Bacillus Calmette–Guérin (BCG)‐associated hemophagocytic lymphohistiocytosis in the setting of IFN‐γR1 deficiency: A diagnostic dilemma

Hemophagocytic lymphohistiocytosis (HLH) disease is a severe immune dysregulation caused by mutations in genes required for lymphocyte cytotoxicity function. However, HLH‐like syndrome may develop secondary to infections, malignancy, and autoimmunity. Primary immunodeficiencies (PIDs) could predispo...

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Detalles Bibliográficos
Autores principales: Razaghian, Anahita, Parvaneh, Leila, Delkhah, Mona, Abbasi, Arash, Sadeghirad, Parisa, Shahrooei, Mohammad, Parvaneh, Nima
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2020
Materias:
Case Reports
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9175834/
https://www.ncbi.nlm.nih.gov/pubmed/35847695
http://dx.doi.org/10.1002/jha2.5

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9175834/
https://www.ncbi.nlm.nih.gov/pubmed/35847695
http://dx.doi.org/10.1002/jha2.5

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