1.
Bol. Acad. Nac. Med. B.Aires
;
94(1-2): 154-175, ene.-dic. 2016. ilus, tab, graf
Artículo
en Español
| LILACS
| ID: biblio-997047
Asunto(s)
Humanos , Femenino , Adulto , Persona de Mediana Edad , Paraproteinemias/diagnóstico , Paraproteinemias/terapia , Cadenas Ligeras de Inmunoglobulina/metabolismo , Cadenas Ligeras de Inmunoglobulina/fisiología , Síndrome de Fanconi/diagnóstico , Síndrome de Fanconi/terapia , Riñón/metabolismo
2.
Indian J Pathol Microbiol
;
2006 Oct; 49(4): 557-9
Artículo
en Inglés
| IMSEAR
| ID: sea-73257
RESUMEN
Hepatic involvement in primary amyloidosis is not rare but is often clinically silent. A mild elevation of the serum alkaline phosphatase level and hepatomegaly are the most common findings. We report a case of primary amyloidosis in an adult male presenting with intrahepatic cholestasis where viral, drug, alcohol, and autoimmune etiologies were all excluded and the definite diagnosis was established by liver biopsy with Congo red staining. Subsequently the patient was found to have monoclonal light chain disorder.