{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,5,12]],"date-time":"2026-05-12T18:09:56Z","timestamp":1778609396816,"version":"3.51.4"},"reference-count":6,"publisher":"Ovid Technologies (Wolters Kluwer Health)","issue":"6","license":[{"start":{"date-parts":[[2021,10,23]],"date-time":"2021-10-23T00:00:00Z","timestamp":1634947200000},"content-version":"vor","delay-in-days":0,"URL":"http:\/\/onlinelibrary.wiley.com\/termsAndConditions#vor"},{"start":{"date-parts":[[2021,10,23]],"date-time":"2021-10-23T00:00:00Z","timestamp":1634947200000},"content-version":"tdm","delay-in-days":0,"URL":"http:\/\/doi.wiley.com\/10.1002\/tdm_license_1.1"}],"content-domain":{"domain":["lww.com","ovid.com"],"crossmark-restriction":true},"short-container-title":["Hepatology"],"published-print":{"date-parts":[[2021,12]]},"abstract":"<jats:p>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\u2010most 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\u2010onset ascites resulting from portal hypertension secondary to LCDD involving the liver.<\/jats:p>","DOI":"10.1002\/hep.32118","type":"journal-article","created":{"date-parts":[[2021,8,27]],"date-time":"2021-08-27T04:25:36Z","timestamp":1630038336000},"page":"3546-3548","update-policy":"https:\/\/doi.org\/10.1097\/lww.0000000000001000","source":"Crossref","is-referenced-by-count":5,"title":["Light Chain Deposition Disease: An Unusual Cause of Portal Hypertension"],"prefix":"10.1097","volume":"74","author":[{"ORCID":"https:\/\/orcid.org\/0000-0002-5825-9192","authenticated-orcid":false,"given":"Molly Delk","family":"Plummer","sequence":"first","affiliation":[{"name":"Division of Abdominal Transplant,Tulane University School of Medicine,New Orleans,LA"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Fredric","family":"Regenstein","sequence":"additional","affiliation":[{"name":"Division of Abdominal Transplant,Tulane University School of Medicine,New Orleans,LA"}],"role":[{"role":"author","vocabulary":"crossref"}]}],"member":"276","published-online":{"date-parts":[[2021,10,23]]},"reference":[{"key":"hep32118-bib-0001-20250824","doi-asserted-by":"crossref","first-page":"293","DOI":"10.1016\/0002-9343(76)90440-X","article-title":"Manifestations of systemic light chain deposition","volume":"60","year":"1976","journal-title":"Am J Med"},{"key":"hep32118-bib-0002-20250824","doi-asserted-by":"crossref","first-page":"1235","DOI":"10.1016\/S0889-8588(05)70123-4","article-title":"Nonamyloidotic monoclonal immunoglobulin deposition disease. 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