闭塞性细支气管炎——当前概念。

Quarterly Journal of Medicine Pub Date : 1994-01-01
T Ezri, S Kunichezky, A Eliraz, D Soroker, D Halperin, A Schattner
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引用次数: 0

摘要

我们回顾了目前关于闭塞性细支气管炎(BO)的临床表现、诊断和治疗的概念,重点介绍了临床/病理相关性和最新进展。BO是一种相对罕见的疾病,但它的发病率可能比一般认为的要高,而且还在不断上升,部分原因是人们对它的认识有所提高,但也有一部分原因是接触工业烟雾的增加,以及它在肺移植中的发生。BO在组织学上的特征是通过组织结缔组织经常延伸到肺泡(“增殖性”BO伴组织性肺炎—BOOP)或更近端、传导性细支气管更广泛的纤维化和瘢痕形成(“收缩性”BO),导致呼吸性细支气管管腔不同程度的闭塞。不同的临床条件与BO的发生有关,特别是病毒和支原体感染、有毒烟雾暴露和胶原血管疾病、药物反应或器官移植的免疫反应。BO的临床病程和特征可能根据疾病的病因、组织学模式和分期而有很大的不同。最常见的表现是进行性干咳和呼吸困难,胸片上伴有弥漫性斑片状肺间质浸润。在较晚期的病例中,肺功能检查显示限制性或阻塞性缺陷(取决于肺泡受累程度)和无二氧化碳潴留的低氧血症。临床诊断通常是可能的,然而,对于病情严重的患者,不确定性应通过组织诊断来解决,最好是通过开放式肺活检。治疗以对症治疗为基础。皮质类固醇的使用是有争议的,但很常见。BOOP患者是特殊的,因为可能没有潜在的疾病(“特发性”BOOP或隐源性组织性肺炎—COP),限制性通气缺陷是常见的,对皮质类固醇的反应通常是显著的。
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Bronchiolitis obliterans--current concepts.

We review current concepts about the clinical manifestations, diagnosis and treatment of patients with bronchiolitis obliterans (BO) with emphasis on clinical/pathological correlations and recent developments. BO is a relatively rare disease, but its incidence is probably higher than generally believed and is continuously rising, partly because of better recognition, but also because of increased exposure to industrial fumes, and its occurrence in lung transplantation. BO is characterized histologically by varying degrees of obliteration of the lumen of the respiratory bronchioles by organizing connective tissue often extending into the alveoli ('proliferative' BO with organizing pneumonia--BOOP) or by more extensive fibrosis and scarring of the more proximal, conductive bronchioles ('constrictive' BO). Diverse clinical conditions have been associated with the development of BO, notably viral and mycoplasma infection, toxic fume exposure and immune reactions in the setting of a collagen vascular disease, drug reaction or organ transplantation. The clinical course and features of BO may vary considerably according to the aetiology, histological pattern and stage of the disease. The most common presentation is that of a progressive dry cough and dyspnea, associated with diffuse patchy interstitial lung infiltrates on chest X-ray. In the more advanced cases, lung function tests show either restrictive or obstructive defects, depending on the extent of alveolar involvement, and hypoxemia without CO2 retention. The diagnosis is often possible on clinical grounds, however, in a seriously ill patient uncertainty should be resolved by tissue diagnosis, preferably by open lung biopsy. Treatment is based on symptomatic therapy. The use of corticosteroids is controversial, but common. Patients with BOOP are exceptional, in that there may be no underlying condition ('idiopathic' BOOP or cryptogenic organizing pneumonia--COP), a restrictive ventilatory defect is usual and the response to corticosteroids often remarkable.

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