Sm. Lichtman et al., Secondary hemochromatosis as a long-term complication of the treatment of hematologic malignancies, AM J HEMAT, 61(4), 1999, pp. 262-264
The increased cure rate of hematologic malignancies including the use of bo
ne marrow transplantation has focused attention on the chronic toxicity and
quality of life of the survivors. We have observed five patients who have
been diagnosed with clinically significant iron overload, presumably due to
packed red blood cell transfusions, greater than or equal to 12 months aft
er transplant for a hematologic malignancy. In these patients, there is no
history of veno-occlusive disease or family history of hemochromatosis. The
allotransplant patient has been free of chronic graft versus host disease.
Family screening has been negative. No patient developed clinically signif
icant endocrinopathy, arthropathy, or cardiac disease. The patients have be
en treated with phlebotomy to bring the transferrin saturation and ferritin
levels to normal. The long-term follow-up of patients treated for a hemato
logic malignancy should include analysis of hepatitis C virus and iron stat
us. This may prevent the development of clinically significant chronic live
r disease and possibly malignancy. (C) 1999 Wiley-Liss, Inc.