Tracheobronchial involvement in Wegener's granulomatosis
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 en...
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Veröffentlicht in: | American journal of respiratory and critical care medicine 1995-02, Vol.151 (2), p.522-526 |
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creator | DAUM, T. E SPECKS, U COLBY, T. V EDELL, E. S BRUTINEL, M. W.F PRAKASH, U. B. S DEREMEE, R. A |
description | 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. |
doi_str_mv | 10.1164/ajrccm.151.2.7842215 |
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E ; SPECKS, U ; COLBY, T. V ; EDELL, E. S ; BRUTINEL, M. W.F ; PRAKASH, U. B. S ; DEREMEE, R. A</creator><creatorcontrib>DAUM, T. E ; SPECKS, U ; COLBY, T. V ; EDELL, E. S ; BRUTINEL, M. W.F ; PRAKASH, U. B. S ; DEREMEE, R. A</creatorcontrib><description>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.</description><identifier>ISSN: 1073-449X</identifier><identifier>EISSN: 1535-4970</identifier><identifier>DOI: 10.1164/ajrccm.151.2.7842215</identifier><identifier>PMID: 7842215</identifier><language>eng</language><publisher>New York, NY: American Lung Association</publisher><subject>Adult ; Aged ; Aged, 80 and over ; Antibodies, Antineutrophil Cytoplasmic ; Autoantibodies - analysis ; Biological and medical sciences ; Bronchi - pathology ; Bronchoscopy ; Female ; Granulomatosis with Polyangiitis - diagnosis ; Granulomatosis with Polyangiitis - immunology ; Granulomatosis with Polyangiitis - pathology ; Humans ; Male ; Medical sciences ; Middle Aged ; Sarcoidosis. Granulomatous diseases of unproved etiology. Connective tissue diseases. Elastic tissue diseases. 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V</creatorcontrib><creatorcontrib>EDELL, E. S</creatorcontrib><creatorcontrib>BRUTINEL, M. W.F</creatorcontrib><creatorcontrib>PRAKASH, U. B. S</creatorcontrib><creatorcontrib>DEREMEE, R. A</creatorcontrib><title>Tracheobronchial involvement in Wegener's granulomatosis</title><title>American journal of respiratory and critical care medicine</title><addtitle>Am J Respir Crit Care Med</addtitle><description>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.</description><subject>Adult</subject><subject>Aged</subject><subject>Aged, 80 and over</subject><subject>Antibodies, Antineutrophil Cytoplasmic</subject><subject>Autoantibodies - analysis</subject><subject>Biological and medical sciences</subject><subject>Bronchi - pathology</subject><subject>Bronchoscopy</subject><subject>Female</subject><subject>Granulomatosis with Polyangiitis - diagnosis</subject><subject>Granulomatosis with Polyangiitis - immunology</subject><subject>Granulomatosis with Polyangiitis - pathology</subject><subject>Humans</subject><subject>Male</subject><subject>Medical sciences</subject><subject>Middle Aged</subject><subject>Sarcoidosis. Granulomatous diseases of unproved etiology. Connective tissue diseases. Elastic tissue diseases. 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V</au><au>EDELL, E. S</au><au>BRUTINEL, M. W.F</au><au>PRAKASH, U. B. S</au><au>DEREMEE, R. A</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Tracheobronchial involvement in Wegener's granulomatosis</atitle><jtitle>American journal of respiratory and critical care medicine</jtitle><addtitle>Am J Respir Crit Care Med</addtitle><date>1995-02-01</date><risdate>1995</risdate><volume>151</volume><issue>2</issue><spage>522</spage><epage>526</epage><pages>522-526</pages><issn>1073-449X</issn><eissn>1535-4970</eissn><abstract>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.</abstract><cop>New York, NY</cop><pub>American Lung Association</pub><pmid>7842215</pmid><doi>10.1164/ajrccm.151.2.7842215</doi><tpages>5</tpages></addata></record> |
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subjects | Adult Aged Aged, 80 and over Antibodies, Antineutrophil Cytoplasmic Autoantibodies - analysis Biological and medical sciences Bronchi - pathology Bronchoscopy Female Granulomatosis with Polyangiitis - diagnosis Granulomatosis with Polyangiitis - immunology Granulomatosis with Polyangiitis - pathology Humans Male Medical sciences Middle Aged Sarcoidosis. Granulomatous diseases of unproved etiology. Connective tissue diseases. Elastic tissue diseases. Vasculitis Trachea - pathology |
title | Tracheobronchial involvement in Wegener's granulomatosis |
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