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A Case of Hemophagocytic Lymphohistiocytosis Secondary to Disseminated Histoplasmosis
Hemophagocytic lymphohistiocytosis (HLH) is a rare condition characterized by a pathologic immune dysregulation resulting in extreme inflammation. Clinical manifestations are varied but can include severe multiorgan failure and death. HLH has been associated with malignancies, autoimmune diseases, a...
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| Publicado no: | Case Reports Hepatol |
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| Main Authors: | , , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Hindawi
2020
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7455843/ https://ncbi.nlm.nih.gov/pubmed/32884850 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1155/2020/6901514 |
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