Organizing pneumonia and pulmonary lymphatic architecture in diffuse alveolar damage

Hum Pathol. 2008 Aug;39(8):1234-8. doi: 10.1016/j.humpath.2008.01.002. Epub 2008 Jul 7.

Abstract

Diffuse alveolar damage represents the pathologic basis of most cases of the acute respiratory distress syndrome. Diffuse alveolar damage reflects injury to the pulmonary alveolar wall and microvasculature, leading to the exudation of water and plasma proteins that can overwhelm the local lymphatic drainage. Organizing pneumonia is a prominent histopathologic feature in some cases of diffuse alveolar damage. We examined whether diffuse alveolar damage-organizing pneumonia and changes in lymphatic architecture might be indicators of clinical outcome in acute respiratory distress syndrome. Formalin-fixed lung sections (n = 26) from thoracoscopic lung biopsies of patients with diffuse alveolar damage in the fibroproliferative phase, with or without organizing pneumonia, were immunostained with anti-CD31 and anti-D240, markers of vascular and lymphatic endothelium, respectively, and examined by morphometric analysis. Positively staining vessels were enumerated and maximal luminal diameters recorded in randomly selected low-power fields. Patients with diffuse alveolar damage-organizing pneumonia showed greater survival than those with diffuse alveolar damage (67% versus 33%, P = .03). The maximal luminal diameter of D240+ lymphatic vessels was larger for diffuse alveolar damage-organizing pneumonia than diffuse alveolar damage (28 +/- 4 versus 59 +/- 16 microm, P = .02). In addition, larger lymphatic luminal diameters (28 +/- 4 versus 47 +/- 11 microm) were associated with increased survival (P = .12). We conclude that lung biopsy histopathology and pulmonary lymphatic morphology may predict survival in acute respiratory distress syndrome.

MeSH terms

  • Adult
  • Aged
  • Aged, 80 and over
  • Female
  • Fibrosis
  • Humans
  • Lung*
  • Lymphatic Vessels / pathology*
  • Male
  • Middle Aged
  • Pneumonia / complications
  • Pneumonia / pathology*
  • Pulmonary Alveoli / pathology*
  • Respiratory Distress Syndrome / complications
  • Respiratory Distress Syndrome / pathology*