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Objective Response in Amyloidosis Treated With Intermittent Chemotherapy
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1984
Year
Light Chain ImmunoglobulinAutoimmune DiseaseImmunologyPathologyPharmacotherapyDestructive Bony LesionsMetronomic ChemotherapyNeuropathologyMedicineObjective ResponseTreatment37-Year-old Woman
A 37-year-old woman with amyloidosis derived from light chain immunoglobulin had hepatosplenomegaly, elevated serum alkaline phosphatase values, and progressively destructive bony lesions. A 44-month intermittent course of chemotherapy with melphalan and prednisone resulted in regression, confirming the occasional efficacy of cytotoxic chemotherapy in this disease.