Carmen Benet Campos

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| 1422 | haematologica | 2008; 93(9) ment options. We observed that those of our patients treated with rituximab-based regimens who were assigned to the high risk group had a median overall and cause-specific survival of less than four years. When such patients were treated with alkylating agents or with nucleoside analogs median overall survival was also(More)
BACKGROUND Hereditary Hyperferritinaemia Cataract Syndrome (HHCS) is a rare autosomal dominant disease characterized by increased serum ferritin levels and early onset of bilateral cataract. The disease is caused by mutations in the Iron-Responsive Element (IRE) located in the 5' untranslated region of L-Ferritin (FTL) mRNA, which post-transcriptionally(More)
A 60-year-old man was admitted because of fever and dyspnea. He was diagnosed with deep vein thrombosis (DVT) and pulmonary embolism. His blood count showed leukocytosis (47.43 10/L) and eosinophilia (33.23 10/L) without other cytopenias. A blood smear revealed atypical eosinophils; these had large and degranulated cytoplasms with hyperlobulated nuclei.(More)
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