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Budd-Chiari syndrome secondary to inflammatory pseudotumor of the liver: Report of a case with a 10-year follow-up

Ramírez-de-la-Piscina, P.; Estrada, S.; Calderón, R.; Duca, I.; Spicakova, K.; Delgado, E.; Zabaleta, S.; Bengoa, R.; García-Campos, F.

Revista Espanola de Enfermedades Digestivas Organo Oficial de la Sociedad Espanola de Patologia Digestiva 105(6): 360-362

2013

ISSN/ISBN: 1130-0108
PMID: 24090020
Document Number: 664007
Inflammatory pseudotumor (IPT) of the liver is a rare benign tumor of unknown origin, it has the appearance of a malignant tumor but has a benign histology and clinical course. We report a case of a 63-year-old man diagnosed of IPT of the liver and followed for 10 years. During the clinical course, he developed a secondary Budd-Chiari syndrome, with a successful response to a transjugular intrahepatic portosystemic shunt over a 5-year follow-up period.

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