Results 21 to 30 of about 1,372,625 (169)

Glioblastoma multiforme in the Muir–Torre syndrome [PDF]

Clinical Neurology and Neurosurgery, 2011
Muir-Torre syndrome (MTS) is an autosomal dominant subtype of nonpolyposis colorectal carcinoma (HNPCC) characterized by the development of sebaceous gland tumors and visceral malignancies. The most common subtype of MTS is characterized by germline mutations in mismatch repair (MMR) genes leading to microsatellite instability (MSI).
Zev A, Binder, Michael W, Johnson, Avadhut, Joshi, Christine L, Hann, Constance A, Griffin, Alessandro, Olivi, Gregory J, Riggins, Gary L, Gallia   +7 more
core   +4 more sources

Sebaceomas in a Muir–Torre-like Phenotype in a Patient with MUTYH-Associated Polyposis

Dermatopathology
This case report describes a case of a patient with MUTYH-associated polyposis (MAP), who presented with multiple sebaceomas in a Muir–Torre-like phenotype.
Julia Guarrera, James C. Prezzano, Kathleen A. Mannava   +2 more
doaj   +2 more sources

Postradiation Histiocytic Sarcoma in the Setting of Muir-Torre Syndrome [PDF]

Case Reports in Pathology, 2018
Hereditary nonpolyposis colorectal carcinoma (HNPCC) is an autosomal dominant genetic disorder characterized by a predisposition towards colorectal carcinoma and other extracolonic neoplasms.
Erin Baumgartner, David Ullman, Jeffrey Adam Jones, Danielle Fasciano, Daniel S. Atherton, Peter Pavlidakey, Deniz Peker   +6 more
doaj   +2 more sources

Generational Expression of Muir-Torre Syndrome in a Canadian Family [PDF]

Case Reports in Dermatological Medicine, 2016
Muir-Torre syndrome (MTS) is a rare autosomal dominant inherited genodermatosis that is considered to be a phenotypic subtype of hereditary nonpolyposis colorectal cancer (HNPCC), commonly referred to as Lynch syndrome. We describe the clinical course of
Kaitlin Alexandra Vanderbeck, R. Gary Sibbald, Nirosha Murugan   +2 more
doaj   +2 more sources

Extraocular sebaceous carcinoma in muir-torre syndrome

Indian Journal of Dermatology, 2022
Abbas Albayati, Burak Ozkan, Ebru Sebnem Ayva, Ahmet Cagri Uysal, Nilgun Markal Ertas   +4 more
doaj   +2 more sources

Muir-Torre Syndrome Associated With a Cryptic Intronic MSH2 Variant Identified via Whole-Genome Sequencing: A Case Report. [PDF]

Pathol Int
Pathological suspicion persisted despite negative multigene panel testing in a patient with synchronous sebaceous and colonic tumors showing concordant MSH2/MSH6 loss. Whole‐genome sequencing identified a cryptic intronic MSH2 variant (c.2459‐12A>G), and RNA analysis confirmed aberrant splicing with protein truncation. This case highlights the value of
Noda K, Kurohama H, Matsuda K, Kinoshita A, Mishima H, Matsumoto M, Matsuda R, Ueki N, Kishikawa M, Miura K, Nonaka T, Yoshiura KI, Matsumoto K, Nakashima M.   +13 more
europepmc   +2 more sources

Muir-Torre syndrome in a haemodialysis patient. [PDF]

Clin Kidney J, 2013
Muir-Torre syndrome (MTS) is a rare inherited cancer syndrome with variable penetrance. MTS follows an autosomal-dominant pattern of inheritance, and is a subtype of Lynch syndrome [formally known as hereditary non-polyposis colorectal cancer (HNPCC)]. MTS is caused by mutations in one of several mismatch repair genes.
Godfrey ED, Coward RA, Gharpuray-Pandit D, Lalloo F, McKirdy S, Woywodt A.   +5 more
europepmc   +4 more sources

Muir-Torre syndrome [PDF]

, 2020
A 64-year-old man was referred to our dermatology clinic with a diagnosis of Muir-Torre syndrome (MTS), he had a history of multiple sebaceous carcinomas and sebaceous adenomas removed over the years.
Uzoma, Miranda, Gamret, A Caresse, Romanelli, Paolo, Gaudi, Sudeep, Jahan-Tigh, Richard R, Klingbeil, Kyle D, Fertig, Raymond M, Silapunt, Sirunya   +7 more
core   +9 more sources

Muir Torre syndrome and in vitro fertilization: One family's experience [PDF]

JAAD Case Reports, 2020
Surget Cox, MD, Janellen Smith, MD
doaj   +2 more sources

Muir-Torre syndrome: A case report and review of the literature

The Turkish Journal of Gastroenterology, 2012
Muir-Torre syndrome is a rare autosomal dominant genodermatosis characterized by the occurrence of sebaceous gland neoplasm associated with visceral malignancies.
Gökhan OKAN, Pervin VURAL, Ümit İNCE, Aziz YAZAR, Cihan URAS, Murat SARUÇ   +5 more
doaj   +2 more sources