Hemophagocytic inflammatory syndrome in ADA-SCID: report of two cases and literature review

Hemophagocytic inflammatory syndrome (HIS) is a rare form of secondary hemophagocytic lymphohistiocytosis caused by an impaired equilibrium between natural killer and cytotoxic T-cell activity, evolving in hypercytokinemia and multiorgan failure. In the context of inborn errors of immunity, HIS occu...

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Detalles Bibliográficos
Autores principales: Fratini, Elena Sophia, Migliavacca, Maddalena, Barzaghi, Federica, Fossati, Claudia, Giannelli, Stefania, Monti, Ilaria, Casiraghi, Miriam, Ferrua, Francesca, Recupero, Salvatore, Consiglieri, Giulia, Calbi, Valeria, Tucci, Francesca, Gallo, Vera, Bernardo, Maria Ester, Cenciarelli, Sabina, Palmoni, Monica, Moni, Margherita, Galimberti, Luca, Duse, Marzia, Leonardi, Lucia, Sieni, Elena, Soncini, Elena, Porta, Fulvio, Notarangelo, Lucia Dora, De Santis, Raffaella, Ladogana, Saverio, Aiuti, Alessandro, Cicalese, Maria Pia
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2023
Materias:
Immunology
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10331599/
https://www.ncbi.nlm.nih.gov/pubmed/37435083
http://dx.doi.org/10.3389/fimmu.2023.1187959

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10331599/
https://www.ncbi.nlm.nih.gov/pubmed/37435083
http://dx.doi.org/10.3389/fimmu.2023.1187959

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