Suppr超能文献

库拉里诺三联征:4例[应为3例]患者的手术治疗及随访结果

Currarino triad: surgical management and follow-up results of four [correction of three] cases.

作者信息

Isik Nejat, Elmaci Ilhan, Gokben Bekir, Balak Naci, Tosyali Nadir

机构信息

Department of Neurosurgery, Goztepe Research and Education Hospital, Istanbul, Turkey. nejatisik @ hotmail.com

出版信息

Pediatr Neurosurg. 2010 Aug;46(2):110-9. doi: 10.1159/000319007. Epub 2010 Jul 20.

Abstract

The Currarino syndrome is a rare triad that is a combination of a presacral mass, a congenital sacral bony abnormality and an anorectal malformation. We present 4 children with complete Currarino triad who were diagnosed using MRI. Our aim was to report the neurosurgical management of Currarino syndrome in children. All of the patients had chronic constipation and pain in the lumbosacral region. In the plain radiograph, 3 patients had a sacral scimitar-shaped bony abnormality, and 1 patient had total sacral agenesis. There was a narrow anal canal or narrow ventrally displaced anus in all patients. Their anorectal malformations were characterized as anal stenoses (4 patients), associated with Hirschsprung's disease in 2 cases. In 3 patients, MRI showed tethered cord syndrome in addition to the presacral mass. There was hydrocephalus in 1 patient. Anal stenosis was treated by anal dilatation. In 2 patients, rectal biopsy and temporary colostomy (2 patients) had been performed previously due to Hirschsprung's disease. We performed a posterior procedure via lumbar and sacral partial laminectomy-laminoplasty and transdural ligation of the neck of the meningocele for anterior sacral meningoceles, or alternatively, tumor excision for other types of presacral lesions. Histopathologically, 3 were cases of anterior sacral meningoceles and 1 was a teratoma. One of them also had a spinal abscess. He required reoperation (twice) and appeared at the time to have improved with medical therapy. All patients improved and stabilized. There were no additional neurological deficits and no recurrence of the presacral mass over the follow-up period (6 years, on average). The family pedigree did not reveal any familial transmission pattern. In cases of Currarino triad, MRI can allow the characterization of the presacral masses. If it is an anterior sacral meningocele or a solid tumor without severe anorectal malformation, it can be managed with posterior lumbar and sacral procedures. Such approaches are performed easily by transdural ligation of the neck of the anterior sacral meningocele or through tumor excision.

摘要

库拉里诺综合征是一种罕见的三联征,由骶前肿块、先天性骶骨骨质异常和肛门直肠畸形组成。我们报告4例经磁共振成像(MRI)诊断为完全性库拉里诺三联征的儿童病例。我们的目的是报道儿童库拉里诺综合征的神经外科治疗情况。所有患者均有慢性便秘和腰骶部疼痛。在X线平片中,3例患者有骶骨弯刀状骨质异常,1例患者骶骨完全缺如。所有患者均存在肛管狭窄或肛门腹侧移位狭窄。他们的肛门直肠畸形表现为肛门狭窄(4例),其中2例合并先天性巨结肠。3例患者MRI显示除骶前肿块外,还存在脊髓栓系综合征。1例患者有脑积水。肛门狭窄采用肛门扩张术治疗。2例患者因先天性巨结肠先前已行直肠活检和临时结肠造口术。对于骶前脊膜膨出,我们通过腰骶部部分椎板切除-椎板成形术及经硬膜结扎脊膜膨出颈部进行后路手术,对于其他类型的骶前病变则行肿瘤切除术。组织病理学检查显示,3例为骶前脊膜膨出,1例为畸胎瘤。其中1例还合并脊髓脓肿。他需要再次手术(两次),目前经药物治疗后病情有所改善。所有患者病情均有改善并稳定。随访期间(平均6年)无新增神经功能缺损,骶前肿块无复发。家族谱系未显示任何家族遗传模式。对于库拉里诺三联征病例,MRI可对骶前肿块进行特征性描述。如果是骶前脊膜膨出或无严重肛门直肠畸形的实体瘤,可采用腰骶部后路手术治疗。通过经硬膜结扎骶前脊膜膨出颈部或肿瘤切除等方法,此类手术操作简便。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验