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Well-concealed advanced duodenal carcinoma with Muir–Torre syndrome: a case report and review of literature [PDF]

open access: yesSurgical Case Reports, 2023
Background Muir–Torre syndrome is an autosomal-dominant mutation in mismatch repair genes that gives rise to sebaceous tumors and visceral malignancies over time.
Tomoyuki Sugi   +9 more
doaj   +2 more sources

Sebaceous Carcinoma of the Eyelid and Muir-Torre Syndrome [PDF]

open access: yesActa Clinica Croatica, 2023
Muir-Torre syndrome is a rare form of hereditary nonpolyposis colorectal cancer syndrome; simplified, it is an association of at least one sebaceous skin tumor and at least one visceral malignancy.
Karla Ranđelović   +6 more
doaj   +2 more sources

Extraocular cutaneous sebaceous carcinoma in a patient with Muir-Torre syndrome: special emphasis on histologic and dermoscopic features [PDF]

open access: yesDermatology Reports, 2023
Cutaneous sebaceous carcinoma can be classified into periocular and extraocular and can occur as part of Muir Torre syndrome. It is usually a pink-red or yellow solitary nodule, mainly located in the head and neck region.
Francesco Savoia   +6 more
doaj   +2 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

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   +4 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: The Importance of a Detailed Family History [PDF]

open access: yesCase Reports in Ophthalmology, 2019
Muir-Torre syndrome, a variant of Lynch syndrome or hereditary nonpolyposis colorectal cancer, is an autosomal dominant disease characterized by skin neoplasms (sebaceous or keratoacanthomas) and visceral malignancies.
Christopher K.H. Burris   +7 more
doaj   +2 more sources

The role of immunohistochemistry in the Muir-Torre Syndrome [PDF]

open access: yesAnais Brasileiros de Dermatologia, 2015
Muir-Torre Syndrome is defined by the coexistence of sebaceous skin tumors and internal malignancies. Mutations in the DNA mismatch repair genes are found in the inherited form of the disease, resulting in the absence of crucial enzymes involved with DNA
Cláudia Marina Puga Barbosa Oliveira   +4 more
doaj   +2 more sources

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