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Updated: Jun 26, 2026

A Patient-Derived Xenograft Model for Venous Malformation
Published on: June 15, 2020
Acquired factor VII deficiency associated with Wilms tumor
Jeremy Granger1, Vinod K Gidvani
1Department of Pediatrics, Wilford Hall Medical Center, Lackland AFB, Texas 78236, USA. jeremy.granger@lackland.af.mil
Abstract:
We present the case of a 2-year-old female with Wilms tumor whose initial evaluation revealed a prolonged prothrombin time (PT) and normal activated partial thromboplastin time. Mixing studies demonstrated correction of the PT and the Factor VII activity was 17% in the absence of a Factor VII inhibitor. She underwent successful resection of the tumor with fresh frozen plasma support and no excessive bleeding. Post-operative testing demonstrated normal PT at 3 days and 1-month. Although acquired von Willebrand factor deficiency has a known association with Wilms tumor, paraneoplastic factor VII deficiency associated with Wilms tumor is previously unreported.
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