Cristino, Ana and Pais, Carmen and Silva, Renata and Carrola, Paulo (2017) Light-Chain Deposition Disease with Prominent Hepatic Involvement. European Journal of Case Reports in Internal Medicine, 4 (3). ISSN : 2284-2594
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Official URL: http://ejcrim.com/index.php/EJCRIM/article/view/54...
Abstract
Light-chain deposition disease (LCDD) is a rare monoclonal gammopathy that involves the deposition of light chains (LC) in multiple organs, leading to progressive dysfunction. The kidney is usually the most affected organ and responsible for the initial clinical manifestations. We present the case of a patient with LCDD with prominent liver involvement (marked cholestasis, hepatomegaly and portal hypertension) but with no evidence of coexisting lymphoproliferative disorder.
Item Type: | Article |
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Uncontrolled Keywords: | Light-chain deposition; monoclonal; plasma cell |
Subjects: | 600 Tecnologia - Scienze applicate > 610 Medicina e salute (Classificare qui la tecnologia dei servizi medici) > 616 Malattie (classificare qui la Clinica medica, la medicina basata sull'evidenza, la Medicina interna, la Medicina sperimentale) |
Depositing User: | Rebecca D'Amore |
Date Deposited: | 21 Sep 2017 13:01 |
Last Modified: | 21 Sep 2017 13:21 |
URI: | http://eprints.bice.rm.cnr.it/id/eprint/16295 |
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