| Autor: |
Izaskun Rubio Ollo, Mercedes Regulez Uranga, Cristina Prieto Valtuille, Raquel Pérez Garay, A. López-Urrutia Fernández, Begoña Basauri Elorza |
| Rok vydání: |
2008 |
| Předmět: |
|
| Zdroj: |
Revista del Laboratorio Clínico. 1:68-70 |
| ISSN: |
1888-4008 |
| DOI: |
10.1016/j.labcli.2008.06.001 |
| Popis: |
Hemophagocytic syndrome or hemophagocytic lymphohistiocytosis is a severe, rare and possibly mis-diagnosed syndrome. It is characterized by an exaggerated inflammatory response due to the activation of macrophages and T lymphocytes, and diagnosis and treatment is needed as soon as possible. We present the case of a 61 year old male patient with a rapid and fatal progression and rarely decribed Ferritin's levels. |
| Databáze: |
OpenAIRE |
| Externí odkaz: |
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