Pathological features of connective tissue disease-associated interstitial lung disease in transbronchial cryobiopsies
Language English Country England, Great Britain Media print-electronic
Document type Journal Article
PubMed
39223069
DOI
10.1111/his.15311
Knihovny.cz E-resources
- Keywords
- connective tissue disease‐associated interstitial lung disease, cryobiopsy, hypersensitivity pneumonitis, usual interstitial pneumonia,
- MeSH
- Biopsy methods MeSH
- Adult MeSH
- Idiopathic Pulmonary Fibrosis pathology complications diagnosis MeSH
- Lung Diseases, Interstitial * pathology diagnosis complications MeSH
- Middle Aged MeSH
- Humans MeSH
- Connective Tissue Diseases * complications pathology diagnosis MeSH
- Lung pathology MeSH
- Aged, 80 and over MeSH
- Aged MeSH
- Check Tag
- Adult MeSH
- Middle Aged MeSH
- Humans MeSH
- Male MeSH
- Aged, 80 and over MeSH
- Aged MeSH
- Female MeSH
- Publication type
- Journal Article MeSH
AIM: Transbronchial cryobiopsies are increasingly used for the diagnosis of interstitial lung disease (ILD), but there is a lack of published information on the features of specific ILD in cryobiopsies. Here we attempt to provide pathological guidelines for separating usual interstitial pneumonia (UIP) of idiopathic pulmonary fibrosis (IPF), fibrotic hypersensitivity pneumonitis (FHP) and connective tissue disease-associated ILD (CTD-ILD) in cryobiopsies. METHODS: We examined 120 cryobiopsies from patients with multidisciplinary discussion (MDD)-established CTD-ILD and compared them to a prior series of 121 biopsies from patients with MDD-established IPF or FHP. RESULTS: A non-specific interstitial pneumonia (NSIP) pattern alone was seen in 36 of 120 (30%) CTD-ILD, three of 83 (3.6%) FHP and two of 38 (5.2%) IPF cases, statistically favouring a diagnosis of CTD-ILD. The combination of NSIP + OP was present in 29 of 120 (24%) CTD-ILD, two of 83 (2.4%) FHP and none of 38 (0%) IPF cases, favouring a diagnosis of CTD-ILD. A UIP pattern, defined as fibroblast foci plus any of patchy old fibrosis/fibrosis with architectural distortion/honeycombing, was identified in 28 of 120 (23%) CTD-ILD, 45 of 83 (54%) FHP and 27 of 38 (71%) IPF cases and supported a diagnosis of FHP or IPF. The number of lymphoid aggregates/mm2 and fibroblast foci/mm2 was not different in IPF, CTD-ILD or FHP cases with a UIP pattern. Interstitial giant cells supported a diagnosis of FHP or CTD-ILD over IPF, but were infrequent. CONCLUSIONS: In the correct clinical/radiological context the pathological findings of NSIP, and particularly NSIP plus OP, favour a diagnosis of CTD-ILD in a cryobiopsy, but CTD-ILD with a UIP pattern, FHP with a UIP pattern and IPF generally cannot be distinguished.
Carolinas Pathology Group Atrium Health System Gainesville FL USA
Department of Laboratory Medicine and Pathology Mayo Clinic Phoenix AZ USA
Department of Medicine Division of Pulmonary Medicine Mayo Clinic Phoenix AZ USA
Department of Pathology Immunology and Laboratory Medicine University of Florida Gainesville FL USA
Department of Pathology St Paul's Hospital University of British Columbia Vancouver BC Canada
Division of Pulmonary Critical Care and Sleep Medicine University of Florida Gainesville FL USA
GB Morgagni Hospital and DIMEC University of Bologna Forli Bologna Forli Italy
See more in PubMed
Raghu G, Remy‐Jardin M, Myers JL et al. American Thoracic Society, European Respiratory Society, Japanese respiratory society, and Latin American Thoracic Society. Diagnosis of idiopathic pulmonary fibrosis. An official ATS/ERS/JRS/ALAT Clinical Practice Guideline. Am. J. Respir. Crit. Care Med. 2018; 198; e44–e68.
Raghu G, Remy‐Jardin M, Ryerson CJ et al. Diagnosis of hypersensitivity pneumonitis in adults. An official ATS/JRS/ALAT clinical practice guideline. Am. J. Respir. Crit. Care Med. 2020; 202; e36–e69.
Fernández Pérez ER, Travis WD, Lynch DA et al. Diagnosis and evaluation of hypersensitivity pneumonitis: CHEST guideline and expert panel report. Chest 2021; 160; e97–e156.
Cooper WA, Mahar A, Myers JL et al. Cryobiopsy for identification of usual interstitial pneumonia and other interstitial lung disease features. Further lessons from COLDICE, a prospective multicenter clinical trial. Am. J. Respir. Crit. Care Med. 2021; 203; 1306–1313.
Churg A, Tazelaar H, Matej R et al. Pathologic criteria for the diagnosis of usual interstitial pneumonia vs fibrotic hypersensitivity pneumonitis in transbronchial Cryobiopsies. Mod. Pathol. 2023; 36; 100221.
Monaghan H, Wells AU, Colby TV, du Bois RM, Hansell DM, Nicholson AG. Prognostic implications of histologic patterns in multiple surgical lung biopsies from patients with idiopathic interstitial pneumonias. Chest 2004; 125; 522–526.
Flaherty KR, Travis WD, Colby TV et al. Histopathologic variability in usual and nonspecific interstitial pneumonias. Am. J. Respir. Crit. Care Med. 2001; 164; 1722–1727.
Wahidi MM, Argento AC, Mahmood K et al. Comparison of forceps, cryoprobe, and thoracoscopic lung biopsy for the diagnosis of interstitial lung disease—the CHILL study. Respiration 2022; 101; 394–400.
Fortin M, Liberman M, Delage A et al. Transbronchial lung Cryobiopsy and SurgicAl LuNg biopsy: a prospective MultI‐CEntre agreement study (CAN‐ICE). Am. J. Respir. Crit. Care Med. 2023; 207; 1612–1619.
Romagnoli M, Colby TV, Berthet JP et al. Poor concordance between sequential transbronchial lung cryobiopsy and surgical lung biopsy in the diagnosis of diffuse interstitial lung diseases. Am. J. Respir. Crit. Care Med. 2019; 199; 1249–1256.
Zaizen Y, Tachibana Y, Ozasa M et al. Sensitivity of transbronchial lung cryobiopsy in the diagnosis of different interstitial lung diseases. Sci. Rep. 2022; 12; 22037.
Walsh SLF, Wells AU, Desai SR et al. Multicentre evaluation of multidisciplinary agreement on diagnosis in diffuse parenchymal lung disease: a case‐cohort study. Lancet Respir. Med. 2016; 4; 557–565.
Wright JL, Churg A, Hague CJ, Wong A, Ryerson CJ. Pathologic separation of idiopathic pulmonary fibrosis from fibrotic hypersensitivity pneumonitis. Mod. Pathol. 2020; 33; 616–625.
Smith ML, Hariri LP, Mino‐Kenudson M et al. Histopathologic assessment of suspected idiopathic pulmonary fibrosis: where we are and where we need to go. Arch. Pathol. Lab Med. 2020; 144; 1477–1489.
Sirol Aflah Syazatul S, Piciucchi S, Tomassetti S, Ravaglia C, Dubini A, Poletti V. Cryobiopsy in the diagnosis of bronchiolitis: a retrospective analysis of twenty‐three consecutive patients. Sci. Rep. 2020; 10; 10906.