Self URI: This article is available from https://www.sapd.es/revista/2025/48/4/05/fulltext
Fecha de recepción: 06 Abril 2024
Fecha de aceptación: 24 Abril 2025
Fecha de publicación: 02 Septiembre 2025
A Plaza Fernández
University Hospital Torrecárdenas. Almería.
A Rodríguez Mateua
M Fernández Carrasco
Hepatic amyloidosis is a rare manifestation of a systemic disease characterized by the extracellular deposition of insoluble proteins. It usually presents asymptomatically or with nonspecific symptoms, and cholestatic jaundice is an exceptional finding. We present a clinical case with this form of onset, in which imaging initially suggested a hepatic neoplasm, and the definitive diagnosis was established through liver biopsy.
Keywords: liver amyloidosis, cholestasis.
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