ArticleACG case reports journal2026
Hepatic Amyloid Light-Chain Amyloidosis Incidentally Diagnosed via Endoscopic Ultrasound-Guided Liver Biopsy.
Article in ACG case reports journal, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.
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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
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8 authors.
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Abstract
Hepatic amyloid light-chain (AL) amyloidosis is characterized by amyloid protein deposition in the liver, requiring biopsy for diagnosis. We report a 71-year-old man with lymphoplasmacytic lymphoma/Waldenström macroglobulinemia presenting with hepatomegaly and elevated enzymes. Imaging revealed no masses. The patient was diagnosed with hepatic AL amyloidosis through repeat endoscopic ultrasound-guided liver biopsy (EUS-LB), following an initial inconclusive result. A postprocedural hepatic hematoma resolved within 2 months. To the best of our knowledge, cases of hepatic AL amyloidosis diagnosed through EUS-LB are scarce. This case illustrates the diagnostic utility of EUS-LB in hepatic AL amyloidosis and highlights the need for careful interpretation of postprocedural findings.
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