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Waldenstrom macroglobulinaemia treated with sequential hemibody irradiation
Journal of Clinical Apheresis
|January 1, 1987
Summary
Waldenstrom macroglobulinaemia, a rare cancer, was treated effectively with plasmapheresis and irradiation. This approach managed symptoms and improved patient health, offering an alternative to chemotherapy.
Area of Science:
- Hematology
- Oncology
Background:
- Waldenstrom macroglobulinaemia is a rare lymphoproliferative disorder characterized by an IgM monoclonal gammopathy.
- Patients often present with symptoms of anemia, hyperviscosity, and lymphadenopathy.
Observation:
- A 40-year-old male presented with anemia and blurred vision, indicative of Waldenstrom macroglobulinaemia.
- Immediate symptom reversal was achieved with isovolaemic continuous-flow plasmapheresis and red cell transfusion.
Findings:
- Sequential hemibody irradiation was administered as specific therapy.
- At two-year follow-up, the patient exhibited excellent health with improved bone marrow hematopoietic reserve.
- Intermittent plasmapheresis was required to manage symptoms of rising blood viscosity.
Implications:
- Systemic irradiation is a well-tolerated palliative treatment for active macroglobulinaemia, reducing tumor burden.
- Irradiation offers an alternative to chemotherapy and may reduce, but not eliminate, the need for ongoing plasmapheresis.