Ezri T, Kunichezky S, Eliraz A, Soroker D, Halperin D, Schattner A
Department of Anaesthesiology, Kaplan Hospital, Rehovot, Israel.
Q J Med. 1994 Jan;87(1):1-10. doi: 10.1093/oxfordjournals.qjmed.a068855.
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.
我们回顾了关于闭塞性细支气管炎(BO)患者临床表现、诊断和治疗的当前概念,重点关注临床/病理相关性及近期进展。BO是一种相对罕见的疾病,但其发病率可能高于普遍认知,且呈持续上升趋势,部分原因是识别能力提高,也由于接触工业烟雾增多以及在肺移植中的发生。BO的组织学特征是呼吸细支气管腔被机化结缔组织不同程度地闭塞,常延伸至肺泡(“增殖性”BO伴机化性肺炎——BOOP),或近端传导性细支气管出现更广泛的纤维化和瘢痕形成(“缩窄性”BO)。多种临床情况与BO的发生有关,尤其是病毒和支原体感染、接触有毒烟雾以及在胶原血管病、药物反应或器官移植背景下的免疫反应。BO的临床病程和特征可能因病因、组织学模式和疾病阶段而有很大差异。最常见的表现是进行性干咳和呼吸困难,胸部X线显示弥漫性斑片状间质性肺浸润。在病情更严重的病例中,肺功能检查根据肺泡受累程度显示限制性或阻塞性缺陷,且有低氧血症而无二氧化碳潴留。通常根据临床情况即可做出诊断,然而,对于重症患者,应通过组织诊断(最好是开胸肺活检)来消除不确定性。治疗基于对症治疗。使用皮质类固醇存在争议,但很常见。BOOP患者较为特殊,可能不存在潜在疾病(“特发性”BOOP或隐源性机化性肺炎——COP),通常存在限制性通气缺陷,对皮质类固醇的反应往往显著。