Idiopathic interstitial fibrosis.

Abstract:

:The lung has only a limited pattern of response to injury. Idiopathic interstitial fibrosis is a descriptive term, describing the end stage of one pattern of pulmonary fibrosis in which the inflammation lies within the structure of the alveolar walls and around vessels and bronchioli, in the interstitium. The disease is characteristically subpleural in distribution and provides a marked restrictive consequence on pulmonary function which progresses to hypoxic core pulmonale. This is despite the apparent normality of much of the lung at autopsy. Six to fifteen percent develop lung cancer, the proportion depending on the autopsy rate. A nonspecific nature of the changes limits the diagnostic value of transbronchial biopsy, open lung biopsy may be of value in assessing and grading the disease in relationship to therapy.

journal_name

Lung

journal_title

Lung

authors

Lambe D

doi

10.1007/BF02718237

subject

Has Abstract

pub_date

1990-01-01 00:00:00

pages

993-7

eissn

0341-2040

issn

1432-1750

journal_volume

168 Suppl

pub_type

杂志文章

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