A case report of caudal regression syndrome associated with an intraspinal arachnoid cyst

被引:3
|
作者
Tsugu, H
Fukushima, T
Oshiro, S
Tomonaga, M
Utsunomiya, H
Oshima, K
Ohjimi, H
机构
[1] Fukuoka Univ, Sch Med, Dept Neurosurg, Jonan Ku, Fukuoka 8140180, Japan
[2] Fukuoka Univ, Sch Med, Dept Neuroradiol, Jonan Ku, Fukuoka 8140180, Japan
[3] Fukuoka Univ, Sch Med, Dept Urol, Jonan Ku, Fukuoka 8140180, Japan
[4] Fukuoka Univ, Sch Med, Dept Plast Surg, Jonan Ku, Fukuoka 8140180, Japan
关键词
caudal regression syndrome; sacral agenesis; imperforate anus; myelocystocele; spinal arachnoid cyst;
D O I
10.1159/000028863
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
We report here a rare case of caudal regression syndrome associated with an intraspinal arachnoid cyst, The patient was a 6-month-old baby girl with multicomplex congenital abnormalities: sacrococcygeal dysgenesis and ventral curvature, large terminal cyst (myelocystocele), spinal arachnoid cyst, cerebellar hypertrophy (suspected), high imperforate anus, partial dysgenesis of the large intestine, omphalocele, atresia of the vagina, bilateral incomplete ureter duplication, incomplete pseudo-duplicated bladder and bilateral talipes equinovarus. We performed plastic repair of the myelocystocele and perineal lesion for caudal regression syndrome and partial removal of the cyst wall for the intraspinal arachnoid cyst. She has been well for 3 years postoperatively, and her mental development is normal. Copyright (C) 2000 S. Karger AG, Basel.
引用
收藏
页码:207 / 212
页数:6
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