Malignancy associated genodermatoses
TURKDERM-ARCHIVES OF THE TURKISH DERMATOLOGY AND VENEROLOGY, cilt.47, ss.103-110, 2013 (SCI-Expanded, Scopus, TRDizin)
- Yayın Türü: Makale / Tam Makale
- Cilt numarası: 47
- Basım Tarihi: 2013
- Doi Numarası: 10.4274/turkderm.47.s18
- Dergi Adı: TURKDERM-ARCHIVES OF THE TURKISH DERMATOLOGY AND VENEROLOGY
- Derginin Tarandığı İndeksler: Science Citation Index Expanded (SCI-EXPANDED), Scopus, TR DİZİN (ULAKBİM)
- Sayfa Sayıları: ss.103-110
- Açık Arşiv Koleksiyonu: AVESİS Açık Erişim Koleksiyonu
- Hacettepe Üniversitesi Adresli: Hayır
Özet
The cutaneous features of some genetic diseases that manifest during childhood might be the first signs of predisposition to cancer; therefore, early recognition of such clinical findings as well as necessary follow-up are vital. This review focuses in particular on nevoid basal cell carcinoma, Cowden syndrome, neurofibromatosis type 1, tuberous sclerosis, Peutz-Jegher's syndrome, dyskeratosis congenita, and xeroderma pigmentosum. These genodermatoses, are characterised by predisposition to skin cancer or cancer in other organs; as such this review aimed to highlight their diagnostic clinical features.