
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. A case occurring in Scotland is described and implications for management, screening for members of the family are discussed.
Adult, Male, Carcinoma, Transitional Cell, Neoplasms, Second Primary, Syndrome, Adenocarcinoma, Kidney Neoplasms, Colonic Neoplasms, Humans, Kidney Pelvis, Sebaceous Gland Neoplasms
Adult, Male, Carcinoma, Transitional Cell, Neoplasms, Second Primary, Syndrome, Adenocarcinoma, Kidney Neoplasms, Colonic Neoplasms, Humans, Kidney Pelvis, Sebaceous Gland Neoplasms
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