B. Fischer et K. Morgenroth, ULTRASTRUCTURAL-STUDY ON HUMAN LUNG IN ALVEOLITIS VERSUS PULMONARY FIBROSIS, The Clinical investigator, 71(6), 1993, pp. 452-460
Lung specimens of 21 patients with diffuse interstitial lung disease w
ere examined. The present ultrastructural study outlines the topograph
y and distribution of inflammatory changes in the interstitium, endoth
elium, and in pneumocytes and phagocytes. Alveolitis is characterized
by marked regenerative activity of type II pneumocytes (cuboid metapla
sia), intraluminal macrophage accumulation, endothelial swelling, mult
ilamination of the. endothelial basement membrane, pericapillary edema
, and primarily by cellular infiltrates in the interstitial space. The
most prominent feature of the interstitium in pulmonary fibrosis is t
he lack of immunoinflammatory cells. In some areas there is a marked a
bsence of alveolar lumen while only a small number of macrophages are
present in the remaining alveolar lumen. Most of the capillaries in th
e fibrous septum have been destroyed. Ultrastructural studies of lung
biopsies in patients with diffuse interstitial lung disease allow the
differentiation between alveolitis and pulmonary fibrosis and thus con
tribute to a therapeutic decision.