Results 21 to 30 of about 3,333 (172)

A Case of Muir-Torre Syndrome [PDF]

open access: yesCureus, 2021
Muir-Torre syndrome (MTS) is an autosomal dominant condition characterized by dermatological tumors along with visceral malignancies. The dermatological manifestations include recurrent sebaceous adenomas and keratoacanthomas. The commonly seen visceral malignancies are colorectal, gynecological, and urological.
Sheth, Radhika   +2 more
openaire   +3 more sources

Case Report: A Frameshift Mutation in MSH2 Exon 2 in a Kidney Recipient With Muir–Torre Syndrome [PDF]

open access: yesFrontiers in Oncology, 2021
Muir–Torre syndrome (MTS), a rare subtype of Lynch syndrome, is mostly autosomal dominant, which is caused by germline mutations in DNA mismatch repair (MMR) genes, the resulting microsatellite instability (MSI) of which increases the risk of developing ...
Yifei Feng, Jianqing Feng, Jianrong Bao
doaj   +2 more sources

FDG-PET-positive lower-extremity sebaceous-gland carcinoma in a patient with Muir-Torre syndrome

open access: yesRadiology 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   +4 more sources

Muir–Torre syndrome [PDF]

open access: yesCanadian Medical Association Journal, 2015
A 64-year-old woman with a history of colon and cervical cancer presented with a six-month history of episodes of small, raised papules on her face. Her family history included cervical cancer (her sister) and gastric cancer (her father).
Danielle, Mintsoulis, Jennifer, Beecker
openaire   +3 more sources

Muir–Torre syndrome: sebaceous carcinoma concurrent with colon cancer in a kidney transplant recipient; a case report [PDF]

open access: yesBMC Nephrology, 2019
Background Sebaceous carcinoma is a rare but progressive malignant skin cancer, and the incidence is approximately five times higher in post-transplant patients than in people who have not received kidney transplants.
Masahiro Tomonari   +15 more
doaj   +2 more sources

Papillary Renal Cell Carcinoma in Lynch/Muir-Torre Syndrome with Germline Pathogenic Variant in MSH6 and Molecular Analysis [PDF]

open access: yesJournal of Kidney Cancer and VHL, 2021
Lynch syndrome (LS) is an autosomal dominant inherited disorder due to pathogenic variations in the mismatch repair genes, which predisposes to malignancies, most commonly colon and endometrial carcinoma.
Yu Yang   +3 more
doaj   +2 more sources

A case report of Muir–Torre syndrome (MTS) in a Chinese patient [PDF]

open access: yesBMC Ophthalmology
Background Muir-Torre syndrome is a rare disorder characterized by patients suffering from sebaceous gland tumors or keratoacanthoma and visceral malignancies. More cases have been reported in Europe than in Asia.
Jing Wang   +3 more
doaj   +2 more sources

Muir-Torre syndrome in Fitzpatrick skin phototype V assessed by dermoscopy and reflectance confocal microscopy. [PDF]

open access: yesSkin Res Technol
Skin Research and Technology, Volume 30, Issue 8, August 2024.
Orloff J   +7 more
europepmc   +2 more sources

Multiple Eruptive Sebaceous Hyperplasia Secondary to Muir-Torre Syndrome Treated With Fractional Carbon Dioxide Laser Resurfacing Technique: A Case Report. [PDF]

open access: yesSkin Res Technol
Skin Research and Technology, Volume 30, Issue 10, October 2024.
Leuzzi M   +8 more
europepmc   +2 more sources

Urothelial Carcinoma Recurrence in an Ileal Neobladder Nine Years after Primary Surgery with Muir-Torre Syndrome [PDF]

open access: yesCase 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

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