Results 151 to 160 of about 3,333 (172)
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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 (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, 2010The 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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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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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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The Familial Muir-Torre Syndrome
Annals of Internal Medicine, 1993F P, Li, C, Eng
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Sebaceous neoplasia and the Muir–Torre syndrome: important connections with clinical implications
Histopathology, 2010Sara C Shalin, Alexander J Lazar
exaly