[AL amyloidosis associated with multiple myeloma revealed by cholestatic hepatomegaly: A case report].
INTRODUCTION AL amyloidosis is a rare disorder characterized by the extracellular deposition of immunoglobulin light chain fibrils produced by a clonal plasma cell population. Hepatic involvement as the initial manifestation is rare, and forms associated with jaundice and cholestasis carry a poor prognosis. CASE REPO...