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特发性肺纤维化患者支气管肺泡灌洗液中的癌胚抗原

Carcinoembryonic antigen in bronchoalveolar lavage fluid in patients with idiopathic pulmonary fibrosis.

作者信息

Takahashi H, Nukiwa T, Matsuoka R, Danbara T, Natori H, Arai T, Kira S

出版信息

Jpn J Med. 1985 Aug;24(3):236-43. doi: 10.2169/internalmedicine1962.24.236.

Abstract

An increased incidence of lung cancer and epithelial metaplasia or hyperplasia which is felt to be as a precursor of cancer, has been reported in patients with idiopathic pulmonary fibrosis (IPF). In this study, carcinoembryonic antigen (CEA) in bronchoalveolar lavage (BAL) fluid was measured in 53 control patients, 31 patients with sarcoidosis, 10 patients with hypersensitivity pneumonitis, 16 patients with primary lung cancer and 26 patients with histologically confirmed IPF. High ratio of CEA to albumin (Alb), exceeding mean + 2SD of nonsmoking control patients, were found in 8 (25%) out of 32 smoking control patients, 4 (44%) out of 9 nonsmoking patients with IPF, 8 (62%) out of 13 smoking patients with IPF, 3 (75%) out of 4 smoking patients with IPF and lung cancer and 13 (81%) out of 16 patients with primary lung cancer, although BAL was performed at the noncancerous parts of the lung in the cases of lung cancer. Furthermore, it was confirmed that CEA increased in BAL fluid in these subjects were different from nonspecific cross-reacting antigen (NCA) which was detectable in the normal lung. Thus we consider that the increase of CEA/Alb ratio in BAL fluid is a possible marker of these early histological disorders in the lung, and also suggests a greater risk of malignant change in the clinical course of IPF.

摘要

据报道,特发性肺纤维化(IPF)患者肺癌、上皮化生或增生(被认为是癌症的前兆)的发病率有所增加。在本研究中,对53名对照患者、31名结节病患者、10名过敏性肺炎患者、16名原发性肺癌患者和26名经组织学确诊的IPF患者的支气管肺泡灌洗(BAL)液中的癌胚抗原(CEA)进行了测量。在32名吸烟对照患者中有8名(25%)、9名不吸烟的IPF患者中有4名(44%)、13名吸烟的IPF患者中有8名(62%)、4名患有IPF和肺癌的吸烟患者中有3名(75%)以及16名原发性肺癌患者中有13名(81%)的BAL液中CEA与白蛋白(Alb)的比值高于不吸烟对照患者的均值+2SD,尽管在肺癌患者中BAL是在肺部的非癌部位进行的。此外,已证实这些受试者BAL液中CEA的升高与正常肺中可检测到的非特异性交叉反应抗原(NCA)不同。因此,我们认为BAL液中CEA/Alb比值的升高可能是肺部这些早期组织学病变的一个标志物,也提示IPF临床过程中发生恶性变化的风险更大。

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