PEDIATRICS Vol. 101 No. 1 January 1998, pp. 82-85
Received Feb 19, 1997; accepted May 15, 1997.
,
From the * Pediatric Pulmonary Section and
Academic General
Pediatric Section, Department of Pediatrics, Baylor College of
Medicine, Houston, Texas; the § Pediatric Pulmonary Section, Department
of Pediatrics, University of Colorado Health Sciences Center, and
National Jewish Medical and Research Center, Denver, Colorado.
Objective. To evaluate the value of a systematic approach to the diagnosis of pediatric interstitial lung disease (ILD).
Methods. In this descriptive, observational, prospective study, we evaluated 51 children presenting with ILD of unknown etiology during a 3-year period. Specific clinical information regarding history, physical examination, diagnostic evaluation, and final diagnosis was recorded on each patient.
Results. A specific diagnosis was established by history and physical examination alone in 1 patient, noninvasive tests alone in 8 others, and invasive tests, including lung biopsy, in another 26. Of the remaining patients, 8 had a suggestive diagnosis, and 8 had no specific diagnosis.
Conclusions. A systematic approach to the diagnosis of pediatric ILD is useful, and not all patients need lung biopsy for diagnosis.
Key words: interstitial lung disease, pulmonary fibrosis, children.
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