a Divisao de Patologia Clinica - Departamento de Patologia, Hospital das Clinicas HCFMUSP, Faculdade de Medicina, Universidade de Sao Paulo , Sao Paulo , BR.
b Laboratorio de Investigacao Medica - LIM 03, Faculdade de Medicina, Universidade de Sao Paulo , Sao Paulo , BR.
Expert Rev Respir Med. 2019 Aug;13(8):747-759. doi: 10.1080/17476348.2019.1637737. Epub 2019 Jul 3.
: Tuberculosis (TB) is the world's leading cause of death from infectious disease. The World Health Organization (WHO) recognized 6.3 million new TB cases in 2017, 16% corresponding to extrapulmonary forms; pleural tuberculosis (PT) is the most common extrapulmonary form in adults. PT diagnosis is often challenging because the scarcity of bacilli in pleural fluid (PF), sometimes requiring invasive procedures to obtain pleural tissue for histological, microbiological or molecular examination. In regions of medium and high disease prevalence, adenosine deaminase (ADA), interferon gamma (IFN-γ) and interleukin 27 (IL-27) dosages are useful to establish presumptive diagnosis in patients with compatible clinical/radiological picture who present with lymphocytic pleural effusion. PT treatment is similar to the pulmonary TB treatment regimen recommended by WHO. : In this update, we present a PT review, including epidemiology, pathogenesis, clinical features, diagnosis, and therapy. : There is no PF test alone accurate for PT diagnosis, despite the evolution in clinical laboratory. ADA, IFN-γ and IL-27 are valuable laboratory biomarkers; however, IFN-γ and IL-27 are quite expensive. Molecular tests present low sensitivity in PF, being useful for diagnostic confirmation. Multidrug therapy remains the PT treatment choice. Advancing research in immunotherapy may bring benefits to PT patients.
结核病(TB)是全球传染病死亡的主要原因。世界卫生组织(WHO)在 2017 年确认了 630 万例新的结核病病例,其中 16%为肺外形式;胸腔结核(PT)是成人中最常见的肺外形式。PT 的诊断通常具有挑战性,因为胸腔液(PF)中细菌的稀缺性,有时需要进行侵入性程序以获取胸腔组织进行组织学、微生物学或分子检查。在中高疾病流行地区,腺苷脱氨酶(ADA)、干扰素γ(IFN-γ)和白细胞介素 27(IL-27)的剂量有助于对具有相容临床/影像学表现且伴有淋巴细胞性胸腔积液的患者建立推定诊断。PT 的治疗与 WHO 推荐的肺结核治疗方案相似。在本次更新中,我们对 PT 进行了综述,包括流行病学、发病机制、临床特征、诊断和治疗。尽管临床实验室取得了进展,但没有一种 PF 检测单独能准确诊断 PT。ADA、IFN-γ 和 IL-27 是有价值的实验室生物标志物;然而,IFN-γ 和 IL-27 非常昂贵。分子检测在 PF 中的敏感性较低,对诊断确认有用。多药治疗仍然是 PT 治疗的选择。免疫疗法的研究进展可能会给 PT 患者带来益处。