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Intern Med ; 63(1): 71-75, 2024 Jan 01.
Artigo em Inglês | MEDLINE | ID: mdl-37121747

RESUMO

A 73-year-old woman was referred to our hospital for persistent liver dysfunction. When the patient was 45 years old, her youngest sister had been diagnosed with Wilson disease (WD). The patient therefore underwent several family screening tests, all of which were unremarkable. She had an annual medical checkup and was diagnosed with liver dysfunction and fatty liver at 68 years old. A liver biopsy and genetic testing were performed, and she was diagnosed with WD; chelation therapy was then initiated. In patients with hepatic disorders and a family history of WD, multiple medical examinations should be conducted, as the development of WD is possible regardless of age.


Assuntos
Degeneração Hepatolenticular , Hepatopatia Gordurosa não Alcoólica , Feminino , Humanos , Idoso , Pessoa de Meia-Idade , Degeneração Hepatolenticular/complicações , Degeneração Hepatolenticular/diagnóstico , Degeneração Hepatolenticular/tratamento farmacológico , Hepatopatia Gordurosa não Alcoólica/complicações , Hepatopatia Gordurosa não Alcoólica/diagnóstico , Testes Genéticos , Cobre , Pacientes
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