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  1. Occurrence of thyroid carcinoma in Dutch patients with familial adenomatous polyposis. An epidemiological study and report of new cases.

    Article - En anglais

    Objectives To assess the occurrence of thyroid cancer in Dutch patients with familial adenomatous polyposis (FAP) and to discuss the value of surveillance.

    Design Retrospective analysis of medical records.

    Setting The data were collected from the Dutch FAP registry.

    Participants 601 patients with FAP, 339 males and 262 females.

    Results The registry contained four female cases with a thyroid carcinoma.

    The mean age at diagnosis was 30 years (range : 16-46).

    In two patients it was the presenting symptom of FAP.

    None of the women died from their thyroid carcinoma during a mean follow-up of 13 years (range : 6-31).

    The histology revealed one papillary carcinoma, one follicular carcinoma and two mixed papillary/follicular carcinomas.

    The relative risk (RR) of developing thyroid carcinoma compared with the general Dutch population was 23 (95% confidence interval : 9-61).

    At the age of 60 years, the cumulative risk (CR) of thyroid carcinoma for female FAP patients was 2.8%. Conclusions Young female FAP patients have a significantly increased RR to develop a thyroid carcinoma.

    It may even be the presenting symptom of FAP.

    As the CR of thyroid carcinoma is low and the prognosis seems to be good, we recommend only periodical physical examination of the thyroid.

    Mots-clés Pascal : Carcinome, Thyroïde, Complication, Polypose rectocolique familiale, Epidémiologie, Prévalence, Surveillance, Evaluation, Fréquence apparition, Allemand, Homme, Tumeur maligne, Endocrinopathie, Thyroïde pathologie, Appareil digestif pathologie, Hérédité, Côlon pathologie

    Mots-clés Pascal anglais : Carcinoma, Thyroid gland, Complication, Familial adenomatous polyposis coli, Epidemiology, Prevalence, Surveillance, Evaluation, Occurrence frequency, German, Human, Malignant tumor, Endocrinopathy, Thyroid diseases, Digestive diseases, Inheritance(genetics), Colonic disease

    Logo du centre Notice produite par :
    Inist-CNRS - Institut de l'Information Scientifique et Technique

    Cote : 99-0001327

    Code Inist : 002B21C02. Création : 31/05/1999.

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