Pathologic separation of idiopathic pulmonary fibrosis from fibrotic hypersensitivity pneumonitis

被引:31
作者
Wright, Joanne L. [1 ,2 ]
Churg, Andrew [1 ,3 ]
Hague, Cameron J. [4 ]
Wong, Alyson [5 ,6 ]
Ryerson, Christopher J. [5 ,6 ]
机构
[1] Univ British Columbia, Dept Pathol, Vancouver, BC, Canada
[2] St Pauls Hosp, Vancouver, BC, Canada
[3] Vancouver Gen Hosp, Vancouver, BC, Canada
[4] St Pauls Hosp, Dept Radiol, Vancouver, BC, Canada
[5] Univ British Columbia, Dept Med, Vancouver, BC, Canada
[6] St Pauls Hosp, Ctr Heart Lung Innovat, Vancouver, BC, Canada
关键词
INTERSTITIAL PNEUMONIA; INTEROBSERVER AGREEMENT; DIAGNOSTIC-CRITERIA; LUNG-DISEASE; DIFFERENTIATION; TISSUE;
D O I
10.1038/s41379-019-0389-3
中图分类号
R36 [病理学];
学科分类号
100104 ;
摘要
Accurate separation of idiopathic pulmonary fibrosis from fibrotic (chronic) hypersensitivity pneumonitis is crucial to patient management, but is frequently a difficult problem. Our objective was to identify pathologic variables that help make this separation. Clinical, radiological, and pathologic data were re-reviewed for 23 patients with a fibrotic interstitial lung disease and biopsy suggesting idiopathic pulmonary fibrosis or fibrotic hypersensitivity pneumonitis. Clinical features, high-resolution computed tomography, and surgical lung biopsies were each examined independently using a prespecified approach. This was followed by a multidisciplinary discussion in which the likelihood of an idiopathic pulmonary fibrosis diagnosis was assigned by the clinician alone based only on clinical data, by the clinician and radiologist based on integrated clinical and radiologic data, and by the clinician, radiologist, and pathologist based on all three domains. A higher multidisciplinary discussion-based confidence of idiopathic pulmonary fibrosis was associated with older age at diagnosis, male sex, higher forced vital capacity, and absence of ground glass changes. Pathologic variables associated with a higher multidisciplinary discussion-based confidence of idiopathic pulmonary fibrosis included increased number of fibroblast foci/cm(2) and increased subpleural fibrosis. Pathologic variables associated with a higher multidisciplinary discussion-based confidence of hypersensitivity pneumonitis included an increased fraction of bronchioles with peribronchiolar metaplasia, increased foci of peribronchiolar metaplasia/cm(2), and presence of giant cells/granulomas. These results provide guidance in separating idiopathic pulmonary fibrosis from hypersensitivity pneumonitis; however, a third of cases could not be confidently classified even when using these pathologic features combined with clinical and radiologic information in a multidisciplinary discussion.
引用
收藏
页码:616 / 625
页数:10
相关论文
共 20 条
[1]   LUNG MORPHOMETRY - A NEW-GENERATION OF TOOLS AND EXPERIMENTS FOR ORGAN, TISSUE, CELL, AND MOLECULAR-BIOLOGY [J].
BOLENDER, RP ;
HYDE, DM ;
DEHOFF, RT .
AMERICAN JOURNAL OF PHYSIOLOGY, 1993, 265 (06) :L521-L548
[2]  
Churg A, 2017, AM J SURG PATHOL, V41, P1403, DOI 10.1097/PAS.0000000000000885
[3]   Pathology of Chronic Hypersensitivity Pneumonitis What Is It? What Are the Diagnostic Criteria? Why Do We Care? [J].
Churg, Andrew ;
Bilawich, AnaMaria ;
Wright, Joanne L. .
ARCHIVES OF PATHOLOGY & LABORATORY MEDICINE, 2018, 142 (01) :109-119
[4]   Pathologic Patterns and Survival in Chronic Hypersensitivity Pneumonitis [J].
