Haemosiderosis and haemochromatosis of synovial tissues.
نویسنده
چکیده
منابع مشابه
Transfusional Haemosiderosis Simulating
Haemochromatosis is a disease occurring predominantly in men, and characterized by excessive deposition of iron in the tissues, coexisting with skin pigmentation and hepatic, pancreatic, and testicular fibrosis. The condition is described by Sheldon (1935) in whose monograph 311 cases are reviewed. Parenteral iron given in excess of requirements will be deposited in the tissues, since, with the...
متن کاملA case of paroxysmal nocturnal haemoglobinuria associated with secondary haemochromatosis, a lower nephron nephrosis, and a megaloblastic anaemia.
Secondary or exogenous haemochromatosis has been defined by Aufderheide, Horns, and Goldish (1953) as a condition acquired as " a consequence of anaemia, blood transfusion, or both, and characterized by increased hepatic and total body iron and unequivocal portal cirrhosis." These authors found only 20 cases in the literature and has-e added two more of their own. They comment on the lack of ad...
متن کاملA pathological study of idiopathic haemochromatosis and its relationship to siderosis in liver cirrhosis.
HAEMOCHROMATOSIS refers to a general increase in body iron stores with tissue damage. The pathological criteria used for the diagnosis of haemochromatosis were those proposed by MacDonald and Mallory (1960). They were as follows: 1. Cirrhosis of the liver of a "portal type". 2. Excessive iron deposits in hepatic parenchymal cells, in connective tissue, and in bile duct epithelium. 3. Pancreatic...
متن کاملAlterations in tissue ferritins in iron storage disorders.
Purified tissue ferritins isolated from Bantu subjects with gross haemosiderosis, from a patient with idiopathic haemochromatosis (HC) treated by phlebotomy, and from rats with experimental iron overload were studied in order to determine the significance of the abnormality previously demonstrated in tissue isoferritins in patients with IHC. The isoferrin profile of the tissues from the Bantu s...
متن کامل[Haemosiderosis bulbi in a patient with myelodysplastic syndrome (MDS RAEB-1)].
Haemosiderosis bulbi is a degenerative condition of the eye bulb caused by the toxic effects of an intracellular accumulation of haemosiderin. Haemosiderin is a product of the decomposition of haemoglobin. The most common and severe damage takes place in the epithelial cells of the eye tissues. Haemosiderosis bulbi is a complication of the long existing haemophthalmus, the intravitreal bleeding...
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عنوان ژورنال:
- The Journal of bone and joint surgery. British volume
دوره 33-B 3 شماره
صفحات -
تاریخ انتشار 1951