| Literature DB >> 29359139 |
Madhura Hanmantgad1, Rajat Nog1,2, Karen Seiter1,2.
Abstract
Eculizumab has become the standard of care for patients with paroxysmal nocturnal hemoglobinuria (PNH). As more patients are treated, the long-term outcomes of these patients will become apparent. We recently treated a patient who developed PNH in the setting of aplastic anemia. The patient developed acute myeloid leukemia less than three years after initiating eculizumab. The patient also died suddenly from Scedosporium sepsis during induction therapy. This patient's course seemed more aggressive than would be expected. The possible effect of complement blockade is discussed.Entities:
Keywords: Eculizumab; Scedosporium; acute; hemoglobinuria; leukemia; myeloid; paroxysmal
Year: 2017 PMID: 29359139 PMCID: PMC5763031 DOI: 10.21037/sci.2017.12.04
Source DB: PubMed Journal: Stem Cell Investig ISSN: 2306-9759