Pulmonary vascular lesions in end-stage idiopathic pulmonary fibrosis:: histopathologic study on lung explant specimens and correlations with pulmonary hemodynamics

被引:101
作者
Colombat, Magali
Mal, Herve
Groussard, Odile
Capron, Frederique
Thabut, Gabriel
Jebrak, Gilles
Brugiere, Olivier
Dauriat, Gaelle
Castier, Yves
Leseche, Guy
Fournier, Michel
机构
[1] Hop Beaujon, Dept Pathol, F-92110 Clichy, France
[2] Hop Beaujon, Dept Pneumol, F-92110 Clichy, France
[3] Hop La Pitie Salpetriere, Dept Pathol, F-75013 Paris, France
[4] Hop Beaujon, Dept Thorac & Cardiovasc Surg, F-92110 Clichy, France
关键词
idiopathic pulmonary fibrosis; pulmonary hypertension; occlusive venopathy; lung transplantation;
D O I
10.1016/j.humpath.2006.06.007
中图分类号
R36 [病理学];
学科分类号
100104 ;
摘要
In patients presenting with idiopathic pulmonary fibrosis (IPF), modifications of pulmonary vessels are well defined in fibrotic areas but have not been accurately assessed in the intervening patches of preserved lung. Moreover, the relation between pulmonary vessel lesions and pulmonary hemodynamics is not well known. We therefore designed a retrospective study on lung explant specimens from 26 patients with a firm diagnosis of IPF who had undergone lung transplantation. Our aim was to (1) describe the vascular lesions, especially in preserved lung areas, and (2) correlate them with pulmonary hemodynamics. In dense fibrotic zones, thickening of the arterial and venous wall with severe luminal narrowing was present in each patient. In architecturally preserved lung zones, occlusion of venules and small pulmonary veins was observed in 65% of the patients, although there were only mild changes of muscular pulmonary arteries. We found a significant positive correlation between the macroscopic extent of lung fibrosis and mean pulmonary artery pressure, but we failed to find a relation between mean pulmonary artery pressure and venous/venular lesions in nonfibrotic areas. Our study points out that in many patients with IPF, nonfibrotic lung areas demonstrate an occlusive venopathy, the signification of which remains undetermined. (c) 2007 Elsevier Inc. All rights reserved.
引用
收藏
页码:60 / 65
页数:6
相关论文
共 21 条
  • [1] American Thoracic Society/European Respiratory Society International Multidisciplinary Consensus Classification of the Idiopathic Interstitial Pneumonias, 2002, Am J Respir Crit Care Med, V165, P277, DOI [DOI 10.1164/AJRCCM.165.2.ATS01, 10.1164/ajrccm.165.2.ats01]
  • [2] DAIL DH, 1987, PULMONARY PATHOLOGY, P483
  • [3] Dorfmüller P, 2003, SARCOIDOSIS VASC DIF, V20, P9
  • [4] Heterogeneous increase in CD34-positive alveolar capillaries in idiopathic pulmonary fibrosis
    Ebina, M
    Shimizukawa, M
    Shibata, N
    Kimura, Y
    Suzuki, T
    Endo, M
    Sasano, H
    Kondo, T
    Nukiwa, T
    [J]. AMERICAN JOURNAL OF RESPIRATORY AND CRITICAL CARE MEDICINE, 2004, 169 (11) : 1203 - 1208
  • [5] Primary pulmonary hypertension -: Insights into pathogenesis from epidemiology
    Galiè, N
    Manes, A
    Uguccioni, L
    Serafini, F
    De Rosa, M
    Branzi, A
    Magnani, B
    [J]. CHEST, 1998, 114 (03) : 184S - 194S
  • [6] Medical progress: Idiopathic pulmonary fibrosis.
    Gross, TJ
    Hunninghake, GW
    [J]. NEW ENGLAND JOURNAL OF MEDICINE, 2001, 345 (07) : 517 - 525
  • [7] HAMMAR SP, 1987, PULMONARY PATHOLOGY, P483
  • [8] HAWRYLKIEWICZ I, 1982, B EUR PHYSIOPATH RES, V18, P403
  • [9] Idiopathic pulmonary fibrosis - Clinical relevance of pathologic classification
    Katzenstein, ALA
    Myers, JL
    [J]. AMERICAN JOURNAL OF RESPIRATORY AND CRITICAL CARE MEDICINE, 1998, 157 (04) : 1301 - 1315
  • [10] KATZENSTEIN ALA, 1997, KATZENSTEIN ASKINS S, P48