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白塞病中的肺部疾病。

Pulmonary disease in Behçet's syndrome.

作者信息

Efthimiou J, Johnston C, Spiro S G, Turner-Warwick M

出版信息

Q J Med. 1986 Mar;58(227):259-80.

PMID:3737870
Abstract

Five patients with Behçet's syndrome presenting with haemoptysis and recurrent radiographic opacities are reported, with a review of 23 similar cases. All 28 cases conformed to a definite clinical pattern with haemoptysis, usually accompanied by pyrexia, chest pain and dyspnoea, being the major feature. Typically pulmonary disease was associated with active disease at other sites, although the patients often only complained of haemoptysis. Patients with Behçet's syndrome and haemoptysis, compared to those without haemoptysis, showed a marked male predominance, with thrombophlebitis and deep vein thrombosis being more common. Rarely pulmonary disease occurred in the absence of one or other of the so called 'major' criteria on which the diagnosis of Behçet's syndrome is usually made, as was so for four of our patients who did not have ocular disease. Immunopathological evidence suggests that the underlying pathogenesis is a pulmonary vasculitis which may result in arterial and venous thromboses, pulmonary infarction, pulmonary haemorrhage and pulmonary arterial aneurysm formation. A role for immune complexes in the pathogenesis of pulmonary disease in Behçet's syndrome is suggested by the finding of circulating immune complexes in association with active pulmonary disease. Corticosteroids were initially helpful in treating active disease in the lungs, and at other sites, in most of the patients in whom they were tried, including our five patients, but serious haemoptysis occasionally recurred, despite further treatment. Four of our patients were initially treated with anticoagulants for a presumed diagnosis of pulmonary embolism, but continued to have haemoptysis. One of these patients subsequently died following massive haemoptysis, despite good anticoagulant control. The haemoptysis in most of the 28 cases was notable for its severity, and in at least 11 (39.3 per cent), pulmonary haemorrhage was the probable cause of death. All deaths due to haemoptysis occurred within six years of the first episode. Whilst pulmonary disease with haemoptysis is infrequent, it carries a very serious prognosis and for this reason correct diagnosis and appropriate treatment is imperative. Pulmonary disease with haemoptysis should be included as one of the so called 'minor' criteria in the diagnosis of Behçet's syndrome.

摘要

本文报告了5例伴有咯血和反复影像学表现为肺部阴影的白塞病患者,并回顾了23例类似病例。所有28例病例均符合一种明确的临床模式,以咯血为主要特征,通常伴有发热、胸痛和呼吸困难。典型的肺部疾病与其他部位的活动性疾病相关,尽管患者通常仅主诉咯血。与无咯血的白塞病患者相比,有咯血的患者男性明显居多,血栓性静脉炎和深静脉血栓更为常见。在缺乏通常用于诊断白塞病的一项或多项所谓“主要”标准的情况下,肺部疾病很少发生,我们的4例患者就没有眼部疾病。免疫病理学证据表明,潜在的发病机制是肺部血管炎,可能导致动脉和静脉血栓形成、肺梗死、肺出血和肺动脉瘤形成。与活动性肺部疾病相关的循环免疫复合物的发现提示免疫复合物在白塞病肺部疾病发病机制中起作用。在大多数接受治疗的患者中,包括我们的5例患者,糖皮质激素最初有助于治疗肺部及其他部位的活动性疾病,但尽管进一步治疗,严重咯血仍偶尔复发。我们的4例患者最初因疑似肺栓塞接受抗凝治疗,但仍有咯血。其中1例患者尽管抗凝控制良好,但随后因大量咯血死亡。28例中的大多数咯血严重,至少11例(39.3%)可能因肺出血死亡。所有咯血导致的死亡均发生在首次发作后的6年内。虽然伴有咯血的肺部疾病不常见,但预后非常严重,因此正确诊断和适当治疗至关重要。伴有咯血的肺部疾病应作为白塞病诊断中所谓“次要”标准之一。

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