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Hemophagocytic lymphohistiocytosis complicated by polyserositis: A case report
BACKGROUND: Hemophagocytic lymphohistiocytosis (HLH) is a rare group of disorders of immune dysregulation characterized by clinical symptoms of severe inflammation. There are basically two types of clinical scenarios: Familial HLH and sporadic HLH. It is thought that the syndrome is implicated in th...
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| Publicado no: | World J Clin Cases |
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| Main Authors: | , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Baishideng Publishing Group Inc
2019
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6795728/ https://ncbi.nlm.nih.gov/pubmed/31624756 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.12998/wjcc.v7.i19.3069 |
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