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Hemophagocytic lymphohistiocytosis associated to Haemophilus parainfluenzae endocarditis- a case report.
- Source :
- Acta Clinica Belgica (English ed. Printed)
- Publication Year :
- 2017
-
Abstract
- Hemophagocytic lymphohistiocytosis (HLH) is a rare but severe and potentially fatal syndrome that is characterized by increased proliferation and activation of benign macrophages with hemophagocytosis throughout the reticuloendothelial system. This syndrome is classified as primary (genetic) or secondary when acquired in the context of infections (usually viral), malignancies, rheumatologic and metabolic diseases.<br />SCOPUS: ar.j<br />info:eu-repo/semantics/published
Details
- Database :
- OAIster
- Journal :
- Acta Clinica Belgica (English ed. Printed)
- Notes :
- No full-text files, English
- Publication Type :
- Electronic Resource
- Accession number :
- edsoai.on1029465140
- Document Type :
- Electronic Resource