Parra Edwin Roger, Kairalla Ronaldo Adib, de Carvalho Carlos Roberto Ribeiro, Capelozzi Vera Luiza
Department of Pathology, Sao Paulo Medical School, University of São Paulo, Dr Arnaldo Avenue 455, São Paulo 01246-903, Brazil.
Thorax. 2007 May;62(5):428-37. doi: 10.1136/thx.2006.062687. Epub 2007 Jan 24.
Vascular remodelling has recently been shown to be a promising pathogenetic indicator in idiopathic interstitial pneumonias (IIPs).
To validate the importance of the collagen/elastic system in vascular remodelling and to study the relationships between the collagen/elastic system, survival and the major histological patterns of IIPs.
Collagen/elastic system fibres were studied in 25 patients with acute interstitial pneumonia/diffuse alveolar damage, 22 with non-specific interstitial pneumonia/non-specific interstitial pneumonia and 55 with idiopathic pulmonary fibrosis/usual interstitial pneumonia. The Picrosirius polarisation method and Weigert's resorcin-fuchsin histochemistry and morphometric analysis were used to evaluate the amount of vascular collagen/elastic system fibres and their association with the histological pattern of IIPs. The association between vascular remodelling and the degree of parenchymal fibrosis in usual interstitial pneumonia (UIP) was also considered.
The vascular measurement of collagen/elastic fibres was significantly higher in UIP than in the lungs of controls, and in those with diffuse alveolar damage and those with non-specific interstitial pneumonia. In addition, the increment of collagen/elastic fibres in UIP varied according to the degree and activity of the parenchymal fibrosis. The most important predictors of survival in UIP were vascular remodelling classification and vascular collagen deposition.
A progressive vascular fibroelastosis occurs in IIP histological patterns, probably indicating evolutionarily adapted responses to parenchymal injury. The vascular remodelling classification and the increase in vascular collagen were related to survival in IIP and possibly play a role in its pathogenesis. Further studies are needed to determine whether this relationship is causal or consequential.
血管重塑最近被证明是特发性间质性肺炎(IIP)中一个有前景的发病机制指标。
验证胶原/弹性系统在血管重塑中的重要性,并研究胶原/弹性系统、生存率与IIP主要组织学模式之间的关系。
对25例急性间质性肺炎/弥漫性肺泡损伤患者、22例非特异性间质性肺炎/非特异性间质性肺炎患者和55例特发性肺纤维化/普通间质性肺炎患者的胶原/弹性系统纤维进行研究。采用天狼星偏振光法、魏格特间苯二酚品红组织化学法和形态计量分析来评估血管胶原/弹性系统纤维的数量及其与IIP组织学模式的关联。还考虑了普通间质性肺炎(UIP)中血管重塑与实质纤维化程度之间的关联。
UIP中胶原/弹性纤维的血管测量值显著高于对照组、弥漫性肺泡损伤组和非特异性间质性肺炎组的肺部。此外,UIP中胶原/弹性纤维的增加根据实质纤维化的程度和活动情况而有所不同。UIP中生存的最重要预测因素是血管重塑分类和血管胶原沉积。
IIP组织学模式中发生进行性血管纤维弹性组织增生,这可能表明是对实质损伤的进化适应性反应。血管重塑分类和血管胶原增加与IIP的生存相关,并且可能在其发病机制中起作用。需要进一步研究来确定这种关系是因果关系还是结果关系。