门脉高压
医学
肝病学
腹水
疾病
单克隆抗体病
肝病
病理
罕见病
内科学
胃肠病学
单克隆
肝硬化
免疫学
单克隆抗体
抗体
作者
Molly Delk,Fredric Regenstein
出处
期刊:Hepatology
[Lippincott Williams & Wilkins]
日期:2021-08-27
卷期号:74 (6): 3546-3548
被引量:4
摘要
Light chain deposition disease (LCDD) is a rare entity that is generally discovered in the setting of solid organ dysfunction. The monoclonal gammopathy leads to abnormal deposition of light chains in tissues, most often manifested by way of renal dysfunction. Other organ systems may also be affected, the liver being the second‐most common after the kidneys. Liver involvement rarely leads to clinically significant disease, with few case reports in the literature. We present the case of a patient referred to a hepatology clinic for the evaluation of new‐onset ascites resulting from portal hypertension secondary to LCDD involving the liver.
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