Pregled bibliografske jedinice broj: 64943
Muir-Torre syndrome: case report
Muir-Torre syndrome: case report // Journal of the European Academy of Dermatology and Venereology / Lotti, T ; Freedman, D. (ur.).
Oxford: Wiley-Blackwell, 2000. (poster, međunarodna recenzija, sažetak, znanstveni)
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Naslov
Muir-Torre syndrome: case report
Autori
Pašić, Aida ; Lončarić, Davorin ; Lipozenčić, Jasna, Čeović, Romana
Vrsta, podvrsta i kategorija rada
Sažeci sa skupova, sažetak, znanstveni
Izvornik
Journal of the European Academy of Dermatology and Venereology
/ Lotti, T ; Freedman, D. - Oxford : Wiley-Blackwell, 2000
Skup
9th Congress of the European Academy of Dermatology and Venereology
Mjesto i datum
Ženeva, Švicarska, 11.10.2000. - 15.10.2000
Vrsta sudjelovanja
Poster
Vrsta recenzije
Međunarodna recenzija
Ključne riječi
visceral carcinomas; sebaceous neoplasms; Muir-Torre disease
Sažetak
Muir-Torre syndrome (Muir, 1967, Torre, 1968) is a rare, autosomal dominantly inherited disorder defined by the occurrence of multiple visceral carcinomas and different types of sebaceous neoplasms. Visceral neoplasms have a relatively good prognosis. Sebaceous tumors may precede or follow the occurrence of visceral malignancy.
We present 68-year-old male patient with nodular tumour on the neck, showing a typical histologic picture of sebaceoma. His medical history included carcinoma of the testis at the age of 52 and colorectal carcinoma at the age of 65. His brother also had colorectal carcinoma at the age of 51.
Sebaceal neoplasms are very rare evants and each finding raises suspicion of Muir-Torre syndrome. Thorough history data are therefore very important and family members should be examined for possible occurrence of visceral carcinoma which is usually colorectal.
Izvorni jezik
Engleski
Znanstvena područja
Kliničke medicinske znanosti