HEMOCHROMATOSIS
- 1 January 1930
- journal article
- research article
- Published by American Medical Association (AMA) in Archives of internal medicine (1960)
- Vol. 45 (1) , 37-45
- https://doi.org/10.1001/archinte.1930.00140070044003
Abstract
In 1889, von Recklinghausen described a form of pigmentation affecting many organs of the body which he called hemochromatosis. This condition is often accompanied in its terminal stages by diabetes— the bronze diabetes of French writers. While the number of recorded cases (approximately a few over 100) would indicate that the condition is rare, various observers have pointed out that it may easily be overlooked clinically in the early stages when the skin pigmentation, glycosuria and the hemosiderin granules in the urine are absent. Mills1 reported that in seventeen pathologically advanced cases, only two were recognized during life and proved positive by the demonstration of hemosiderin in an excised piece of skin. Many patients, no doubt, die of intercurrent diseases before the positive clinical picture of hemochromatosis is established. Excellent pathologic and clinical studies are recorded in the literature. The characteristic pathologic picture is the presence of hemofuscin and hemosiderinThis publication has 1 reference indexed in Scilit:
- HEMOCHROMATOSIS AND CHRONIC POISONING WITH COPPERArchives of internal medicine (1960), 1926