Paediatric sarcoidosis.

Autor: Nathan N; Service de Pneumologie Pédiatrique et Centre de référence des maladies respiratoires rares, AP-HP, Hôpital Trousseau, Unité INSERM UMR-S933, Sorbonne Université, Paris, France. Electronic address: nadia.nathan@aphp.fr., Sileo C; Service de Radiologie Pédiatrique, AP-HP, Hôpital Trousseau, Paris, France. Electronic address: chiara.sileo@aphp.fr., Calender A; Service de Génétique, CHU Lyon, Equipe EA7426 (PI3) Inflammation et immunité de l'épithélium respiratoire, Lyon, France. Electronic address: alain.calender@chu-lyon.fr., Pacheco Y; Service de Génétique, CHU Lyon, Equipe EA7426 (PI3) Inflammation et immunité de l'épithélium respiratoire, Lyon, France. Electronic address: yves.pacheco@univ-lyon1.fr., Rosental PA; SLICOSIS Groupe, European Research Council (ERC)/SILICOSIS project, Centre for European Studies and Comparative Politics, Sciences Po, Paris, France. Electronic address: paulandre.rosental@sciencespo.fr., Cavalin C; SLICOSIS Groupe, European Research Council (ERC)/SILICOSIS project, Centre for European Studies and Comparative Politics, Sciences Po, Paris, France. Electronic address: catherine.cavalin@sciencespo.fr., Macchi O; SLICOSIS Groupe, European Research Council (ERC)/SILICOSIS project, Centre for European Studies and Comparative Politics, Sciences Po, Paris, France. Electronic address: odile.macchi@sciencespo.fr., Valeyre D; AP-HP Service de pneumologie, Hôpital Avicenne, EA2363, Université Paris 13, Bobigny, France. Electronic address: dominique.valeyre@aphp.fr., Clement A; Service de Pneumologie Pédiatrique et Centre de référence des maladies respiratoires rares, AP-HP, Hôpital Trousseau, Unité INSERM UMR-S933, Sorbonne Université, Paris, France. Electronic address: annick.clement@aphp.fr.
Jazyk: angličtina
Zdroj: Paediatric respiratory reviews [Paediatr Respir Rev] 2019 Feb; Vol. 29, pp. 53-59. Date of Electronic Publication: 2018 May 19.
DOI: 10.1016/j.prrv.2018.05.003
Abstrakt: Paediatric sarcoidosis is an extremely rare disease characterized by a granulomatous inflammation. The estimated incidence is 0.6-1.02/100,000 children, but in the absence of international registers, the disease is probably under-reported. Its pathophysiologic basis is not clearly understood but the current hypothesis is a combination of a genetic predisposition and an environmental exposure that could be either organic or mineral. Contrary to adult forms of the disease, general symptoms are often at the forefront at diagnosis. In its most frequent form, paediatric sarcoidosis is a multi-organ disorder affecting preferentially the lungs, the lymphatic system and the liver, but all organs can be affected. This review aims to provide an overview of current knowledge on sarcoidosis in children, providing a summary of the data available from cohort studies on the presentation, the management and the evolution of the disease in this specific population.
(Copyright © 2018 Elsevier Ltd. All rights reserved.)
Databáze: MEDLINE
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