The triad of bilateral retinoblastoma, dysplastic naevus syndrome and multiple cutaneous malignant melanomas: a case report and review of the literature


Autoria(s): Belt, P.J.; Smithers, M.; Elston, T.
Contribuinte(s)

P. A. Riley

G. Prota

F. J. Lejeune

Data(s)

01/04/2002

Resumo

We report a case of a patient with the triad of retinoblastoma, dysplastic naevus syndrome (DNS) and multiple cutaneous melanomas. The combination of retinoblastoma and DNS is a significant risk factor for the development of cutaneous melanoma. This risk extends to family members. We recommend that survivors of (inherited) retinoblastoma and their relatives are closely screened for the presence of dysplastic naevi. (C) 2002 Lippincott Williams Wilkins.

Identificador

http://espace.library.uq.edu.au/view/UQ:63457

Idioma(s)

eng

Publicador

Lippincott Williams & Wilkins, Ltd

Palavras-Chave #Oncology #Dermatology #Medicine, Research & Experimental #Melanoma #Retinoblastoma #Dysplastic Naevus Syndrome #Screening #2nd Tumors #Cancer #Relatives #Neoplasms #Survivors #Mortality #Children #Risk #C1 #110323 Surgery
Tipo

Journal Article