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Hemophagocytic Lymphohistiocytosis Complicating Myelodysplasia

We describe a 62-year-old patient with a 4-year history of myelodysplasia who later developed striking features that included massive splenomegaly, rapidly evolving visual loss and a sensorimotor polyneuropathy. This led us to consider the diagnosis of haemophagocytic lymphohistiocytosis (HLH). Upon...

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Autors principals: Geraldine Quintero-Platt, Carima Belleyo-Belkasem, Taida Martín-Santos, Onán Pérez-Hernández, Emilio González-Reimers
Format: Artigo
Idioma:Inglês
Publicat: SMC MEDIA SRL 2014-03-01
Col·lecció:European Journal of Case Reports in Internal Medicine
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Accés en línia:http://ejcrim.com/index.php/EJCRIM/article/view/16
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