Pulmonary Fibrosis in Children
| Autor: | Guillaume Thouvenin, Chiara Sileo, Hubert Ducou Le Pointe, Effrosyne Manali, Nadia Nathan, Aurore Coulomb L'Hermine, Annick Clement, Laura Berdah, Pierre-Louis Leger, Spyros Papiris, Céline Delestrain |
|---|---|
| Přispěvatelé: | Service de Pneumologie pédiatrique [CHU Trousseau], CHU Trousseau [APHP], Assistance publique - Hôpitaux de Paris (AP-HP) (AP-HP)-Sorbonne Université (SU)-Assistance publique - Hôpitaux de Paris (AP-HP) (AP-HP)-Sorbonne Université (SU), Physiopathologie des maladies génétiques d'expression pédiatrique (UMRS_933), Sorbonne Université (SU)-Institut National de la Santé et de la Recherche Médicale (INSERM), Assistance publique - Hôpitaux de Paris (AP-HP) (AP-HP)-Sorbonne Université (SU), National and Kapodistrian University of Athens (NKUA), Service de pathologie [CHU Trousseau], Maladies génétiques d'expression pédiatrique (U933), Institut National de la Santé et de la Recherche Médicale (INSERM)-CHU Trousseau [APHP], COST Action European network for translational research in children's and adult interstitial lung disease (COST-ILD) project CA16125Legs Poix from the Chancellerie des Universites, Paris 1305, 1405, 1015, 2077, DP2017/1860European Commission 305653Respirer c'est GrandirBelleherbe Association, ANR-10-COHO-0003,RADICO,Cohorte nationale maladies rares(2010), European Project: 305653,EC:FP7:HEALTH,FP7-HEALTH-2012-INNOVATION-1,CHILD-EU(2012) |
| Jazyk: | angličtina |
| Rok vydání: | 2019 |
| Předmět: |
Pediatrics
medicine.medical_specialty lcsh:Medicine Review [SDV.MHEP.PSR]Life Sciences [q-bio]/Human health and pathology/Pulmonology and respiratory tract nonspecific interstitial pneumonia 03 medical and health sciences 0302 clinical medicine children Usual interstitial pneumonia Pulmonary fibrosis medicine usual interstitial pneumonia 030304 developmental biology interstitial lung disease 0303 health sciences [SDV.MHEP.PED]Life Sciences [q-bio]/Human health and pathology/Pediatrics Adult patients pulmonary fibrosis business.industry lcsh:R Interstitial lung disease General Medicine medicine.disease Pathophysiology 3. Good health 030228 respiratory system business |
| Zdroj: | Journal of Clinical Medicine Journal of Clinical Medicine, MDPI, 2019, 8 (9), pp.1312. ⟨10.3390/jcm8091312⟩ Journal of Clinical Medicine, Vol 8, Iss 9, p 1312 (2019) Journal of Clinical Medicine, 2019, 8 (9), pp.1312. ⟨10.3390/jcm8091312⟩ |
| ISSN: | 2077-0383 |
| DOI: | 10.3390/jcm8091312⟩ |
| Popis: | International audience; Pulmonary fibrosis (PF) is a very rare condition in children, which may be observed in specific forms of interstitial lung disease. None of the clinical, radiological, or histological descriptions used for PF diagnosis in adult patients, especially in situations of idiopathic PF, can apply to pediatric situations. This observation supports the view that PF expression may differ with age and, most likely, may cover distinct entities. The present review aims at summarizing the current understanding of PF pathophysiology in children and identifying suitable diagnostic criteria. View Full-Text |
| Databáze: | OpenAIRE |
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