A case report of idiopathic Hemophagocytic lymphohistiocytosis in an immunocompetent adult

Hemophagocytic lymphohistiocytosis poses a diagnostic dilemma due to the absence of specific clinical and laboratory findings, especially in adults. Despite greater recognition of the disease, secondary idiopathic forms are still reported.

Detalles Bibliográficos
Autores principales: Rabadão, Tiago, Naia, Leonor, Ferreira, Filipa, Teixeira, Mariana, Aveiro, Marcelo, Eulálio, Margarida, Silva, Fernando
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2021
Materias:
Case Reports
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8117811/
https://www.ncbi.nlm.nih.gov/pubmed/34026132
http://dx.doi.org/10.1002/ccr3.4006
Descripción
Sumario:Hemophagocytic lymphohistiocytosis poses a diagnostic dilemma due to the absence of specific clinical and laboratory findings, especially in adults. Despite greater recognition of the disease, secondary idiopathic forms are still reported.

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