Cargando…
Hemophagocytic lymphohistiocytosis presented with fever of unknown origin: A case study and literature review
Hemophagocytic lymphohistiocytosis (HLH) is a rare and life‐threatening clinical syndrome, which may present with FUO. The possible diagnosis of HLH must be considered in the differential diagnosis when a patient presents with FUO.
Autores principales: | Hakamifard, Atousa, Mardani, Masoud, Gholipur‐Shahraki, Tahereh |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2021
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8077318/ https://www.ncbi.nlm.nih.gov/pubmed/33936693 http://dx.doi.org/10.1002/ccr3.4033 |
Ejemplares similares
-
Bendamustine and pneumocystis pneumonia: A systematic review
por: Hakamifard, Atousa, et al.
Publicado: (2022) -
Hemophagocytic lymphohistiocytosis (HLH) presenting as fever of unknown origin and acute liver failure
por: Lutfi, Forat, et al.
Publicado: (2018) -
Hemophagocytic Lymphohistiocytosis (HLH) Associated with T-Cell Lymphomas: Broadening our Differential for Fever of Unknown Origin
por: Khadanga, Sherrie, et al.
Publicado: (2014) -
Hemophagocytic lymphohistiocytosis as a diagnostic consideration of fever of unknown origin with pancytopenia and chronic liver disease
por: Amisha,, et al.
Publicado: (2019) -
Sepsis of unknown origin with multiorgan failure syndrome: Think of hemophagocytic lymphohistiocytosis
por: Maheshwari, Namrata, et al.
Publicado: (2015)