Fibrosierte Hypersensitivitätspneumonie: Fokus auf pathologierelevante Aspekte der neuen klinischen Leitlinie der ATS/JRS/ALAT zur Diagnostik der Hypersensitivitätspneumonie bei Erwachsenen [Fibrotic hypersensitivity pneumonia: focus on pathology-relevant aspects of the new ATS/JRS/ALAT clinical guideline for the diagnosis of hypersensitivity pneumonia in adults]

Détails

Ressource 1Télécharger: Berezowska2021_Article_FibrosierteHypersensitivitätsp.pdf (2187.21 [Ko])
Etat: Public
Version: Final published version
Licence: CC BY 4.0
ID Serval
serval:BIB_B26A4D252A71
Type
Article: article d'un périodique ou d'un magazine.
Sous-type
Synthèse (review): revue aussi complète que possible des connaissances sur un sujet, rédigée à partir de l'analyse exhaustive des travaux publiés.
Collection
Publications
Institution
Titre
Fibrosierte Hypersensitivitätspneumonie: Fokus auf pathologierelevante Aspekte der neuen klinischen Leitlinie der ATS/JRS/ALAT zur Diagnostik der Hypersensitivitätspneumonie bei Erwachsenen [Fibrotic hypersensitivity pneumonia: focus on pathology-relevant aspects of the new ATS/JRS/ALAT clinical guideline for the diagnosis of hypersensitivity pneumonia in adults]
Périodique
Der Pathologe
Auteur(s)
Berezowska S.
ISSN
1432-1963 (Electronic)
ISSN-L
0172-8113
Statut éditorial
Publié
Date de publication
02/2021
Peer-reviewed
Oui
Volume
42
Numéro
1
Pages
48-54
Langue
allemand
Notes
Publication types: Journal Article ; Review
Publication Status: ppublish
Résumé
Hypersensitivity pneumonia (HP), also called exogenous allergic alveolitis, is a chronic interstitial pneumonia induced by a hypersensitivity reaction to an identified or unidentified antigen in exposed and susceptible individuals that may progress to terminal lung fibrosis. The diagnosis of HP presents a diagnostic challenge. Though therapeutically important, it may be particularly difficult to differentiate fibrotic HP, historically termed chronic HP, from idiopathic pulmonary fibrosis (IPF) or interstitial lung disease associated with connective tissue diseases (CTD-ILD). Multidisciplinary discussion and thus a synoptic evaluation of all findings is firmly established as the gold standard diagnostic approach in interstitial lung diseases including HP. Nonetheless, the high interobserver variability between experts from the individual disciplines (pulmonology, radiology, and pathology) and between experienced multidisciplinary teams in assessing the diagnostic probability of HP has highlighted the need for widely accepted guidelines.The present review summarizes pathology-relevant aspects of the new ATS/JRS/ALAT clinical practice guideline for the diagnosis of HP in adults.
Mots-clé
Adult, Alveolitis, Extrinsic Allergic/diagnosis, Humans, Idiopathic Pulmonary Fibrosis/diagnosis, Lung, Lung Diseases, Interstitial/diagnosis, Pneumonia, Radiography, Chronic fibrotic lung disease, Exogenous allergic alveolitis, Granuloma, Hypersensitivity pneumonitis, Idiopathic interstitial Pneumonia
Pubmed
Web of science
Open Access
Oui
Création de la notice
29/12/2020 13:17
Dernière modification de la notice
02/03/2021 6:25
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