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S. Finch, C. Finch (1955)
IDIOPATHIC HEMOCHROMATOSIS, AN IRON STORAGE DISEASE: A. Iron Metabolism in HemochromatosisMedicine, 34
G. Jacobson, S. Zucherman (1956)
Roentgenographically demonstrable splenic deposits in sickle cell anemia.The American journal of roentgenology, radium therapy, and nuclear medicine, 76 1
S. Schwartz (1956)
Exogenous hemochromatosis; concept and general description.American journal of clinical pathology, 26 7
J. Small, R. Lillie (1954)
Histopathologic Technic and Practical Histochemistry
Approximately 80 cases of exogenous hemosiderosis have been reported in the literature since 1948. This entity has been termed by various observers as iron overload, transfusional hemosiderosis, and secondary hemochromatosis.1 In a review of the literature on hemochromatosis and hemosiderosis we found few references to the x-ray findings in these conditions. Increased liver density, found by use of x-rays, has been reported in cases of hemochromatosis.2 Increased density of the spleen, however, has not been referred to previously. The occurrence of iron and calcium deposits in the spleen in patients with sickle cell anemia has previously been described.3 In idiopathic hemosiderosis, the iron is stored predominantly in the liver; in exogenous hemochromatosis, a greater amount of iron appears to be concentrated in the spleen.4 We were therefore not surprised that in some patients with transfusional hemosiderosis an increased density of the spleen could be seen on
JAMA – American Medical Association
Published: Sep 6, 1958
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