Karri Susmita Reddy, Roy Priya Susan, Nandi Nirjhar, Shenoy Vasant, Watson David
Department of Endocrinology, Townsville University Hospital, Douglas, Australia.
Genetic Pathology, Pathology Queensland, Brisbane, Australia.
Obstet Med. 2024 Jun;17(2):108-111. doi: 10.1177/1753495X221146340. Epub 2022 Dec 19.
Maternal Graves' autoantibodies are well known to cause fetal and neonatal thyroid disturbances. Despite radioiodine therapy, Graves' autoantibodies are known to persist, which can cross the placenta and cause hyperthyroidism in the fetus. We present the case of a 26-year-old woman in her first pregnancy, clinically and biochemically euthyroid with history of treated Graves' disease, where the fetus showed signs of hyperthyroidism on antenatal scans. This was confirmed by amniotic fluid testing as fetal blood sampling was not feasible and successfully treated with maternal carbimazole whilst continuing thyroxine for the mother (block-replacement). We discuss the challenges in the diagnosis of fetal hyperthyroidism and treatment whilst maternal thyroid status is maintained on thyroxine.
众所周知,母体的格雷夫斯病自身抗体会导致胎儿和新生儿甲状腺功能紊乱。尽管进行了放射性碘治疗,但格雷夫斯病自身抗体仍会持续存在,它可以穿过胎盘并导致胎儿甲状腺功能亢进。我们报告了一例26岁初孕妇的病例,该孕妇临床和生化检查甲状腺功能正常,有格雷夫斯病治疗史,其胎儿在产前超声检查中显示出甲状腺功能亢进的迹象。由于无法进行胎儿血样采集,通过羊水检测确诊,并在母亲继续服用甲状腺素(阻断替代疗法)的同时,成功地用母体服用的卡比马唑对胎儿进行了治疗。我们讨论了在维持母亲甲状腺素状态的同时诊断和治疗胎儿甲状腺功能亢进所面临的挑战。