Maintenance Intravenous Immunoglobulin Treatment for Multiple Sclerosis Coexisting with Ehlers-Danlos Syndrome and Muir-Torre Syndrome: A Case Study [PDF]
Neurology and Therapy, 2020 The therapeutic options for disease modification in relapsing-remitting multiple sclerosis (RRMS) have expanded remarkably in the last 15 years. Although intravenous immunoglobulins (IVIg) have shown some therapeutic effects in multiple sclerosis ...
Srishti Gupta +2 more
doaj +3 more sources
FDG-PET-positive lower-extremity sebaceous-gland carcinoma in a patient with Muir-Torre syndrome [PDF]
Radiology Case Reports, 2015 Sebaceous-gland carcinoma can occur alone or as one of the defining features of the Muir-Torre syndrome. Cases occurring below the head and neck are extremely rare.
Bina Kviatkovsky, MSc +7 more
doaj +3 more sources
Urothelial Carcinoma Recurrence in an Ileal Neobladder Nine Years after Primary Surgery with Muir-Torre Syndrome [PDF]
Case Reports in Urology, 2016 We report a patient who presented with a urothelial carcinoma recurrence developed nine years after radical cystoprostatectomy, related to Muir-Torre syndrome.
Floryn Cherbanyk +5 more
doaj +2 more sources
Hereditary Cancer in Clinical Practice, 2017 Background The tumor spectrum in the Lynch syndrome is well defined, comprising an increased risk of developing colonic and extracolonic malignancies. Muir-Torre syndrome is a variant with a higher risk of skin disease.
Caroline Kientz +9 more
doaj +2 more sources
Clinical and Molecular Features of Skin Malignancies in Muir-Torre Syndrome. [PDF]
Genes (Basel), 2021 Background: We investigated the mutational landscape of skin tumors in patients with Muir-Torre Syndrome (MTS) a hereditary autosomal dominant mismatch repair disorder of increased cancer susceptibility, and examined mutations other than in the DNA ...
Simic D +4 more
europepmc +6 more sources
Muir-Torre Syndrome: case report and molecular characterization
São Paulo Medical JournalCONTEXT: Muir-Torre syndrome is a rare autosomal dominant genodermatosis caused by mutations in the mismatch repair genes. It is characterized by the presence of sebaceous skin tumors and internal malignancies, affecting mainly the colon, rectum and ...
Carolina Alejandra Rios +4 more
doaj +2 more sources
Sebaceomas in a Muir–Torre-like Phenotype in a Patient with MUTYH-Associated Polyposis
DermatopathologyThis 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 +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 +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 +2 more
doaj +2 more sources
Extraocular sebaceous carcinoma in muir-torre syndrome
Indian Journal of Dermatology, 2022 Abbas Albayati +4 more
doaj +2 more sources