DNA mismatch repair‐deficient non‐neoplastic endometrial glands are common in Lynch syndrome patients and are present at a higher density than in the colon
Author:
Affiliation:
1. Department of Pathology University of Pittsburgh Medical Center Pittsburgh PAUSA
2. Department of Medicine University of Pittsburgh Medical Center Pittsburgh PA USA
Publisher
Wiley
Subject
General Medicine,Histology,Pathology and Forensic Medicine
Link
https://onlinelibrary.wiley.com/doi/pdf/10.1111/his.14386
Reference26 articles.
1. American Gastroenterological Association Technical Review on the Diagnosis and Management of Lynch Syndrome
2. Screening for the Lynch Syndrome (Hereditary Nonpolyposis Colorectal Cancer)
3. Phenotypic and genotypic heterogeneity in the Lynch syndrome: diagnostic, surveillance and management implications
4. Recommendations from the EGAPP Working Group: genetic testing strategies in newly diagnosed individuals with colorectal cancer aimed at reducing morbidity and mortality from Lynch syndrome in relatives
5. Screening for Lynch Syndrome (Hereditary Nonpolyposis Colorectal Cancer) among Endometrial Cancer Patients
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1. Highly Sensitive Microsatellite Instability and Immunohistochemistry Assessment in Endometrial Aspirates as a Tool for Cancer Risk Individualization in Lynch Syndrome;Modern Pathology;2023-07
2. Mismatch repair protein status of non-neoplastic uterine and intestinal mucosa in patients with Lynch syndrome and double somatic mismatch repair protein mutations;Human Pathology;2023-07
3. Mutation-specific Mismatch Repair–deficient Benign Endometrial Glands in Endometrial Biopsies and Curettings Are a Biomarker of Lynch Syndrome and Associate With Endometrial Carcinoma Development;American Journal of Surgical Pathology;2023-05-25
4. Lynch Syndrome and Gynecologic Tumors: Incidence, Prophylaxis, and Management of Patients with Cancer;Cancers;2023-02-22
5. Lynch Syndrome: From Carcinogenesis to Prevention Interventions;Cancers;2022-08-24
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