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闭塞性细支气管炎机化性肺炎(BOOP)。一种解剖临床实体的特征与界限

[Bronchiolitis obliterans organizing pneumonia (BOOP). Characteristics and boundaries of an anatomo-clinical entity].

作者信息

Cordier J F, Loire R, Peyrol S

机构信息

Service de Pneumologie, Hôpital Cardiovasculaire et Pneumologique Louis-Pradel, Lyon.

出版信息

Rev Mal Respir. 1991;8(2):139-52.

PMID:1857810
Abstract

Bronchiolitis obliterans organizing pneumonia (BOOP) is defined by endoluminal obstruction of distal airspaces by a fibrous granulation tissue consisting of inflammatory cells, fibroblasts, and connective tissue. The morphogenesis of the process is the following: diffuse alveolar injury leading to basement membrane denudation and intra-alveolar exudate of fibrinogen, immunoglobulins, coagulation factors, fibronectin; intra-alveolar migration of interstitial fibroblasts through gaps of the epithelial basement membrane; intra-alveolar secretion of loose connective tissue (codistribution of collagens I, III, V, and fibronectin) by the fibroblasts-myofibroblasts. The main characteristic of this peculiar fibrosis is its possible reversibility. BOOP is not specific for any aetiology, and it is found in various conditions as infectious diseases, drug induced pulmonary diseases, connective tissue diseases. It is also present in other conditions where it is not the most contributive information to diagnosis (hypersensitivity pneumonitis, chronic eosinophilic pneumonia). But in some cases BOOP remains idiopathic and has to be individualized. Three clinical and imaging profiles are distinguished: the most characteristic consists of an inflammatory context with imaging patchy alveolar opacities, migrating and relapsing, and most steroid sensitive; the other two presentations are less remarkable: pseudo-neoplastic localized chronic pneumonia, and diffuse infiltrative lung disease. BOOP is a clinico-pathologic entity that the clinician must know because of the efficacy of corticosteroid treatment in most cases, and it further represents an unique model to understand the pathogenesis of fibrosing pulmonary diseases.

摘要

机化性细支气管炎伴机化性肺炎(BOOP)的定义为,终末气腔内被由炎症细胞、成纤维细胞和结缔组织构成的纤维肉芽组织阻塞。该病变的形态发生过程如下:弥漫性肺泡损伤导致基底膜剥脱以及肺泡内出现纤维蛋白原、免疫球蛋白、凝血因子和纤连蛋白的渗出物;间质成纤维细胞通过上皮基底膜的间隙向肺泡内迁移;成纤维细胞-肌成纤维细胞在肺泡内分泌疏松结缔组织(I、III、V型胶原蛋白和纤连蛋白共同分布)。这种特殊纤维化的主要特征是其可能具有可逆性。BOOP并非由任何特定病因引起,在多种情况下均可出现,如感染性疾病、药物性肺疾病、结缔组织病。在其他一些疾病中也可出现BOOP,但它并非诊断的最关键信息(如过敏性肺炎、慢性嗜酸性粒细胞性肺炎)。但在某些情况下,BOOP仍为特发性,必须进行个体化诊断。可区分出三种临床和影像学表现:最具特征性的表现为炎症背景下出现影像学上的斑片状肺泡实变,病变游走且反复出现,对类固醇最为敏感;另外两种表现则不太典型:假肿瘤性局限性慢性肺炎和弥漫性浸润性肺疾病。BOOP是一种临床病理实体,临床医生必须了解,因为在大多数情况下皮质类固醇治疗有效,而且它还是理解纤维化性肺疾病发病机制的独特模型。

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