ACUTE HEMOLYTIC ANEMIA AND HEMOGLOBINURIA FOLLOWING SULFADIAZINE MEDICATION
نویسندگان
چکیده
منابع مشابه
Chronic Acquired Hemolytic Anemia Associated with Hemoglobinuria and Raynaud’s Phenomena
idiopathic acquired hemolytic atsemia, Group II, hemolytic atsemia followitsg irus pmseumomsia and Group III, chrotsic hemolytic atsemia with hemoglohitsuria and Raynaud’s phemsomena. A detailed accoumst. of the climsical aspects of tise three patients of Group III was published by Ferrimams, Dacie, Keele amid Fullerton2 who also made an amsalysis of msine similar cases reported in the literatu...
متن کاملChronic acquired hemolytic anemia associated with hemoglobinuria and Raynaud's phenomena.
idiopathic acquired hemolytic atsemia, Group II, hemolytic atsemia followitsg irus pmseumomsia and Group III, chrotsic hemolytic atsemia with hemoglohitsuria and Raynaud’s phemsomena. A detailed accoumst. of the climsical aspects of tise three patients of Group III was published by Ferrimams, Dacie, Keele amid Fullerton2 who also made an amsalysis of msine similar cases reported in the literatu...
متن کاملAutohemagglutinins and hemolysins with hemoglobinuria and acute hemolytic anemia, in an illness resembling infectious mononucleosis.
CUTE acquired hemolytic anemia is uncommon, but dramatic in its clinical picture and often disastrous in its outcome. In 1940, Dameshek and Schwartz’ assembled about ioo cases reported in the literature since 1907, in which no definite etiology was evident. In addition, as cited by these authors, cases have been reported in which the anemia developed in association with definite or probable eti...
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A 43-year-old African-American man with a history of hypertension, depression, and chronic alcohol abuse presented to the emergency service of an outside hospital complaining of chest pain. Laboratory testing indicated hepatocellular injury with aspartate aminotransferase (AST) of 14000 U/L (reference interval 5– 41 U/L) and alanine aminotransferase (ALT) of 6400 U/L (reference interval 8 – 45 ...
متن کاملAutoimmune hemolytic anemias and paroxysmal nocturnal hemoglobinuria
The hallmark of the autoimmune hemolytic anemias (AIHAs) and paroxysmal nocturnal hemoglobinuria (PNH) is shortened red blood cell survival. Although AIHA and PNH share the critical feature of shortened red cell survival, the mechanisms underlying this characteristic differ significantly between the two diseases. In the case of AIHA, autoantibodies directed against the patient’s own red blood c...
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ژورنال
عنوان ژورنال: Blood
سال: 1946
ISSN: 0006-4971,1528-0020
DOI: 10.1182/blood.v1.3.189.189