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.

Detalles Bibliográficos
Autores principales: Rapur, Ram, Gudithi, Swarnalatha, Adiraju, Krishna Prasad, Vangipurapu Rangacharlu, Srinivasasan, Venkata, Dakshinamurty Kaligotla
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2011
Materias:
II. Clinical Reports
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4421442/
https://www.ncbi.nlm.nih.gov/pubmed/25949491
http://dx.doi.org/10.1093/ndtplus/sfr047
Descripción
Sumario: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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