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一名先天性甲状腺功能减退症婴儿,其母亲患有甲状腺功能减退症,体内存在未被诊断出的甲状腺刺激阻断抗体。

A baby with congenital hypothyroidism born to a hypothyroid mother who expressed undiagnosed thyroid stimulation blocking antibody.

作者信息

Kim Mock Ryeon, Park Hye Won, Chung Sochung

机构信息

Department of Pediatrics, Konkuk University Medical Center, Seoul, Korea.

Department of Pediatrics, Konkuk University Medical Center, Seoul, Korea.; Konkuk University School of Medicine, Seoul, Korea.

出版信息

Ann Pediatr Endocrinol Metab. 2016 Sep;21(3):161-163. doi: 10.6065/apem.2016.21.3.161. Epub 2016 Sep 30.

Abstract

In adults, hypothyroidism caused by thyroid stimulation blocking antibody (TSB Ab) is rare, and confirmed cases are even fewer, as TSB Ab levels are rarely assayed. However, this may create problems in babies, as the transplacental passage of maternal TSB Ab can cause a rare type of hypothyroidism in the infant. Prompt levothyroxine replacement for the baby starting immediately after birth is important. We describe a congenital hypothyroid baby born to a hypothyroid mother who was not aware of the cause of her hypothyroid condition, which turned out to be associated with the expression of TSB Ab. This cause was confirmed in both the infant and mother using a series of thyroid function tests and measurements of autoantibody levels, including TSB Ab. During periodic follow-up, the TSB Ab and thyroid stimulating hormone receptor antibody titers became negative in the baby at 8 months of age, but remained positive in the mother. Evaluation of hypothyroidism and its cause in mothers during pregnancy is important for both maternal and child health.

摘要

在成人中,由甲状腺刺激阻断抗体(TSB Ab)引起的甲状腺功能减退症很少见,而确诊病例更少,因为很少检测TSB Ab水平。然而,这可能会给婴儿带来问题,因为母体TSB Ab经胎盘传递可导致婴儿患一种罕见类型的甲状腺功能减退症。婴儿出生后立即开始及时补充左甲状腺素很重要。我们描述了一名先天性甲状腺功能减退的婴儿,其母亲患有甲状腺功能减退症,但她并不知道自己甲状腺功能减退的病因,结果发现这与TSB Ab的表达有关。通过一系列甲状腺功能测试和自身抗体水平测量,包括TSB Ab,在婴儿和母亲中均证实了这一病因。在定期随访期间,婴儿在8个月大时TSB Ab和促甲状腺激素受体抗体滴度变为阴性,但母亲的仍为阳性。孕期评估母亲甲状腺功能减退症及其病因对母婴健康都很重要。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e684/5073163/83d49da835aa/apem-21-161-g001.jpg

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