ArticleCureus2025
Hepatic Amyloidosis Manifesting as Budd-Chiari Syndrome: An Unusual Presentation.
Article in Cureus, 2025. 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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0 citing papers in PubMed.
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Authors and funding
5 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Amyloidosis is a rare infiltrative multisystemic disorder characterized by protein misfolding, leading to progressive organ failure. It can be either acquired or hereditary. Very few case reports regarding hepatic amyloidosis with Budd-Chiari syndrome have been reported up to date. We report the case of a 45-year-old man presenting with abdominal distension, pain in the abdomen, and jaundice. Through right hepatic vein cannulation, HVPG (hepatic venous pressure gradient) was found to be 10 mmHg. The liver biopsy revealed near-total replacement of hepatic parenchyma by amorphous congophilic deposits with obliteration of sinusoids. Hepatic amyloidosis with hepatic venous occlusion is a rare entity.
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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.