[Acute chest syndrome in adult sickle cell patients].
Syndrome thoracique aigu chez les patients drépanocytaires adultes.
Acute chest syndrome
Blood transfusion
Drépanocytose
Hémoglobine S
Incentive spirometry
S hemoglobin
Sickle cell disease
Spirométrie incitative
Syndrome thoracique aigu
Transfusion
Journal
La Revue de medecine interne
ISSN: 1768-3122
Titre abrégé: Rev Med Interne
Pays: France
ID NLM: 8101383
Informations de publication
Date de publication:
Aug 2022
Aug 2022
Historique:
received:
02
01
2022
revised:
26
03
2022
accepted:
09
04
2022
pubmed:
10
7
2022
medline:
4
8
2022
entrez:
9
7
2022
Statut:
ppublish
Résumé
Sickle cell disease is a frequent genetic condition, due to a mutation of the β-globin gene, leading to the production of an abnormal S hemoglobin and characterized by multiple vaso-occlusive events. The acute chest syndrome is a severe complication associated with a significant disability and mortality. It is defined by the association of one or more clinical respiratory manifestations and a new infiltrate on lung imaging. Its pathophysiology is complex and implies vaso-occlusive phenomena (pulmonary vascular thrombosis, fat embolism), infection, and alveolar hypoventilation. S/S or S/β
Identifiants
pubmed: 35810055
pii: S0248-8663(22)00440-4
doi: 10.1016/j.revmed.2022.04.019
pii:
doi:
Substances chimiques
Hemoglobins
0
Types de publication
Journal Article
Langues
fre
Sous-ensembles de citation
IM
Pagination
470-478Informations de copyright
Copyright © 2022 Société Nationale Française de Médecine Interne (SNFMI). Published by Elsevier Masson SAS. All rights reserved.