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Budd-Chiari syndrome secondary to hepatic vein thrombus from Wilm's tumor. Case report and literature review

Jose, B.; Narayan, P.I.; Pietsch, J.B.; Nagaraj, H.S.; Patel, C.C.; Bertolone, S.J.; Spanos, W.J.; Lindberg, R.; Paris, K.J.

Journal of the Kentucky Medical Association 87(4): 174-176

1989

ISSN/ISBN: 0023-0294
PMID: 2542421
Document Number: 341594
We describe a case of Budd-Chiari Syndrome in a 6-year-old boy secondary to Wilm's tumor. The patient had a right nephrectomy and mediastinotomy with removal of the tumor from the right atrium, inferior vena cava, and hepatic vein. Postoperatively, the patient had chemotherapy consisting of Actinomycin-D to be followed by radiation to the tumor bed to a total dose of 2000 rads in 10 fractions by using AP/PA field on 6 MeV Linear Accelerator. Currently, the child is receiving combination chemotherapy.

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