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    • Numéro 54 (Novembre 2025)
    Journal StorlJournal Storl
    Home»Numéro 48 ORIGINAL ARTICLE eng»BRAF V600E MUTATION IN DIFFERENTIATED THYROID CARCINOMA
    Numéro 48 ORIGINAL ARTICLE eng

    BRAF V600E MUTATION IN DIFFERENTIATED THYROID CARCINOMA

    MUTATION BRAF V600E DANS LE CANCER DIFFÉRENCIÉ DE LA THYROÏDE

    O. Trabelsi Grati 1, I. Achour 2, S. Charfi 3, A. Chakroun 2, J. Jdidi 5, S. Hugonin 4, R. Lacave 4,
    I. Charfeddine 2, T. Rebai 1, T. Sellami Boudawara 3, N. Bouayed Abdelmoula 1.
    1.Laboratory of Histology, Medicine school of Sfax. Tunisia
    2.Department of Otorhinolaryngology. Habib Bourguiba Teaching Hospital.
    3.Department of pathology. Habib Bourguiba Teaching Hospital, Sfax Tunisia
    4.Laboratory of Tumoral biology. Tenon Hospital, Paris. France
    5.Department of Epidemiology. Hedi Chaker Teaching Hospital, Sfax. Tunisia

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    Abstract

    Background: The BRAFV600E mutation is a common genetic alteration in papillary thyroid carcinoma (PTC). This mutation has been widely reported, more recentely, in north African population.
    Our objectives were to determine the prevalence of BRAF V600E in a Tunisian population with differentiated thyroid carcinoma and to investigate its association with aggressive clinicopathologic characteristics.
    Methods: DNA was extracted from paraffin-embedded thyroid tumor specimens taken from 13 patients with PTC and 7 patients with follicular carcinoma. BRAF V600E mutation was determined using multiplex real-time polymerase chain reaction (PCR) assay based on the TaqMan MGB probe system. The fluorescence absorbance of probes was calculated separately.
    Results: The BRAF mutation was present in 7 of 13 PTC (53,8%) but was not detected in follicular carcinoma. The age distribution, tumor size, multifocality, lymph node metastasis and staging did not differ significantly between patients with and without the BRAF(V600E) mutation.
    Conclusion: The BRAF V600E mutation was detected in more than half Tunisian patients with PTC which in accordance with the literature. However, its presence was not significantly associated with poor prognostic factors. Our findings need confirmation by large Tunisian and African series.
    Keywords: Tunisia, prognosis, genetic markers, DNA mutational analysis, carcinoma, papillary.

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    Article précédentCORRÉLATION ÉCHOGRAPHIE CERVICALE-SCINTIGRAPHIE PARATHYROÏDIENNE DANS L’HYPERPARATHYROÏDIEPRIMAIRE
    Article suivant OUTCOMES OF CHOANAL ATRESIA TRANSNASAL REPAIR: FACTORS RELATED TO RESTENOSIS

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    La société tunisienne d'ORL (STORL) a été crée le 8 avril 1981 grâce à la volonté et au courage de nos maîtres les professeurs M. Atallah, A. Belkahia, M. Bouraoui, H. Bouzouita, R. Ellouze, M. Fayala, A. Zaouche, et les regrettés professeurs M. Fourati et H. Sioud. Lire plus

    ACTUALITÉS
    MYOEPITHELIAL CARCINOMA OF THE SUBMANDIBULAR GLAND: A RARE CASE WITH LUNG METASTASIS
    SIALOLIPOME PAROTIDIEN: RAPORT D’UN CAS CLINIQUE
    SURGICAL TREATMENT OF THYROID NODULES IN CHILDREN
    PAPILLOME INVERSÉ NASO-SINUSIEN: INTÉRÊT DE L’IMAGERIE
    LES STENOSES LARYNGO-TRACHEALES EN ORL DU CHU SYLVANUS OLYMPIO DE LOME

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