Results 91 to 100 of about 3,333 (172)

Lynch Syndrome and Muir-Torre Syndrome: An update and review on the genetics, epidemiology, and management of two related disorders [PDF]

, 2017
Hereditary Nonpolyposis Colorectal Cancer (HNPCC), also known as Lynch Syndrome, is an autosomal dominant, tumor predisposing disorder usuallycaused by germline mutations in mismatch repair (MMR) genes.
Le, Stephanie, Patel, Parth, Malik, Kunal, Mumtaz, Aisha, Ansari, Umer, Doyle, Amanda, Khachemoune, Amor   +6 more
core   +1 more source

ePosters Virtual

European Journal of Neurology, Volume 33, Issue S1, June 2026.
wiley   +1 more source

Muir–Torre syndrome: case report

Revista da Sociedade Portuguesa de Dermatologia e Venereologia
Muir–Torre syndrome (MTS) is characterized by the association of at least one, but often multiple, sebaceous skin neoplasms, and at least one visceral neoplasm, usually colorectal.
Joana Heitor, Ana R. Afonso, Catarina Antunes, Catarina Correia, André Lencastre   +4 more
doaj  

Historical review of Lynch syndrome

Journal of Coloproctology, 2013
Lynch syndrome was formerly known as Hereditary Nonpolyposis Colorectal Cancer. Currently, these two nomenclatures each have their unique definitions and are no longer used interchangeably.
Andrew I. Wolf, Adam H. Buchanan, Linda M. Farkas   +2 more
doaj   +1 more source

The role of Mohs surgery in the management of benign sebaceous neoplasms

SAGE Open Medical Case Reports
Sebaceoma is a benign sebaceous neoplasm with rare potential for malignant transformation. We report a case of recurrent sebaceoma in a 70-year-old male with Muir–Torre syndrome, successfully treated with Mohs micrographic surgery.
Ghassan Barnawi, Sarah Aly, Noha Benharira, Ammar Saed Aldien, Mohammed Barasheed, Manish Khanna   +5 more
doaj   +1 more source

Multiple schwannomas, including a plexiform variant, in a patient in the absence of neurofibromatosis I or II

Journal of the Scientific Society, 2015
Multiple schwannomatosis, is defined as two or more, pathologically proven schwannomas, without radiographic evidence of vestibular nerve tumor, below 18 years, or absence of VIII nerve dysfunction beyond 30 years with absence of stigmata of ...
Snehlata R Hingway
doaj   +1 more source

Looking beyond the surface: Muir Torre syndrome. [PDF]

Arch Clin Cases, 2023
Bagga E, Innes D, Leung E, Leung E.
europepmc   +1 more source

UEG Week 2025 Poster Presentations

United European Gastroenterology Journal, Volume 13, Issue S8, Page S803-S1476, October 2025.
wiley   +1 more source

‘‘Second Hit’’ in Sebaceous Tumors from Muir–Torre Patients with Germline Mutations in MSH2: Allele Loss is Not the Preferred Mode of Inactivation

, 2001
Muir–Torre syndrome is an autosomal-dominant inherited disorder predisposing to both sebaceous skin tumors and internal neoplasms. In a significant proportion of Muir–Torre syndrome patients skin tumors exhibit microsatellite instability as a hallmark of
Friedl, Waltraut, Bisceglia, Michele, Kruse, Roland, Rütten, Arno, Hosseiny-Malayeri, Hamid R., Ruzicka, Thomas, Propping, Peter, Mangold, Elisabeth   +7 more
core   +1 more source

Muir-Torre Syndrome: Abdominal Sebaceous Carcinoma. [PDF]

Cureus, 2022
Bui A, Shah S, Winston N, Mahmoud A.
europepmc   +1 more source