Complete caudal duplication syndrome

被引：1

作者：

Xing, Guodong ^{[1
]}

Huang, Liuming ^{[1
]}

Liu, Gang ^{[1
]}

Zhang, Jing ^{[1
]}

Xie, Huawei ^{[1
]}

Shen, Zhou ^{[1
]}

机构：

[1] Chinese Peoples Liberat Army Gen Hosp, Med Ctr 7, Bayi Childrens Hosp, Dept Pediat Surg, Beijing 100700, Peoples R China

来源：

JOURNAL OF PEDIATRIC SURGERY CASE REPORTS | 2020年 / 60卷

关键词：

Caudal duplication syndrome (CDS); Pelvic duplication; Lower limbs duplication;

D O I：

10.1016/j.epsc.2020.101543

中图分类号：

R72 [儿科学];

学科分类号：

100202 ;

摘要：

Caudal duplication syndrome (CDS) is associated with duplications involving the gastrointestinal, genitourinary, and spine/spinal cord. It is rare to encounter a single infant with all of the mentioned abnormalities, meanwhile, with duplex pelvis and both lower limbs. Here we firstly present a male infant with an omphalocele; bilateral cryptorchidism; congenital intestinal malrotation; spina bifida; duplex pelvis, lower limbs, penis, urogenital system, ileum, colon, rectum, anus, and blood vessels of pelvic. We call it complete caudal duplication syndrome. The first-stage of operation was performed and the 4-year follow-up showed no obvious growth and development restriction. It was planned to perform second-stage surgery.

引用

页数：5