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Muir-Torre Syndrome

2013
Muir-Torre syndrome (MTS) is a rare, autosomal dominant genodermatosis characterized by sebaceous neoplasms, keratoacanthomas, and visceral malignancies [1, 2]. MTS is a phenotypic subset of hereditary nonpolyposis colorectal cancer (HNPCC) caused by mutations in mismatch repair genes associated with microsatellite instability [3]. Due to the increased
Adam J. Luber, Joshua A. Zeichner
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[Muir-Torre syndrome].

Orvosi hetilap, 1999
Muir-Torre syndrome patients have multiple visceral malignancies along with cutaneous sebaceous tumors and keratoacanthomas. We describe a history of a 64-year-old male patient with 13 tumours, who survived 13 years. The initial ascending colon adenocarcinoma was followed by some different tumors of the skin: adenoma and carcinoma of sebaceous glands ...
L, Tiszlavicz, Z, Hódi, Z, Tihanyi
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Neuromalignancy complicating the Muir–Torre syndrome

Journal of Cutaneous Pathology, 2015
Keywords: brain cancer; hereditary nonpolyposis colorectal cancer; immunohistochemistry; Muir–Torre syndrome; sebaceous ...
Drew J B, Kurtzman   +3 more
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Muir-Torre Syndrome: A Case Report

Tumori Journal, 1991
The authors present a case of Muir-Torre syndrome, the « sporadic » form, with a review of the literature. The importance of the close scrutiny of these patients and their relatives is stressed.
M, Bisceglia, P, Zenarola
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Muir-Torre syndrome.

Journal of the Royal College of Surgeons of Edinburgh, 2001
Muir-Torre syndrome is a rare autosomal dominant condition in which multiple primary malignancies occur together with a sebaceous gland tumour. Early recognition of the syndrome in patients with sebaceous gland tumours should facilitate early detection of subsequent malignancies if the patient with entered into appropriate screening programmes.
J, Coldron, I, Reid
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Sebaceous Neoplasms in Muir-Torre Syndrome

The American Journal of Dermatopathology, 2000
A 59-year-old Japanese woman presented with two sebaceous neoplasms on the chest wall and on the left cheek. The patient had a history of ascending colon cancer, and her mother had died of gastric cancer. The histopathologic features of both sebaceous neoplasms were vaguely in accordance with those of sebaceous adenoma and sebaceoma.
N, Misago, Y, Narisawa
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[Muir-Torre syndrome].

Nihon rinsho. Japanese journal of clinical medicine, 1996
Muir-Torre syndrome (MTS) is an autosomal dominant genodermatosis that is characterized by the presence of at least one sebaceous gland tumor with or without keratoacanthoma, and a minimum of one internal malignancy. The most commonly associated neoplasms were colorectal (51%) and genitourinary (25%).
R, Yoshikawa, J, Utsunomiya
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Muir-Torre syndrome: Facts and controversies

Clinics in Dermatology, 2010
The cutaneous presentation of a tumor sometimes has implications for a patient and his or her family, and Muir-Torre syndrome is an example of this. Because a single skin lesion can have broad consequences, it is important for clinicians to be aware of Muir-Torre syndrome.
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Muir-Torre-Syndrom

Der Hautarzt, 1995
Christine Hartig   +2 more
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Muir-Torre syndrome

2009
Frank Gaillard   +2 more
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