Well-concealed advanced duodenal carcinoma with Muir–Torre syndrome: a case report and review of literature [PDF]
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
Abbas Albayati +4 more
doaj +5 more sources
Myxofibrosarcoma harboring an MLH1 pathogenic germline variant associated with Muir-Torre syndrome: a case report [PDF]
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]
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]
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
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]
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]
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]
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]
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

