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直肠闭锁与先天性甲状腺功能减退症:一种关联还是巧合?

Rectal Atresia and Congenital Hypothyroidism: An Association or Coincidence?

作者信息

Mehmetoğlu Feride

机构信息

Department of Pediatric Surgery, Dortcelik Children's Hospital, Bursa, Turkey.

出版信息

European J Pediatr Surg Rep. 2018 Jan;6(1):e7-e10. doi: 10.1055/s-0037-1612610. Epub 2018 Jan 10.

Abstract

Rectal atresia is a rare anorectal malformation, and its association with other anomalies is even more rare. This study presents a unique case of co-twin in which the surviving newborn male underwent surgery due to rectal atresia. Newborn screening tests identified congenital hypothyroidism. The surgical treatment consisted of three stages and thyroid hormones were replaced.

摘要

直肠闭锁是一种罕见的肛肠畸形,其与其他异常情况并存则更为罕见。本研究报告了一例独特的联体双胎病例,其中存活的男婴因直肠闭锁接受了手术治疗。新生儿筛查发现先天性甲状腺功能减退。手术治疗分三个阶段进行,并给予甲状腺激素替代治疗。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6ae2/5762197/2409c96b8a77/10-1055-s-0037-1612610-i170353cr-1.jpg

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