Management of paroxysmal nocturnal hemoglobinuria in CALR mutated post‐essential thrombocythemia myelofibrosis: A case report

Abstract Paroxysmal nocturnal hemoglobinuria (PNH) results from the loss of erythrocyte surface proteins, leading to complement activation and its spectrum of effects. We explore this case of a 57‐year‐old man with post‐essential thrombocythemia (ET) myelofibrosis (MF) who developed symptomatic anem...

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Bibliographic Details
Published in:eJHaem
Main Authors: Mahija Cheekati, KarLeung Siu, Rachel Ochs
Format: Article
Language:English
Published: Wiley 2024-04-01
Subjects:
CALR
case report
myelofibrosis
PNH
thrombocythemia
Online Access:https://doi.org/10.1002/jha2.892

Internet

https://doi.org/10.1002/jha2.892

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