Secondary Hemochromatosis

Author:

AUFDERHEIDE ARTHUR C.1,HORNS HOWARD L.1,GOLDISH ROBERT J.1

Affiliation:

1. Departments of Pathology and Medicine, Veterans Administration Hospital and University of Minnesota Medical School, Minneapolis, Minn.

Abstract

Abstract 1. Secondary hemochromatosis has been sharply separated from simple hemosiderosis by defining the former as "a condition acquired as a consequence of anemia, blood transfusions, or both, and characterized by increased hepatic and total body iron content and unequivocal portal cirrhosis of the liver." 2. Previously reported cases are critically reviewed in the light of this definition. 3. Two new cases of secondary (exogenous) hemochromatosis are reported. 4. Anemia is postulated as the basic etiologic factor in secondary hemochromatosis by causing increased iron absorption; iron introduced in the form of blood transfusions probably only accelerates a process already in progress. 5. Prolonged futile oral iron therapy may be harmful. 6. A plea is made for a strict concept of secondary hemochromatosis as well as for thorough documentation of future reports.

Publisher

American Society of Hematology

Subject

Cell Biology,Hematology,Immunology,Biochemistry

Cited by 45 articles. 订阅此论文施引文献 订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献

1. Anémie primitive réfractaire avec hypersidérose sanguine médullaire et hépatique - (cas féminin);Acta Medica Scandinavica;2009-04-24

2. Iron Overload;Iron Metabolism;1983

3. Iron;Trace Elements and Iron in Human Metabolism;1978

4. The effect of maternal partial exchange transfusion on the infants of patients with sickle cell anemia;The Journal of Pediatrics;1976-08

5. Iron in the heart;The American Journal of Medicine;1971-08

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