{"title":"Cytokeratin 19 (CK19) as a Tumor Marker in Pleural Effusion","authors":"M. Zaghloul","doi":"10.4172/2329-9088.1000E122","DOIUrl":null,"url":null,"abstract":"Volume 3 • Issue 1 • 1000e122 Trop Med Surg ISSN: 2329-9088 TPMS, an open access journal Pleural effusion is a common clinical presentation. Approximately 20% of pleural effusions are due to malignancy, and 50% of these are due to primary lung cancer [1]. A malignant pleural effusion may be the initial presentation of cancer in 10 to 50% of patients [2]. Cytological examination of malignant effusion is important because it is easy and noninvasive. However, highly suspected cases of malignant effusion with repeated negative cytological findings are sometimes encountered [3]. Several tumor markers in pleural fluid have been evaluated to distinguish malignant effusion from benign e.g. carcinoembryonic antigen (CEA) [4] neuron-specific enolase [5] and cytokeratin 19 [6,7]. During the last 10 years, new immunologic and molecular analytic procedures have been developed to diagnose and characterize minimal residual cancer [8]. Malignant pleural effusions often result from malignant tumors transferring into pleural cavity. On 1998, Lockett et al. [9] had developed keratin-19, c-myc and prolactin inducible protein RT-PCR based method to identify axillary lymph node metastases in patients with breast cancer and thought it appeared to be a readily available and highly sensitive method for detecting breast cancer micrometastases.","PeriodicalId":90756,"journal":{"name":"Tropical medicine & surgery","volume":"3 1","pages":"1-2"},"PeriodicalIF":0.0000,"publicationDate":"2014-10-03","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"8","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Tropical medicine & surgery","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.4172/2329-9088.1000E122","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 8
Abstract
Volume 3 • Issue 1 • 1000e122 Trop Med Surg ISSN: 2329-9088 TPMS, an open access journal Pleural effusion is a common clinical presentation. Approximately 20% of pleural effusions are due to malignancy, and 50% of these are due to primary lung cancer [1]. A malignant pleural effusion may be the initial presentation of cancer in 10 to 50% of patients [2]. Cytological examination of malignant effusion is important because it is easy and noninvasive. However, highly suspected cases of malignant effusion with repeated negative cytological findings are sometimes encountered [3]. Several tumor markers in pleural fluid have been evaluated to distinguish malignant effusion from benign e.g. carcinoembryonic antigen (CEA) [4] neuron-specific enolase [5] and cytokeratin 19 [6,7]. During the last 10 years, new immunologic and molecular analytic procedures have been developed to diagnose and characterize minimal residual cancer [8]. Malignant pleural effusions often result from malignant tumors transferring into pleural cavity. On 1998, Lockett et al. [9] had developed keratin-19, c-myc and prolactin inducible protein RT-PCR based method to identify axillary lymph node metastases in patients with breast cancer and thought it appeared to be a readily available and highly sensitive method for detecting breast cancer micrometastases.