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Multiple primary melanomas.
Stam-Posthuma, J J; van Duinen, C; Scheffer, E; Vink, J; Bergman, W.
Afiliação
  • Stam-Posthuma JJ; Department of Dermatology and Pathology, Leiden University Medical Center, The Netherlands.
J Am Acad Dermatol ; 44(1): 22-7, 2001 Jan.
Article em En | MEDLINE | ID: mdl-11148472
ABSTRACT

BACKGROUND:

Patients with clinically diagnosed dysplastic nevi or a family history of melanoma with or without histologically diagnosed dysplastic nevi seem to be at higher risk for the development of multiple melanomas.

OBJECTIVE:

Our purpose was to determine which factors increased the risk for the development of subsequent melanomas.

METHODS:

This was a retrospective study in 56 patients with 157 melanomas.

RESULTS:

Early age at onset (58.9%), clinically diagnosed dysplastic nevi (82.0%), a histologically diagnosed dysplastic nevus (64%), family history of clinically diagnosed dysplastic nevi (70.8%) or melanoma (64.7%) and a histologically diagnosed dysplastic nevus in combination with a family history of melanoma (48%) were found in a high percentage of patients. The mean age at diagnosis was 38.2 years. The mean interval between the first and second melanoma was 34.3 months. Of the second melanomas, 76.8% developed in a different anatomic region from the first melanomas. The mean tumor thickness (Breslow) decreased from 1.11 mm for the first melanomas to 0.90 mm for the second melanomas.

CONCLUSION:

The results suggest that genetic factors might be involved in a certain subset of patients in whom melanomas develop early and successively.
Assuntos
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Base de dados: MEDLINE Assunto principal: Neoplasias Cutâneas / Síndrome do Nevo Displásico / Melanoma Idioma: En Ano de publicação: 2001 Tipo de documento: Article
Buscar no Google
Base de dados: MEDLINE Assunto principal: Neoplasias Cutâneas / Síndrome do Nevo Displásico / Melanoma Idioma: En Ano de publicação: 2001 Tipo de documento: Article