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OEIS综合征:两例说明异常谱系的病例报告及文献综述

The OEIS complex: two case reports that illustrate the spectrum of abnormalities and a review of the literature.

作者信息

Vasudevan Pradeep C, Cohen Marta C, Whitby Elspeth H, Anumba Dilly O C, Quarrell Oliver W J

机构信息

Department of Clinical Genetics, Sheffield Children's Hospital, Sheffield, UK.

出版信息

Prenat Diagn. 2006 Mar;26(3):267-72. doi: 10.1002/pd.1394.

Abstract

We present two cases of OEIS (omphalocele, exstrophy, imperforate anus, spinal defects) complex -MIM 258040 and a review of the literature. Case 1 was a 14-year-old girl who presented at 30 weeks' gestation. An ultrasound examination showed an omphalocele and spina bifida; the bladder was not visualised. She went into spontaneous labour two weeks later and the baby died shortly after birth. A full post-mortem examination was refused, but the mother did agree to an external examination, skin biopsy for fibroblast culture, X rays and MR imaging. The MR imaging showed a pelvic kidney, a large omphalocele containing the other kidney, liver, bowel and a fluid filled structure thought to represent an exstrophy of the bladder (EB). Case 2 was a 30-year-old woman who had an ultrasound examination at 20 weeks' gestation; this showed an omphalocele, but the bladder was not visualised. The pregnancy was subsequently terminated and a post-mortem examination showed a low set umbilical cord associated with a small omphalocele; there was an imperforate anus; a blind ending rectum terminated in the omphalocele. We conclude that these two cases illustrate the variability of the OEIS complex.

摘要

我们报告两例OEIS(脐膨出、膀胱外翻、肛门闭锁、脊柱裂)综合征(MIM 258040)并对文献进行综述。病例1为一名14岁女孩,孕30周时就诊。超声检查显示脐膨出和脊柱裂;膀胱未显示。两周后她自然分娩,婴儿出生后不久死亡。家属拒绝了全面尸检,但母亲同意进行外部检查、皮肤活检以进行成纤维细胞培养、X线检查和磁共振成像。磁共振成像显示盆腔肾、一个包含另一个肾脏、肝脏、肠管以及一个被认为代表膀胱外翻(EB)的液性结构的大脐膨出。病例2为一名30岁女性,孕20周时进行超声检查;显示有脐膨出,但膀胱未显示。随后终止妊娠,尸检显示低位脐带伴小脐膨出;存在肛门闭锁;盲端直肠终止于脐膨出内。我们得出结论,这两例病例说明了OEIS综合征的变异性。

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