Unusual case of adult hemophagocytic syndrome

Hemophagocytic syndrome (HPS) is an uncommon manifestation in systemic lupus erythematosus (SLE). Clinical features of HPS include fever, pancytopenia, abnormal liver enzyme, hepatosplenomegaly, lymphadenopathy, and coagulation disorder. HPS comprises primary and reactive forms. Herein, we describe...

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Detalles Bibliográficos
Autores principales: Tamizifar, Babak, Samadi, Golnaz, Rismankarzadeh, Maryam
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Medknow Publications & Media Pvt Ltd 2014
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3999605/
https://www.ncbi.nlm.nih.gov/pubmed/24778673

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3999605/
https://www.ncbi.nlm.nih.gov/pubmed/24778673

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