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Management of paroxysmal nocturnal hemoglobinuria

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.
ATG: anti-thymocyte globulin; BMF: bone marrow failure; FLAER: fluorescent aerolysin; HCT: hematopoietic cell transplantation; PNH: paroxysmal nocturnal hemoglobinuria; RBC: red blood cells.
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