GU Syndromic Associations: Case-Based Review and Next Steps After Diagnosis

This lecture will review genitourinary (GU) syndromic associations using real cases as examples. The topics included are von Hippel Lindau, hereditary papillary renal cell carcinoma, fumarate hydratase deficiency/hereditary leiomyomatosis and renal cell carcinoma, and succinate dehydrogenase deficiency. The lecture reviews some of the GU-associated tumors for each syndrome with a particular focus on the guidelines for referral to genetic counseling and further genetic testing. Also included are discussions of challenging immunohistochemistry interpretations and other ancillary tests that may help make these diagnoses or suggest referral for molecular genetic confirmation. At least two nonclassical presentations are also discussed with discussion about the implication of these findings and suggestions for increased rate of detection.

Lecture Presenter
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Jonathon Mahlow, MD
Jonathon Mahlow, MD
Assistant Professor, University of Utah School of Medicine
Medical Director, Anatomic Pathology, ARUP Laboratories

Dr. Mahlow is a staff pathologist at ARUP and an assistant professor of pathology at the University of Utah School of Medicine. He received his MD from Wayne State School of Medicine in Detroit and completed his anatomic and clinical pathology residency training at the Cleveland Clinic Foundation in Cleveland. Subsequently, he completed a fellowship in surgical pathology at the University of Utah. Dr. Mahlow is a member of several professional societies, including the United States and Canadian Academy of Pathology, and the American Society for Clinical Pathology.

Objectives

After this presentation, participants will be able to:

Review GU cancer syndromes
Explain morphologic, immunohistochemical, FISH, and other ancillary methods related to syndromic diagnosis/detection
Review NCCN 2023 genetic testing guidelines, with particular attention to pathologic diagnosis
Review unusual presentations of rare syndromes