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A subtype of inflammatory pseudotumor of the liver characterized by a benign, well-circumscribed tumor with fibrohistiocytic infiltration (including xanthogranulomatous inflammation, multinucleated giant cells, and neutrophilic infiltration), typically localized in the peripheral hepatic parenchyma. Presentation may be of non-specific symptoms (fever, malaise, and abdominal pain) or as an incidental finding.
Estimated prevalence: Unknown (Unknown prevalence).
Data assembled from 2 of 12 sources · Last updated Sep 20, 2026, 11:34 PM UTC
European rare disease database
Genetic and Rare Diseases Info Center