细胞角蛋白19 (CK19)作为胸腔积液的肿瘤标志物

M. Zaghloul
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引用次数: 8

摘要

胸膜积液是一种常见的临床表现,是一种开放获取的期刊。大约20%的胸腔积液是由恶性肿瘤引起的,其中50%是由原发性肺癌[1]引起的。恶性胸腔积液可能是10 - 50%的bbb患者癌症的最初表现。恶性积液的细胞学检查是重要的,因为它是简单和无创的。然而,高度怀疑恶性积液并反复出现阴性细胞学结果的病例有时会遇到[3]。已经评估了胸膜液中几种肿瘤标志物来区分恶性积液和良性积液,如癌胚抗原(CEA)[4],神经元特异性烯醇化酶[5]和细胞角蛋白19[6,7]。在过去的十年中,新的免疫学和分子分析方法已经发展到诊断和表征微小残留癌bbb。恶性胸腔积液多因恶性肿瘤转移至胸腔所致。1998年,Lockett等人([9])开发了基于角蛋白-19、c-myc和催乳素诱导蛋白RT-PCR的方法来鉴别乳腺癌患者腋窝淋巴结转移,并认为这似乎是一种容易获得且高度敏感的检测乳腺癌微转移的方法。
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Cytokeratin 19 (CK19) as a Tumor Marker in Pleural Effusion
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.
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