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首页> 外文期刊>Pediatric neurosurgery >Currarino triad: surgical management and follow-up results of four (corrected) cases.
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Currarino triad: surgical management and follow-up results of four (corrected) cases.

机译:Currarino三联症:四例(矫正)病例的外科治疗和随访结果。

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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.
机译:Currarino综合征是一种罕见的三联征,是s前肿块,先天性s骨骨异常和肛门直肠畸形的组合。我们介绍了4名使用MRI诊断出的完全Currarino三联症患儿。我们的目的是报告儿童Currarino综合征的神经外科治疗。所有的患者在腰s部都有慢性便秘和疼痛。在X线平片中,有3名患者有sc骨弯刀形骨畸形,有1名患者完全total骨发育不全。所有患者均存在狭窄的肛门管或狭窄的腹侧移位肛门。他们的肛门直肠畸形的特征是肛门狭窄(4例),其中2例与Hirschsprung病有关。在3例患者中,MRI显示除s前肿块外还存在系绳综合征。 1例有脑积水。通过肛门扩张治疗肛门狭窄。在2例患者中,由于Hirschsprung病,曾进行了直肠活检和临时结肠造口术(2例)。我们通过腰椎和骨部分椎板切除术-椎板隆突术和脑膜后颈部硬膜结扎术进行了后路手术,以治疗前部脑膜膨出,或者通过肿瘤切除术治疗其他类型的s骨前病变。在组织病理学上,3骨前脑膜膨出3例,畸胎瘤1例。其中之一还患有脊髓脓肿。他需要再次手术(两次),并在当时似乎因药物治疗而有所改善。所有患者均改善并稳定。在随访期间(平均6年),没有其他神经功能缺损,s前肿块也没有复发。家谱没有显示任何家族传播方式。对于Currarino三联症,MRI可以表征s前肿块。如果是前部脑膜膨出或实体瘤而没有严重的肛门直肠畸形,则可以通过后路腰and部手术治疗。通过approaches骨前脑膜膨出颈颈部的硬脑膜结扎或通过肿瘤切除容易地进行这种方法。

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