Location of Repository

Fibroblastic Foci in Usual Interstitial Pneumonia: Idiopathic versus Collagen Vascular Disease

By Kevin R. Flaherty, Thomas V. Colby, William D. Travis, Galen B. Toews, Jeanette A. Mumford, Susan Murray, Victor J. Thannickal, Ella A. Kazerooni, Barry H. Gross, Joseph P. III Lynch and Fernando J. Martinez


A histologic feature of usual interstitial pneumonia is the presence of fibroblastic foci. As some patients with usual interstitial pneumonia and an underlying collagen vascular disease have a better prognosis, we hypothesized that they would have fewer fibroblastic foci. Pathologists reviewed surgical lung biopsies from 108 patients with usual interstitial pneumonia (nine with collagen vascular disease) and assigned a score (absent 0, mild 1, moderate 2, and marked 3) for fibroblastic foci. Patients with idiopathic usual interstitial pneumonia had a higher median profusion of fibroblastic foci (1.75 vs. 1.0, p = 0.003). Baseline characteristics were similar, although patients with a collagen vascular disease were younger, had a shorter duration of symptoms, and had a higher percentage of predicted total lung capacity. Profusion of fibroblastic foci was the most discriminative feature for separating idiopathic from collagen vascular disease–associated usual interstitial pneumonia (odds ratio 8.31; 95% confidence interval, 1.98, 59.42; p = 0.002 for a one-unit increase in fibroblastic foci score). No deaths were noted in the collagen vascular disease–associated usual interstitial pneumonia group; 52 deaths occurred in the idiopathic usual interstitial pneumonia group (log rank; p = 0.005). We conclude that patients with collagen vascular disease–associated usual interstitial pneumonia have fewer fibroblastic foci and improved survival

Topics: Idiopathic Pulmonary Fibrosis, Usual Interstitial Pneumonia, Nonspecific Interstitial Pneumonia, Fibroblastic Focus
Year: 2003
OAI identifier: oai:deepblue.lib.umich.edu:2027.42/91974

Suggested articles


To submit an update or takedown request for this paper, please submit an Update/Correction/Removal Request.