Greening W P, Sarker S K, Osborne M P
Br J Surg. 1980 Jun;67(6):446-8. doi: 10.1002/bjs.1800670621.
Three cases of hemiagenesis of the thyroid gland are reported and the literature reviewed. It is emphasized that this rare congenital anomaly is seldom diagnosed except by thyroid scanning or at surgery. If the clinician is aware of it, the diagnosis presents little difficulty and an unnecessary operation may be avoided. All our cases were discovered as a result of an associated thyroid disorder. In 2 cases there was an adenoma and in 1 a papillary adenocarcinoma.
报告了3例甲状腺半侧发育不全病例,并对相关文献进行了综述。需要强调的是,这种罕见的先天性异常很少能被诊断出来,除非通过甲状腺扫描或手术。如果临床医生对此有所了解,诊断并不困难,且可避免不必要的手术。我们所有的病例都是由于相关的甲状腺疾病而被发现的。其中2例伴有腺瘤,1例伴有乳头状腺癌。