Pathologic separation of idiopathic pulmonary fibrosis from fibrotic hypersensitivity pneumonitis

被引:28
|
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 50 条
  • [31] Fibrotic hypersensitivity pneumonitis
    Evans R. Fernández Pérez
    Kevin K. Brown
    [J]. Current Respiratory Care Reports, 2014, 3 (4): : 170 - 178
  • [32] Fibrosis score predicts mortality in patients with fibrotic hypersensitivity pneumonitis
    Oh, Ju Hyun
    Kang, Jieun
    Song, Jin Woo
    [J]. FRONTIERS IN MEDICINE, 2023, 10
  • [33] The Pathogenesis of Chronic Hypersensitivity Pneumonitis in Common With Idiopathic Pulmonary Fibrosis Expression of Apoptotic Markers
    Jinta, Torahiko
    Miyazaki, Yasunari
    Kishi, Masato
    Akashi, Takumi
    Takemura, Tamiko
    Inase, Naohiko
    Yoshizawa, Yasuyuki
    [J]. AMERICAN JOURNAL OF CLINICAL PATHOLOGY, 2010, 134 (04) : 613 - 620
  • [34] Severity of Sleep Disordered Breathing in Patients with Idiopathic Pulmonary Fibrosis and Chronic Hypersensitivity Pneumonitis
    Abdullah, R.
    Kent-Bramer, J.
    Renzoni, E. A.
    Kouranos, V.
    Chua, F. J.
    Kokosi, M.
    Wells, A. U.
    Maher, T. M.
    Man, W.
    Molyneaux, P. L.
    Polkey, M. I.
    George, P. M.
    [J]. AMERICAN JOURNAL OF RESPIRATORY AND CRITICAL CARE MEDICINE, 2018, 197
  • [35] Immunoglobulin free light chains are increased in hypersensitivity pneumonitis and idiopathic pulmonary fibrosis patients
    Kormelink, Groot T.
    Pardo, A.
    Knipping, K.
    Buendia-Roldan, I
    Garcia-de-Alba, C.
    Blokhuis, B.
    Selman, M.
    Redegeld, F.
    [J]. ALLERGY, 2011, 66 : 462 - 462
  • [36] Pathogenesis of chronic hypersensitivity pneumonitis (HP) - differences and similarities to idiopathic pulmonary fibrosis (IPF)
    Wygrecka, M.
    Wujak, L.
    Markart, P.
    [J]. ALLERGOLOGIE, 2017, 40 (07) : 268 - 272
  • [37] Chronic Summer-type Hypersensitivity Pneumonitis: clinical similarities to idiopathic pulmonary fibrosis
    Inase, Naohiko
    Ohtani, Yoshio
    Usui, Yutaka
    Miyazaki, Yasunari
    Takemura, Tamiko
    Yoshizawa, Yasuyuki
    [J]. SARCOIDOSIS VASCULITIS AND DIFFUSE LUNG DISEASES, 2007, 24 (02) : 141 - 147
  • [38] Pulmonary fibrosis in young patients with hypersensitivity pneumonitis
    Elzbieta, Wiatr
    Elzbieta, Radzikowska
    Jacek, Pawlowski
    [J]. SARCOIDOSIS VASCULITIS AND DIFFUSE LUNG DISEASES, 2006, 23 (02) : 149 - 149
  • [39] Pro-Fibrotic Role of IL-17 and Neutrophils in Pulmonary Fibrosis in a Model of Hypersensitivity Pneumonitis
    Kelly, M. M.
    Atkinson, B.
    Maxwell, L.
    Gwozd, C.
    Kubes, P.
    [J]. AMERICAN JOURNAL OF RESPIRATORY AND CRITICAL CARE MEDICINE, 2009, 179
  • [40] Management of fibrotic hypersensitivity pneumonitis
    Mullin, Monica L.
    Churg, Andrew
    Ryerson, Christopher J.
    [J]. CURRENT OPINION IN PULMONARY MEDICINE, 2022, 28 (05) : 421 - 431