Weber Theresia
Department of Endocrine Surgery, Katholisches Klinikum, Mainz, Germany.
Visc Med. 2018 Dec;34(6):419-421. doi: 10.1159/000493809. Epub 2018 Nov 17.
Medullary thyroid carcinoma (MTC) represents a distinct form of thyroid cancer with a potentially aggressive behavior, early lymph node metastases, and sporadic as well as hereditary forms. Only surgery with total thyroidectomy and lymph node dissection is able to achieve biochemical cure. Due to the uncommon nature of MTC, a specialization in endocrine surgery for diagnosis as well as therapy of MTC seem to be mandatory for a successful treatment. Knowledge of genotype-phenotype correlations for hereditary forms or routine calcitonin screening for sporadic forms is important to analyze preoperative findings and plan surgical procedures. Postoperative follow-up depends on biochemical cure or monitoring for patients with elevated calcitonin levels.
甲状腺髓样癌(MTC)是一种特殊类型的甲状腺癌,具有潜在侵袭性、早期淋巴结转移的特点,有散发性和遗传性两种形式。只有行全甲状腺切除术及淋巴结清扫术才能实现生化治愈。由于MTC较为罕见,对于成功治疗而言,内分泌外科在MTC诊断及治疗方面的专业化似乎必不可少。了解遗传性MTC的基因型-表型相关性或对散发性MTC进行常规降钙素筛查,对于分析术前检查结果及规划手术方案很重要。术后随访取决于生化治愈情况或对降钙素水平升高患者的监测。