Haider Al-Najjar , Matthew Evison , Helen Doran , Richard Booton , Paul Taylor
{"title":"原发性肺类肝腺癌1例","authors":"Haider Al-Najjar , Matthew Evison , Helen Doran , Richard Booton , Paul Taylor","doi":"10.1016/j.ctrc.2015.10.001","DOIUrl":null,"url":null,"abstract":"<div><p>We herein report a case of primary pulmonary hepatoid adenocarcinoma in a 71 year old man and provide an overview on knowledge and existing reports of this rare tumour. Primary pulmonary hepatoid adenocarcinoma is an AFP-producing lung tumour composed of neoplastic cells morphologically resembling hepatocellular carcinoma. The main challenge for physicians encountering such tumours is distinguishing between hepatocellular carcinomas and pulmonary hepatoid adenocarcinomas. Previous literature is conflicting, particularly around the distinguishing immunohistochemical characteristics of the two tumours. Given the rarity of this tumour and paucity of published literature, we believe the clinical–radiological characteristics provide the key to diagnosis and aim to demonstrate this in our case.</p></div>","PeriodicalId":90461,"journal":{"name":"Cancer treatment communications","volume":null,"pages":null},"PeriodicalIF":0.0000,"publicationDate":"2015-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1016/j.ctrc.2015.10.001","citationCount":"10","resultStr":"{\"title\":\"Primary pulmonary hepatoid adenocarcinoma: A case report\",\"authors\":\"Haider Al-Najjar , Matthew Evison , Helen Doran , Richard Booton , Paul Taylor\",\"doi\":\"10.1016/j.ctrc.2015.10.001\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><p>We herein report a case of primary pulmonary hepatoid adenocarcinoma in a 71 year old man and provide an overview on knowledge and existing reports of this rare tumour. Primary pulmonary hepatoid adenocarcinoma is an AFP-producing lung tumour composed of neoplastic cells morphologically resembling hepatocellular carcinoma. The main challenge for physicians encountering such tumours is distinguishing between hepatocellular carcinomas and pulmonary hepatoid adenocarcinomas. Previous literature is conflicting, particularly around the distinguishing immunohistochemical characteristics of the two tumours. Given the rarity of this tumour and paucity of published literature, we believe the clinical–radiological characteristics provide the key to diagnosis and aim to demonstrate this in our case.</p></div>\",\"PeriodicalId\":90461,\"journal\":{\"name\":\"Cancer treatment communications\",\"volume\":null,\"pages\":null},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2015-01-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://sci-hub-pdf.com/10.1016/j.ctrc.2015.10.001\",\"citationCount\":\"10\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Cancer treatment communications\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/S2213089615300220\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Cancer treatment communications","FirstCategoryId":"1085","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S2213089615300220","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
Primary pulmonary hepatoid adenocarcinoma: A case report
We herein report a case of primary pulmonary hepatoid adenocarcinoma in a 71 year old man and provide an overview on knowledge and existing reports of this rare tumour. Primary pulmonary hepatoid adenocarcinoma is an AFP-producing lung tumour composed of neoplastic cells morphologically resembling hepatocellular carcinoma. The main challenge for physicians encountering such tumours is distinguishing between hepatocellular carcinomas and pulmonary hepatoid adenocarcinomas. Previous literature is conflicting, particularly around the distinguishing immunohistochemical characteristics of the two tumours. Given the rarity of this tumour and paucity of published literature, we believe the clinical–radiological characteristics provide the key to diagnosis and aim to demonstrate this in our case.