Adult chronic rhinosinusitis

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作者
Claus Bachert
Bradley Marple
Rodney J. Schlosser
Claire Hopkins
Robert P. Schleimer
Bart N. Lambrecht
Barbara M. Bröker
Tanya Laidlaw
Woo-Jung Song
机构
[1] Sun Yat-sen University,Upper Airways Research Laboratory
[2] International Airway Research Center,Division of ENT diseases, CLINTEC, Karolinska Institute
[3] First Affiliated Hospital,ENT Department
[4] Ghent University,Division of Allergy and Immunology, Department of Medicine
[5] University of Stockholm,Department of Internal Medicine and Pediatrics
[6] University of Texas,Department of Pulmonary Medicine
[7] Southwestern Medical Center,Department of Immunology, Institute of Immunology and Transfusion Medicine
[8] Department of Otolaryngology – Head and Neck Surgery,Department of Medicine, Harvard Medical School, the Division of Allergy and Clinical Immunology
[9] Medical University of South Carolina,Department of Allergy and Clinical Immunology, Asan Medical Center
[10] Department of Otolaryngology – Head and Neck Surgery,undefined
[11] Guy’s Hospital,undefined
[12] Northwestern University Feinberg School of Medicine,undefined
[13] Laboratory of Immunoregulation,undefined
[14] VIB-UGhent Center for Inflammation Research,undefined
[15] Ghent University,undefined
[16] ErasmusMC,undefined
[17] University Medicine Greifswald,undefined
[18] Brigham and Women’s Hospital,undefined
[19] University of Ulsan College of Medicine,undefined
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摘要
Chronic rhinosinusitis (CRS) occurs in >10% of the adult population in Europe and the USA and can be differentiated into CRS without nasal polyps and CRS with nasal polyps (CRSwNP). Both phenotypes are characterized by a high disease burden and an overlapping spectrum of symptoms, with facial pain and loss of smell being the most differentiating. Great progress has been made in the understanding of CRS pathophysiology: from the epithelium and epithelial–mesenchymal transition to innate and adaptive immunity pathways and, finally, on the role of eosinophils and Staphylococcus aureus in the persistence of disease. Although clinical manifestations and diagnostic tools (including nasal endoscopy and imaging) have undergone major changes over the past few years, management (including pharmacotherapy, surgery and biologics) has experienced enormous progress based on the growing knowledge of key mediators in severe CRSwNP. The introduction of endotyping has led to a differentiation of ‘tailored’ surgical approaches, focusing on the mucosal concept in those with severe CRSwNP and on the identification of patients eligible for extended surgery and possibly biologics in the future.
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