Results 41 to 50 of about 3,333 (172)

Ileocecal Adenocarcinoma and Ureteral Transitional Cell Carcinoma with Multiple Sebaceous Tumors and Keratoacanthomas in a Case of Muir-Torre Syndrome [PDF]

open access: yesDermatology Research and Practice, 2010
Cutaneous neoplasms including sebaceous tumors, keratoacanthomas, and basal cell carcinomas with sebaceous differentiation can be markers of internal malignancy associated with the Muir-Torre Syndrome (MTS).
Michael C. Lynch, Bryan E. Anderson
doaj   +2 more sources

Muir-Torre syndrome: A case report and review of the literature

open access: yesThe Turkish Journal of Gastroenterology, 2012
Muir-Torre syndrome is a rare autosomal dominant genodermatosis characterized by the occurrence of sebaceous gland neoplasm associated with visceral malignancies.
Gökhan OKAN   +5 more
doaj   +2 more sources

Sebaceous Neoplasms

open access: yesDiagnostics, 2023
Sebaceous neoplasms describe a group of tumors with sebaceous differentiation commonly seen in lesions located primarily in the face and neck. The majority of these lesions are benign, while malignant neoplasms with sebaceous differentiation are uncommon.
Ilias Papadimitriou   +5 more
doaj   +1 more source

Case for diagnosis. Verrucous plaque on the pubic region, [PDF]

open access: yesAnais Brasileiros de Dermatologia, 2021
Muir-Torre syndrome is a rare, autosomal dominant genodermatosis, characterized by sebaceous neoplasms and visceral carcinomas. The authors describe the case of a patient who, 16 years after the diagnosis of colon carcinoma, presented a verrucous plaque ...
Diego Henrique Morais Silva   +3 more
doaj   +1 more source

Multiple sebaceous tumors in a 58‐year‐old man with colorectal cancer

open access: yesClinical Case Reports, 2022
The Muir‐Torre Syndrome is a rare genodermatosis, defined by the occurrence of sebaceous neoplasia and internal malignancies and caused by mutations in the mismatch repair gene.
Mohamed Ben Rejeb   +6 more
doaj   +1 more source

Muir-Torre Syndrome

open access: yesArchives of Pathology & Laboratory Medicine, 2014
Muir-Torre syndrome (MTS) is a rare autosomal-dominant genodermatosis characterized by sebaceous neoplasms and one or more visceral malignancies. Sebaceous tumors include sebaceous adenoma and carcinoma, which may be solitary or multiple. Visceral malignancies most often arise in the colorectum and endometrium.
Feriyl, Bhaijee, Alexandra S, Brown
openaire   +3 more sources

Muir-Torre syndrome - Treatment with isotretinoin and interferon alpha-2a can prevent tumour development [PDF]

open access: yes, 2000
Muir-Torre syndrome is a genodermatosis in which multiple internal malignancies are associated with cutaneous sebaceous tumours and kerato-acanthomas. A 57-year-old man presented with multiple sebaceous tumours, kerato-acanthomas, verrucous carcinoma of ...
Graefe, Tim   +3 more
core   +1 more source

Muir-Torre syndrome

open access: yesDermatology Online Journal, 2006
A 65-year-old man with a history of multiple neoplastic and pre-neoplastic gastrointestinal lesions as well as urogenital carcinoma presented for evaluation of two asymptomatic skin-colored papules in the head and neck region. Biopsy revealed sebaceous neoplasms and immunohistochemical staining was negative for the presence of hMSH-2 protein in both ...
Navi, Daniel   +3 more
openaire   +4 more sources

Muir-Torre Syndrome [PDF]

open access: yes, 2020
A 64-year-old man was referred to our dermatology clinic with a diagnosis of Muir-Torre syndrome (MTS), he had a history of multiple sebaceous carcinomas and sebaceous adenomas removed over the years.
Uzoma, Miranda   +7 more
core   +5 more sources

A rare extraocular sebaceous carcinoma mimicking primary ectopic breast cancer

open access: yesHuman Pathology: Case Reports, 2020
Sebaceous carcinoma (SC) is an aggressive malignancy derived from the sebaceous glands. SC is divided into two categories, ocular and extraocular. Extraocular SC is quite rare, and is also associated with the Muir-Torre syndrome, which is regarded as a ...
Yuri Noda   +6 more
doaj   +1 more source

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