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Initial management of paroxysmal nocturnal hemoglobinuria

Initial management of paroxysmal nocturnal hemoglobinuria
Diagnosis of PNH is based on absence or marked reduction of cell surface CD55/CD59 on two peripheral blood lineages by flow cytometry and FLAER. Refer to related UpToDate material for details of criteria for PNH diagnosis and severe BMF syndrome, PNH-associated clinical findings, supportive care, other aspects of PNH management, eligibility for allogeneic HCT, and management of BMF.
PNH: paroxysmal nocturnal hemoglobinuria; RBC: red blood cells; BMF: bone marrow failure; HCT: hematopoietic cell transplantation; ATG: anti-thymocyte globulin; FLAER: fluorescent aerolysin.
Graphic 131709 Version 3.0

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