Cancer médullaire de la thyroïde (CMT) de l'enfant

Translated title of the contribution: Medullary thyroid carcinoma in children

Amandine Berdelou, Dana Hartl, Abir Al Ghuzlan, Haïtham Mirghani, Cécile Chougnet, Éric Baudin, Martin Schlumberger, Sophie Leboulleux

    Research output: Contribution to journalArticlepeer-review

    3 Citations (Scopus)

    Abstract

    Medullary thyroid carcinoma (MTC) is rare in children. MTC is almost always inherited and occurs as part of a multiple endocrine neoplasia type 2A and B, due to germline mutation in the RET proto-oncogene. MTC in the pediatric population is most often diagnosed in the course of a familial genetic investigation. But when the child is the proband, a de novo mutation is most often founded. The main aim is to treat MTC before extrathyroidal extension occurs because when distant metastases are present, it is rarely curable. Treatment is based on total thyroidectomy with cervical lymph node dissection.

    Translated title of the contributionMedullary thyroid carcinoma in children
    Original languageFrench
    Pages (from-to)780-788
    Number of pages9
    JournalBulletin du Cancer
    Volume100
    Issue number7-8
    DOIs
    Publication statusPublished - 1 Jan 2013

    Cite this