Churg, Andrew ;
Sin, Don D. ;
Everett, Douglas ;
Brown, Kevin ;
Cool, Carlyne .
AMERICAN JOURNAL OF SURGICAL PATHOLOGY, 2009, 33 (12) :1765-1770
[5]   An official European Respiratory Society/American Thoracic Society research statement: interstitial pneumonia with autoimmune features [J].
Fischer, Aryeh ;
Antoniou, Katerina M. ;
Brown, Kevin K. ;
Cadranel, Jacques ;
Corte, Tamera J. ;
du Bois, Roland M. ;
Lee, Joyce S. ;
Leslie, Kevin O. ;
Lynch, David A. ;
Matteson, Eric L. ;
Mosca, Marta ;
Noth, Imre ;
Richeldi, Luca ;
Strek, Mary E. ;
Swigris, Jeffrey J. ;
Wells, Athol U. ;
West, Sterling G. ;
Collard, Harold R. ;
Cottin, Vincent .
EUROPEAN RESPIRATORY JOURNAL, 2015, 46 (04) :976-987
[6]   Idiopathic interstitial pneumonia - What is the effect of a multidisciplinary approach to diagnosis? [J].
Flaherty, KR ;
King, TE ;
Raghu, G ;
Lynch, JP ;
Colby, TV ;
Travis, WD ;
Gross, BH ;
Kazerooni, EA ;
Toews, GB ;
Long, Q ;
Murray, S ;
Lama, VN ;
Gay, SE ;
Martinez, FJ .
AMERICAN JOURNAL OF RESPIRATORY AND CRITICAL CARE MEDICINE, 2004, 170 (08) :904-910
[7]   Heterogeneity in Unclassifiable Interstitial Lung Disease A Systematic Review and Meta-Analysis [J].
Guler, Sabina A. ;
Ellison, Kina ;
Algamdi, Mohmmed ;
Collard, Harold R. ;
Ryerson, Christopher J. .
ANNALS OF THE AMERICAN THORACIC SOCIETY, 2018, 15 (07) :854-863
[8]   Interobserver Agreement of Usual Interstitial Pneumonia Diagnosis Correlated With Patient Outcome [J].
Hashisako, Mikiko ;
Tanaka, Tomonori ;
Terasaki, Yasuhiro ;
Uekusa, Toshimasa ;
Achcar, Rosane D. ;
Aswad, Bassam I. ;
Bamefleh, Hanaa S. ;
Capelozzi, Vera L. ;
English, John C. ;
Fabro, Alexandre T. ;
Kataoka, Kensuke ;
Hayashi, Tomayoshi ;
Kondoh, Yasuhiro ;
Taniguchi, Hiroyuki ;
Fukuoka, Junya .
ARCHIVES OF PATHOLOGY & LABORATORY MEDICINE, 2016, 140 (12) :1375-1382
[9]   Diagnostic criteria for idiopathic pulmonary fibrosis: a Fleischner Society White Paper [J].
Lynch, David A. ;
Sverzellati, Nicola ;
Travis, William D. ;
Brown, Kevin K. ;
Colby, Thomas V. ;
Galvin, Jeffrey R. ;
Goldin, Jonathan G. ;
Hansell, David M. ;
Inoue, Yoshikazu ;
Johkoh, Takeshi ;
Nicholson, Andrew G. ;
Knight, Shandra L. ;
Raoof, Suhail ;
Richeldi, Luca ;
Ryerson, Christopher J. ;
Ryu, Jay H. ;
Wells, Athol U. .
LANCET RESPIRATORY MEDICINE, 2018, 6 (02) :138-153
[10]   Chronic hypersensitivity pneumonitis in patients diagnosed with idiopathic pulmonary fibrosis: a prospective case-cohort study [J].
Morell, Ferran ;
Villar, Ana ;
Montero, Maria-Angeles ;
Munoz, Xavier ;
Colby, Thomas V. ;
Pipvath, Sudhakar ;
Cruz, Maria-Jesus ;
Raghu, Ganesh .
LANCET RESPIRATORY MEDICINE, 2013, 1 (09) :685-694