ArticleCureus2025
Budd-Chiari Syndrome as an Initial Presentation of Essential Thrombocythemia.
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.
What it found
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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.
The trial behind it
Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.
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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
Budd-Chiari syndrome (BCS) is a clinical condition defined by the obstruction of hepatic venous outflow, resulting in portal hypertension and subsequent hepatic dysfunction. The syndrome is frequently associated with prothrombotic states, among which myeloproliferative neoplasms represent the most prevalent underlying etiology. The clinical presentation of BCS is highly variable, ranging from a mild and insidious disease course to an acute condition associated with liver failure. This heterogeneity in presentation often leads to delays in diagnosis. This report describes a rare case of BCS as the first manifestation of essential thrombocythemia (ET) in a young male patient, emphasizing the importance of early diagnosis and multidisciplinary management for better outcomes.
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Registered trials
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