Am. J. Respir. Crit. Care Med., Vol 151, No. 2, 02 1995, 522-526.
Tracheobronchial involvement in Wegener's granulomatosis
TE Daum, U Specks, TV Colby, ES Edell, MW Brutinel, UB Prakash and RA DeRemee
Division of Pulmonary and Critical Care Medicine, Mayo Clinic, Rochester, Minnesota 55905.
This study was designed to characterize the clinical spectrum and course of
tracheobronchial involvement in Wegener's granulomatosis (WG). Of the 51
patients with biopsy-proven WG who underwent bronchoscopy at least once at
our institution between January 1982 and November 1993, 30 (59%) had
endobronchial abnormalities due to WG. Initial findings included subglottic
stenosis in five (17%), ulcerating tracheobronchitis with or without
inflammatory pseudotumors in 18 (60%), tracheal or bronchial stenosis
without inflammation in four (13%), and hemorrhage without identifiable
source in two (4%) patients. Nine patients with ulcerating
tracheobronchitis on initial study had subsequent bronchoscopies for
continued symptoms, which in seven cases documented the progression from
ulcerating tracheobronchitis to stenosis without inflammation.
Bronchoscopic interventions included dilation by rigid bronchoscope in
three, YAG-laser treatment in one, and placement of silastic airway stents
in three patients. Only the stents provided persistent airway patency.
Endobronchial biopsies were performed on 21 occasions in 17 patients. Half
of the specimens were helpful in establishing the diagnosis and in all but
three in assessing disease activity. While antineutrophil cytoplasmic
antibody titers reflect overall disease activity, no correlation with
endobronchial inflammatory activity was apparent.
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Copyright © 1995 American Thoracic Society
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