甲氨蝶呤引起的肺炎:支气管肺泡灌洗的异质性和癌症与类风湿关节炎的差异。

Tommaso D'Elia
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引用次数: 17

摘要

目的:我们对甲氨蝶呤引起的肺炎(MTX-P)的支气管肺泡灌洗(BAL)的了解是不完整的,并且基于有时明显相互矛盾的数据。本综述的目的是对迄今为止发表的病例中MTX-P的BAL特征提供一个全面的概述,并确定癌症和类风湿关节炎患者之间的细胞学模式和任何差异,这两个患者亚群中更常发生这种并发症。方法:通过PUBMED、EMBASE等数据库系统检索2013年11月前发表的英文文章。经证实诊断为MTX-P并仔细提及每个BAL参数的成年患者进行了检查。结果:17篇文章共纳入47例患者。四种BAL伴不同合并淋巴细胞增多症,两种伴明显嗜中性粒细胞增多症。与类风湿关节炎患者相比,癌症患者淋巴细胞增生更强烈(P=0.004), CD4/CD8比值更低(P=0.01)。结论:在MTX-P中,BAL的细胞学分析可能揭示多达六种不同的模式。在MTX-P影响的癌症患者中,BAL倾向于表现出典型的超敏性肺炎特征,而在类风湿关节炎患者中,BAL更具有异质性,淋巴细胞增生不那么强烈,中性粒细胞增多更明显,CD4/CD8比值更高。这些差异可能与两种背景疾病之间肺部基线状况的差异有关,即癌症患者先前健康的肺和类风湿性关节炎患者已经受到免疫介导的炎症过程影响的肺,通常不明显。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Methotrexate-induced pneumonitis: heterogeneity of bronchoalveolar lavage and differences between cancer and rheumatoid arthritis.
PURPOSE Our knowledge on bronchoalveolar lavage (BAL) of methotrexate-induced pneumonitis (MTX-P) is fragmentary and based on data that are sometimes apparently conflicting. Aim of this review was to provide a comprehensive overview on the BAL features of MTX-P arising from cases published to date, and to determine the cytological patterns and any differences between cancer and rheumatoid arthritis patients, the two patient subsets among which this complication more often occurs. METHODS English-language articles published up to November 2013 were systematically searched through PUBMED, EMBASE, and other databases. Adult patients with a proven diagnosis of MTX-P and careful mention of each BAL parameter were examined. RESULTS Seventeen articles for a total of 47 patients were included. Four BAL patterns with a variably combined lymphocytosis and two with prominent neutrophilia were identified. A more intense lymphocytosis (P=0.004) and a more depressed CD4/CD8 ratio (P=0.01) were found in cancer patients compared with rheumatoid arthritis patients. CONCLUSIONS In MTX-P, cytological analysis of BAL may disclose up to six different patterns. In MTX-P affecting cancer patients, BAL tends to show the typical features of hypersensitivity pneumonitis, while, in rheumatoid arthritis patients, it is more heterogeneous, with a less intense lymphocytosis, a more pronounced neutrophilia, and a higher CD4/CD8 ratio. These differences could be related to a disparity in baseline pulmonary conditions between the two background diseases, i.e., to the presence of previously healthy lungs in cancer patients, and lungs already involved by the immune-mediated inflammatory processes, often not manifestly, in rheumatoid arthritis patients.
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