,"url":null,"abstract":"<p><p>Although clear cell carcinoma has been found in various organs, only six cases have been reported in the pancreas. Moreover, the histogenesis of clear cell carcinoma of the pancreas remains controversial. We report a case of clear cell carcinoma of the pancreas in a 61-year-old woman, with an unusual pheno- or genotype detected by histochemical, immunohistochemical, and K- ras oncogene analyses. Histologically, the pancreatic tumor was predominantly composed of clear cell nests with scanty fibrous stroma and scattered duct-like structures. Neither clear cell nor duct-like components of the tumor showed mucin production. Immunohistochemical analysis of neoplastic cells showed a positive reaction to antibodies against cytokeratins 8 and 19, carbohydrate antigen 19-9, and alpha-1-antitrypsin, and showed no reaction to antibodies against carcinoembryonic antigen, neuroendocrine markers, trypsin, amylase, and HMB45. K- ras analysis revealed no mutation at codon 12 in either clear cell or duct-like components. The patient has had no recurrence as yet. The pancreatic carcinoma in our patient may be of duct cell origin, but the results of histochemical, immunohistochemical, and gene analyses and patient's outcome were unusual compared with those of previous cases.</p>","PeriodicalId":15992,"journal":{"name":"Journal of hepato-biliary-pancreatic surgery","volume":"11 2","pages":"140-4"},"PeriodicalIF":0.0000,"publicationDate":"2004-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1007/s00534-003-0843-x","citationCount":"13","resultStr":"{\"title\":\"Clear cell carcinoma of the pancreas: an adenocarcinoma with unusual phenotype of duct cell origin.\",\"authors\":\"Atsushi Sasaki,&nbsp;Tetsuya Ishio,&nbsp;Toshio Bandoh,&nbsp;Kohei Shibata,&nbsp;Toshifumi Matsumoto,&nbsp;Masanori Aramaki,&nbsp;Katsunori Kawano,&nbsp;Seigo Kitano,&nbsp;Kenji Kashima,&nbsp;Shigeo Yokoyama\",\"doi\":\"10.1007/s00534-003-0843-x\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p>Although clear cell carcinoma has been found in various organs, only six cases have been reported in the pancreas. Moreover, the histogenesis of clear cell carcinoma of the pancreas remains controversial. We report a case of clear cell carcinoma of the pancreas in a 61-year-old woman, with an unusual pheno- or genotype detected by histochemical, immunohistochemical, and K- ras oncogene analyses. Histologically, the pancreatic tumor was predominantly composed of clear cell nests with scanty fibrous stroma and scattered duct-like structures. Neither clear cell nor duct-like components of the tumor showed mucin production. Immunohistochemical analysis of neoplastic cells showed a positive reaction to antibodies against cytokeratins 8 and 19, carbohydrate antigen 19-9, and alpha-1-antitrypsin, and showed no reaction to antibodies against carcinoembryonic antigen, neuroendocrine markers, trypsin, amylase, and HMB45. K- ras analysis revealed no mutation at codon 12 in either clear cell or duct-like components. The patient has had no recurrence as yet. The pancreatic carcinoma in our patient may be of duct cell origin, but the results of histochemical, immunohistochemical, and gene analyses and patient's outcome were unusual compared with those of previous cases.</p>\",\"PeriodicalId\":15992,\"journal\":{\"name\":\"Journal of hepato-biliary-pancreatic surgery\",\"volume\":\"11 2\",\"pages\":\"140-4\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2004-01-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://sci-hub-pdf.com/10.1007/s00534-003-0843-x\",\"citationCount\":\"13\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Journal of hepato-biliary-pancreatic surgery\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.1007/s00534-003-0843-x\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of hepato-biliary-pancreatic surgery","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1007/s00534-003-0843-x","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 13

摘要

虽然透明细胞癌已在各种器官中发现,但在胰腺中仅报道了6例。此外,胰腺透明细胞癌的组织发生仍有争议。我们报告一例61岁女性胰腺透明细胞癌,通过组织化学、免疫组织化学和K- ras癌基因分析检测出异常的表型或基因型。组织学上,胰腺肿瘤主要由透明的细胞巢、稀少的纤维间质和分散的导管样结构组成。肿瘤的透明细胞和导管样成分均未显示粘蛋白的产生。肿瘤细胞免疫组化分析显示对细胞角蛋白8和19、碳水化合物抗原19-9和α -1抗胰蛋白酶抗体呈阳性反应,对癌胚抗原、神经内分泌标志物、胰蛋白酶、淀粉酶和HMB45抗体无反应。K- ras分析显示,在透明细胞和导管样成分中,密码子12均未发生突变。这个病人到目前为止还没有复发。本例患者的胰腺癌可能是源自导管细胞,但其组织化学、免疫组织化学和基因分析结果及患者预后与以往病例相比都不寻常。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
查看原文
分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
Clear cell carcinoma of the pancreas: an adenocarcinoma with unusual phenotype of duct cell origin.

Although clear cell carcinoma has been found in various organs, only six cases have been reported in the pancreas. Moreover, the histogenesis of clear cell carcinoma of the pancreas remains controversial. We report a case of clear cell carcinoma of the pancreas in a 61-year-old woman, with an unusual pheno- or genotype detected by histochemical, immunohistochemical, and K- ras oncogene analyses. Histologically, the pancreatic tumor was predominantly composed of clear cell nests with scanty fibrous stroma and scattered duct-like structures. Neither clear cell nor duct-like components of the tumor showed mucin production. Immunohistochemical analysis of neoplastic cells showed a positive reaction to antibodies against cytokeratins 8 and 19, carbohydrate antigen 19-9, and alpha-1-antitrypsin, and showed no reaction to antibodies against carcinoembryonic antigen, neuroendocrine markers, trypsin, amylase, and HMB45. K- ras analysis revealed no mutation at codon 12 in either clear cell or duct-like components. The patient has had no recurrence as yet. The pancreatic carcinoma in our patient may be of duct cell origin, but the results of histochemical, immunohistochemical, and gene analyses and patient's outcome were unusual compared with those of previous cases.

求助全文
通过发布文献求助,成功后即可免费获取论文全文。 去求助
来源期刊
自引率
0.00%
发文量
0
期刊最新文献
Laparoscopic-assisted limited liver resection: technique, indications and results. Laparoscopic major hepato-biliary-pancreatic surgery: formidable challenge to standardization. Tokyo Guidelines for the management of acute cholangitis and cholecystitis. Proceedings of a consensus meeting, April 2006, Tokyo, Japan. Treatment outcome of selective digestive decontamination and enteral nutrition in patients with severe acute pancreatitis. Protective effects of a hibernation-inducer on hepatocyte injury induced by hypothermic preservation.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
现在去查看 取消
×
提示
确定
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术
文献互助 智能选刊 最新文献 互助须知 联系我们:info@booksci.cn
Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。
Copyright © 2023 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1