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Bilateral renal vein thrombosis due to inapparent polycythaemia
Thromboses at unusual sites are characteristic of polycythaemia. We present a patient of bilateral renal vein thromboses due to polycythaemia that was inapparent. The diagnosis was confirmed by trilineage hyperplasia in bone marrow and JAK 2 V617F mutation in blood.
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Publicat a: | NDT Plus |
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Autors principals: | , , , , |
Format: | Artigo |
Idioma: | Inglês |
Publicat: |
Oxford University Press
2011
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Matèries: | |
Accés en línia: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4421442/ https://ncbi.nlm.nih.gov/pubmed/25949491 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/ndtplus/sfr047 |
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