Literature DB >> 20664237

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

Nejat Isik1, Ilhan Elmaci, Bekir Gokben, Naci Balak, Nadir Tosyali.   

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. (c) 2010 S. Karger AG, Basel.

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Year:  2010        PMID: 20664237     DOI: 10.1159/000319007

Source DB:  PubMed          Journal:  Pediatr Neurosurg        ISSN: 1016-2291            Impact factor:   1.162


  7 in total

1.  Currarino syndrome: report of five consecutive patients.

Authors:  Soner Duru; Hakan Karabagli; Erhan Turkoglu; Yusuf Erşahin
Journal:  Childs Nerv Syst       Date:  2013-09-08       Impact factor: 1.475

2.  Concurrent Hirschsprung's disease and anorectal malformation: a systematic review.

Authors:  Hiroki Nakamura; Prem Puri
Journal:  Pediatr Surg Int       Date:  2019-09-24       Impact factor: 1.827

3.  Currarino triad with Müllerian duct anomaly in mother and daughter without MNX1 gene mutation.

Authors:  Soo-Hong Kim; Se Hyun Paek; Hyun-Young Kim; Sung-Eun Jung; Kwi-Won Park
Journal:  Ann Surg Treat Res       Date:  2015-12-29       Impact factor: 1.859

Review 4.  Association of Hirschsprung's disease and anorectal malformation: a systematic review.

Authors:  Alejandro D Hofmann; Prem Puri
Journal:  Pediatr Surg Int       Date:  2013-09       Impact factor: 1.827

5.  "This bicycle gives me a headache", a congenital anomaly.

Authors:  Hendt P Versteegh; Wout F J Feitz; Erik J van Lindert; Carlo Marcelis; Ivo de Blaauw
Journal:  BMC Res Notes       Date:  2013-10-14

6.  Currarino syndrome in an adult presenting with a presacral abscess: a case report.

Authors:  Masatoshi Shoji; Naomi Nojima; Akemi Yoshikawa; Wataru Fukushima; Naotaka Kadoya; Hisashi Hirosawa; Ryohei Izumi
Journal:  J Med Case Rep       Date:  2014-02-27

7.  Neurosurgical management of Currarino syndrome: A case series and review of literature.

Authors:  Alexander M Tucker; Peter Morgenstern; Daniel Diaz; Shaina Sedighim; Donald Shaul; Roman Sydorak; Mark Fedor; Amy Lee; Jason Hauptman
Journal:  Surg Neurol Int       Date:  2019-04-24
  7 in total

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