Immunohistochemical Screening of Upper Tract Urothelial Carcinomas for Lynch Syndrome Diagnostics: A Systematic Review
Author:
Funder
Danish Cancer Society Research Center
Danish Cancer Society
Publisher
Elsevier BV
Subject
Urology
Reference41 articles.
1. Cancer risks by gene, age, and gender in 6350 carriers of pathogenic mismatch repair variants: findings from the Prospective Lynch Syndrome Database;Dominguez-Valentin;Genet Med,2020
2. Risk of urothelial bladder cancer in Lynch syndrome is increased, in particular among MSH2 mutation carriers;van der Post;J Med Genet,2010
3. Urinary tract cancer in lynch syndrome; increased risk in carriers of MSH2 mutations;Joost;Urology,2015
4. A proportion of hereditary upper urinary tract urothelial carcinomas are misclassified as sporadic according to a multi-institutional database analysis: proposal of patient-specific risk identification tool;Audenet;BJU Int,2012
5. Hollenbeak CS. Incidence and survival of patients with carcinoma of the ureter and renal pelvis in the USA, 1973-2005;Raman;BJU Int,2011
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1. Pathology focused review of morphologic subtypes and molecular variants of urothelial carcinoma with an emphasis on clinical/treatment relevance;Urologic Oncology: Seminars and Original Investigations;2024-07
2. A collaborative review of the microsatellite instability/deficient mismatch repair phenotype in patients with upper tract urothelial carcinoma;BJU International;2024-05-30
3. Mismatch repair deficiency and microsatellite instability in urothelial carcinoma: a systematic review and meta-analysis;BMJ Oncology;2024-04
4. Contemporary Issues in Urothelial Carcinoma of Upper Urinary Tract;Advances in Anatomic Pathology;2023-11-27
5. Lynch syndrome-associated upper tract urothelial carcinoma frequently occurs in patients older than 60 years: an opportunity to revisit urology clinical guidelines;Virchows Archiv;2023-08-23
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