Long term follow-up of pediatric-onset Evans syndrome: broad immunopathological manifestations and high treatment burden

Pediatric-onset Evans syndrome (pES) is defined by both immune thrombocytopenic purpura (ITP) and autoimmune hemolytic anemia (AIHA) before the age of 18 years. There have been no comprehensive long-term studies of this rare disease, which can be associated to various immunopathological manifestatio...

Descripción completa

Detalles Bibliográficos
Autores principales: Pincez, Thomas, Fernandes, Helder, Leblanc, Thierry, Michel, Gérard, Barlogis, Vincent, Bertrand, Yves, Neven, Bénédicte, Chahla, Wadih Abou, Pasquet, Marlène, Guitton, Corinne, Marie-Cardine, Aude, Pellier, Isabelle, Armari-Alla, Corinne, Benadiba, Joy, Blouin, Pascale, Jeziorski, Eric, Millot, Frédéric, Paillard, Catherine, Thomas, Caroline, Cheikh, Nathalie, Bayart, Sophie, Fouyssac, Fanny, Piguet, Christophe, Deparis, Marianna, Briandet, Claire, Doré, Eric, Picard, Capucine, Rieux-Laucat, Frédéric, Landman-Parker, Judith, Leverger, Guy, Aladjidi, Nathalie
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Fondazione Ferrata Storti 2021
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8804581/
https://www.ncbi.nlm.nih.gov/pubmed/33440924
http://dx.doi.org/10.3324/haematol.2020.271106

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8804581/
https://www.ncbi.nlm.nih.gov/pubmed/33440924
http://dx.doi.org/10.3324/haematol.2020.271106

Ejemplares similares