Results 1 to 10 of about 1,526 (151)

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

open access: goldSurgical 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   +4 more sources

Extraocular sebaceous carcinoma in muir-torre syndrome

open access: diamondIndian Journal of Dermatology, 2022
Abbas Albayati   +4 more
doaj   +5 more sources

Myxofibrosarcoma harboring an MLH1 pathogenic germline variant associated with Muir-Torre syndrome: a case report [PDF]

open access: goldHereditary Cancer in Clinical Practice, 2021
Background Muir–Torre syndrome (MTS), which accounts for a small subset (1–3 %) of Lynch syndrome (LS), is an autosomal dominant genetic disorder characterized by sebaceous gland or keratoacanthoma associated with visceral malignancies.
Makoto Nakagawa   +13 more
doaj   +4 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

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

open access: goldCase 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

Muir-Torre syndrome. [PDF]

open access: yesCMAJ, 2016
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).
Mintsoulis D, Beecker J.
europepmc   +6 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

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

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

open access: yesCureus, 2022
A 56-year-old male with a past medical history of arachnoid cysts and with two previous brain operations and a ventriculoperitoneal shunt presented with a large left lower quadrant (LLQ) abdominal mass for one year, growing rapidly for the past three months.
Bui A, Shah S, Winston N, Mahmoud A.
europepmc   +3 more sources

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