Mikosch P, Gallowitsch H J, Kresnik E, Lind P
Abteilung für Nuklearmedizin und spezielle Endokrinologie, Landeskrankenhaus Klagenfurt, Osterreich.
Nuklearmedizin. 1999;38(1):35-7.
A case of Graves' disease occurring in a patient with hemiagenesis is presented. The detection of the rare occurrence of a congenital hemiagenesis is often made by either clinical symptoms of thyroid dysfunction or anatomical abnormalities such as nodular goiter. The symptoms of hyperthyroidism in the current case led to the diagnostic confirmation by scintiscanning and ultrasonography of an absent lobe. Anti-thyroid antibody studies documented the presence of Graves' disease within the remaining lobe.
本文报告1例发生于半侧甲状腺缺如患者的格雷夫斯病。先天性半侧甲状腺缺如这种罕见情况的发现通常是通过甲状腺功能障碍的临床症状或解剖学异常,如结节性甲状腺肿。本例甲状腺功能亢进症状通过闪烁扫描和超声检查证实一侧叶缺如,从而确诊。抗甲状腺抗体研究证明在剩余叶内存在格雷夫斯病。