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...

Full description

Bibliographic Details
Main Authors: Geraldine Quintero-Platt, Carima Belleyo-Belkasem, Taida Martín-Santos, Onán Pérez-Hernández, Emilio González-Reimers
Format: Article
Language:English
Published: SMC MEDIA SRL 2014-03-01
Series:European Journal of Case Reports in Internal Medicine
Subjects:
Online Access:http://ejcrim.com/index.php/EJCRIM/article/view/16