Very Rare Cancer Consortium Tumor Board Meeting

Please join us for the Very Rare Cancer Consortium Tumor Board Meeting. This new initiative aims to bring cancer researchers across New York to the table to discuss compelling rare cancer cases presented by physicians and scientists from the New York Genome Center’s partner institutions.

WILMS TUMOR
Case Conference and Research Cohort Review

AGENDA
Introduction – Molecular and Clinical Background
Institute Cohort Review
Case Review
Critical Questions

Speakers

• 

  Michael V. Ortiz, MD

  Pediatric Oncologist
  Assistant Professor of Pediatrics
  Memorial Sloan Kettering Cancer Center 

• 

  Brian Robinson, MD

  Chief of Surgical Pathology,
  Co-Chief,  Urologic Pathology
  Weill Cornell Medicine

• 

  Daniel Ramirez, MD

  Chief, Bone and Soft Tissue Pathology, Division of Anatomic Pathology, Department of Pathology and Laboratory Medicine
  Northwell Health

• 

  Helen Remotti, MD

  GI, Pancreatobiliary, and Hepatic Pathology Fellowship Director
  Department of Pathology and Cell Biology
  Columbia University Irving Medical Center

• 

  Darrell J. Yamashiro, MD, PhD

  Chief of the Division of Hematology, Oncology and Stem Cell Transplantation
  Columbia University Irving Medical Center

  "Patient diagnosed at age 5 with recurrence at age 21"

• 

  Carolyn Fein Levy, MD

  Pediatric Hematologist/Oncologist
  Assistant Professor of Pediatrics
  Zucker School of Medicine at Hofstra/Northwell Health

  "Twins with Wilms Tumor"

• 

  Gary Crouch, MD

  Professor of Pediatrics in the Jack Martin Division of Pediatric Hematology-Oncology
  Icahn School of Medicine at Mount Sinai

  "Teenager with stage IV Wilms Tumor"

• 

  Katharine Offer, MD

  Pediatric Hematology-Oncology, Children’s Cancer Institute, Joseph M. Sanzari Children’s Hospital
  Hackensack University Medical Center

  "Beckwith–Wiedemann Syndrome – Bilateral Wilms Tumor"