Berdelou Amandine, Hartl Dana, Al Ghuzlan Abir, Mirghani Haïtham, Chougnet Cécile, Baudin Eric, Schlumberger Martin, Leboulleux Sophie
Institut Gustave-Roussy, Département de Médecine Nucléaire et d'Endocrinologie Oncologique, Faculté de Médecine Paris-Sud, 39 rue Camille-Desmoulins, 94805 Villejuif cedex, France.
Bull Cancer. 2013 Jul-Aug;100(7-8):780-8. doi: 10.1684/bdc.2013.1775.
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.
甲状腺髓样癌(MTC)在儿童中较为罕见。MTC几乎总是遗传性的,作为2A和2B型多发性内分泌肿瘤的一部分出现,这是由于RET原癌基因的种系突变所致。儿科人群中的MTC最常在家族基因调查过程中被诊断出来。但当孩子是先证者时,最常发现的是新发突变。主要目标是在甲状腺外扩展发生之前治疗MTC,因为当出现远处转移时,很少能治愈。治疗基于全甲状腺切除术加颈部淋巴结清扫术。