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Hemophagocytic lymphohistiocytosis complicating a T-cell rich B-cell lymphoma
BACKGROUND: Hemophagocytic lymphohistiocytosis in adults is often secundary to an infection or a neoplasm. In this last case, T cell lymphomas are the most frequent causes. Hemophagocytic lymphohistiocytosis secundary to a B cell lymphoma has been rarely reported. CASE PRESENTATION: We describe a ca...
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| Vydáno v: | BMC Hematol |
|---|---|
| Hlavní autoři: | , , , , , , |
| Médium: | Artigo |
| Jazyk: | Inglês |
| Vydáno: |
BioMed Central
2016
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| Témata: | |
| On-line přístup: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5122011/ https://ncbi.nlm.nih.gov/pubmed/27904750 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s12878-016-0065-5 |
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