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This case report discusses a patient with multiple myeloma (MM) who experienced severe bleeding due to acquired hemophilia A and acquired von Willebrand syndrome, alongside hyperactivation of factor IX. Despite initial treatment improving bleeding tendencies, the patient developed central retinal vein occlusion, indicating a risk for thromboembolic complications. Ultimately, all coagulation abnormalities resolved following successful treatment of MM with allogeneic hematopoietic stem cell transplantation, h

Author

layla

Language

EN