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Dtsch Med Wochenschr ; 119(42): 1421-6, 1994 Oct 21.
Artigo em Alemão | MEDLINE | ID: mdl-7956758

RESUMO

An 18-year-old woman developed an acute haemolytic anaemia, acute transient renal failure and progressive hepatic failure. Coeruloplasmin and serum copper concentration were normal; a Kayser-Fleischer ring and any neurological symptoms were absent initially. Liver biopsy was contraindicated because of increased bleeding tendency. Wilson's disease was diagnosed only after the acute renal failure had regressed, on the basis of the urinary copper excretion (2890 micrograms/d, rising to 7330 micrograms/d after D-penicillamine administration). Progressive liver failure required transplantation. After it the patient quickly recovered and is now, two years later, free of disease. -This case demonstrates that Wilson's disease may be difficult to diagnose at the time of initial acute manifestation. But it can be recognized early from the pathognomonic low alkaline phosphatase and by calculation of free serum copper.


Assuntos
Anemia Hemolítica/diagnóstico , Degeneração Hepatolenticular/diagnóstico , Falência Hepática Aguda/diagnóstico , Doença Aguda , Injúria Renal Aguda/diagnóstico , Injúria Renal Aguda/etiologia , Injúria Renal Aguda/patologia , Injúria Renal Aguda/terapia , Adolescente , Anemia Hemolítica/etiologia , Anemia Hemolítica/patologia , Anemia Hemolítica/terapia , Terapia Combinada , Feminino , Degeneração Hepatolenticular/complicações , Degeneração Hepatolenticular/patologia , Degeneração Hepatolenticular/terapia , Humanos , Fígado/patologia , Falência Hepática Aguda/etiologia , Falência Hepática Aguda/patologia , Falência Hepática Aguda/terapia , Transplante de Fígado
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