Idiopathic fibrosing alveolitis: a review with emphasis on ultrastructural and immunohistochemical features
- PMID: 2418565
- DOI: 10.3109/01913128509074587
Idiopathic fibrosing alveolitis: a review with emphasis on ultrastructural and immunohistochemical features
Abstract
Fibrosing alveolitis is a usually chronic pulmonary disease affecting middle-aged men and women and causing progressive dyspnea. This review discusses the nosologic, etiologic, immunopathogenic, histologic, immunohistochemical and ultrastructural features of this condition. A hypothesis is presented suggesting microvascular damage as the primary pathologic change in cases associated with collagen vascular diseases and viral pneumonia.
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