Volume 58, Issue 5 pp. 806-809
Brief Report

Successful pulmonary artery embolectomy in a patient with a saddle Wilms tumor embolus

Lindsey Cooper MD

Corresponding Author

Lindsey Cooper MD

Section of Critical Care, The Children's Hospital and University of Colorado Denver School of Medicine, Aurora, Colorado

Critical Care, Mail Stop 8414, 13121 E. 17th Avenue, P.O. Box 6508, Aurora, Colorado 80045.===Search for more papers by this author
Colin Moore MD

Colin Moore MD

Center for Cancer and Blood Disorders, The Children's Hospital and University of Colorado Denver School of Medicine, Aurora, Colorado

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Brian Branchford MD

Brian Branchford MD

Center for Cancer and Blood Disorders, The Children's Hospital and University of Colorado Denver School of Medicine, Aurora, Colorado

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Brian Greffe MD

Brian Greffe MD

Center for Cancer and Blood Disorders, The Children's Hospital and University of Colorado Denver School of Medicine, Aurora, Colorado

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Kelley Capocelli MD

Kelley Capocelli MD

Section of Pathology, The Children's Hospital and University of Colorado Denver School of Medicine, Aurora, Colorado

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Austine Kuder MD

Austine Kuder MD

Section of General Pediatrics, The Children's Hospital and University of Colorado Denver School of Medicine, Aurora, Colorado

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Inder Mehta MD

Inder Mehta MD

Section of Pediatric Cardiovascular Surgery, The Children's Hospital and University of Colorado Denver School of Medicine, Aurora, Colorado

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Peter M Mourani MD

Peter M Mourani MD

Section of Critical Care, The Children's Hospital and University of Colorado Denver School of Medicine, Aurora, Colorado

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First published: 16 June 2011
Citations: 4

Conflict of interest: Nothing to declare.

Abstract

Denys–Drash syndrome is a genetic disorder characterized by ambiguous genitalia, cryptorchidism, nephrotic syndrome, and a high predilection for Wilms tumor with intravascular invasion. We report a 5-year-old male with Denys–Drash syndrome who rapidly developed Wilms tumor with vascular invasion, subsequent saddle tumor embolus, and required emergent embolectomy. This case illustrates the rapid emergence of Wilms tumor in a patient with Denys–Drash syndrome and the importance of considering embolectomy over thrombolytic therapy for PE in this population, given a high likelihood of tumor embolus. Pediatr Blood Cancer 2012; 58: 806–809. © 2011 Wiley Periodicals, Inc.

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