Results 151 to 160 of about 4,369 (198)

Incidence and histological features of colorectal cancer in the Northern Cape province, South Africa [PDF]

open access: yes, 2010
Algar, U.   +5 more
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Muir‐Torre Syndrome

Journal of Dermatology, 1992
AbstractMuir‐Torre syndrome is characterized by multiple sebaceous tumors, various internal malignancies and an autosomal dominant inheritance. We herein report a typical case. The patient was a 69‐year‐old man with sebaceous adenomas, a keratoacanthoma, and actinic keratosis in addition to carcinomas of the prostate, colon, duodenum, and larynx.
H, Narita   +3 more
exaly   +3 more sources

Muir-Torre syndrome

Lancet Oncology, The, 2005
Muir-Torre syndrome is an autosomal-dominant skin condition of genetic origin, characterised by tumours of the sebaceous gland or keratoacanthoma that are associated with visceral malignant diseases. The cutaneous characteristics of Muir-Torre syndrome are sebaceous adenoma, epithelioma, carcinoma, or multiple keratoacanthomas, whereas visceral ...
Giovanni Ponti, Maurizio Ponz de Leon
exaly   +4 more sources

Muir-Torre-Syndrom

Der Chirurg, 2002
The Muir-Torre syndrome (MTS) is an autosomal dominant disease defined by the coincidence of at least one sebaceous skin tumor and one internal malignancy. We describe an additional case and give a review of the literature. Over a period of 7 years, 19 skin tumors were excised in a 50 year old male patient.
J, Jonas, R, Kruse, R, Bähr
  +6 more sources

Muir-Torre Syndrome

American Journal of Clinical Dermatology, 2007
In this case report of Muir-Torre syndrome (MTS), we describe a 47-year-old man with a personal and family history of colon cancer and a personal history of keratoacanthoma who presented with a sebaceous carcinoma and, subsequently, had a cystic sebaceous tumor.
Anne M, Lachiewicz   +4 more
openaire   +3 more sources

Muir-Torre Syndrome

Annals of Plastic Surgery, 1998
Muir-Torre syndrome is a rare autosomal dominant disorder characterized by unusual sebaceous neoplasms and visceral malignancy. Excluding sebaceous hyperplasia and sebaceous nevus of Jadassohn, sebaceous neoplasms occur so rarely that the presence of a sebaceous neoplasm mandates consideration of Muir-Torre syndrome.
P J, Johnson, F, Heckler
openaire   +2 more sources

Muir-Torre syndrome

Revista Clínica Española (English Edition), 2019
Muir-Torre syndrome (MTS) is an autosomal dominant disease with approximately 200 reported cases worldwide, which is characterised by multiple neoplasms of the skin and internal organs. This is a case report of a 57-year-old woman with MTS, who was referred to a plastic surgery department from a gastroenterology department due to a neoplasm of the skin.
M, Garayar Cantero   +2 more
openaire   +4 more sources

Muir-Torre syndrome

European Journal of Plastic Surgery, 2004
Muir–Torre syndrome is a rare autosomal dominant disorder characterized by sebaceous neoplasms of skin and one or more malignancies of the visceral organs. The sebaceous neoplasms include sebaceous adenoma, sebaceous epithelioma, basal cell epithelioma, and sebaceous carcinoma [1]. Since these sebaceous neoplasms occur rarely, when they are recognized,
Alper Tuncel   +2 more
openaire   +2 more sources

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