Understanding the Genetic Landscape of Pancreatic Ductal Adenocarcinoma to Support Personalized Medicine: A Systematic Review

A Pantaleo, G Forte, C Fasano, M Lepore Signorile… - Cancers, 2023 - mdpi.com
Simple Summary Pancreatic ductal adenocarcinoma (PDAC) is an aggressive cancer with
high mortality. Most patients present with an advanced stage of the disease, highlighting the …

A survey of the clinicopathological and molecular characteristics of patients with suspected Lynch syndrome in Latin America

BM Rossi, EI Palmero, F López-Kostner, C Sarroca… - Bmc Cancer, 2017 - Springer
Background Genetic counselling and testing for Lynch syndrome (LS) have recently been
introduced in several Latin America countries. We aimed to characterize the clinical …

Considerations on the performance of immunohistochemistry for mismatch repair gene proteins in cases of sebaceous neoplasms and keratoacanthomas with …

A Fernandez-Flores - The American Journal of Dermatopathology, 2012 - journals.lww.com
Cutaneous sebaceous tumors, as well as keratoacanthomas, are associated with Muir–
Torre syndrome (MTS). Visceral neoplasias are a feature of this syndrome; thus, early …

[HTML][HTML] Muir-Torre syndrome

D Navi, A Wadhera, MA Fung… - Dermatology online …, 2006 - escholarship.org
A 65-year-old man with a history of multiple neoplastic and pre-neoplastic gastrointestinal
lesions as well as urogenital carcinoma presented for evaluation of two asymptomatic skin …

[HTML][HTML] Synchronous gastric and sebaceous cancers, a rare manifestation of MLH1-related Muir-Torre syndrome

J Švec, L Schwarzová, B Janošíková… - … Journal of Clinical …, 2014 - ncbi.nlm.nih.gov
Abstract Muir-Torre syndrome (MTS), a rare variant of the hereditary non polyposis
colorectal cancer syndrome, is an autosomal dominant genodermatosis characterised by …

MLH1 and MSH2 mutation screening in HNPCC families of Hungary–Two new MMR gene mutations

M Tanyi, J Olasz, JL Tanyi, L Tóth… - European Journal of …, 2014 - Elsevier
Abstract Introduction Hereditary Non-Polyposis Colorectal Cancer is an inherited disease
with deleterious germline mutations in the DNA mismatch repair genes causing the …

Q48P mutation in the hMLH1 gene associated with Lynch syndrome in three Hungarian families

M Tanyi, J Olasz, JL Tanyi, L Tóth, P Antal-Szalmás… - Familial cancer, 2012 - Springer
Lynch syndrome (Hereditary nonpolyposis colorectal cancer, HNPCC) is an inherited
disease with variable phenotype causing the development of colon cancer and other …

Muir-Torre syndrome caused by exonic deletion of MLH1 due to homologous recombination

M Shiki, T Hida, K Sugano, R Kaneko, T Kamiya… - European Journal of …, 2017 - Springer
Abstract Background Muir-Torre syndrome (MTS) is characterized by sebaceous neoplasms
with internal malignancies and regarded as a variant of hereditary nonpolyposis colorectal …

[HTML][HTML] Muir-Torre syndrome presenting as sebaceous adenocarcinoma and invasive msh6-positive colorectal adenocarcinoma

S Tulpule, H Ibrahim, M Osman, S Zafar… - Case Reports in …, 2016 - karger.com
Muir-Torre syndrome (MTS) is a rare genodermatosis, diagnosed by the presence of
sebaceous neoplasms along with an internal malignancy, most commonly colorectal …

[HTML][HTML] Sebaceous carcinoma of the eyelid in a patient with Muir-Torre syndrome treated with pembrolizumab: A case report

A Abdalla, GR Souza, D Mahadevan - Current Problems in Cancer: Case …, 2022 - Elsevier
Abstract Patients with Muir-Torre Syndrome (MTS) are at increased risk of developing
sebaceous carcinomas besides other visceral malignancies. Pembrolizumab is an effective …