{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,6,23]],"date-time":"2026-06-23T10:48:42Z","timestamp":1782211722352,"version":"3.54.5"},"reference-count":22,"publisher":"Journal of Neurosurgery Publishing Group (JNSPG)","issue":"1","content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":[],"published-print":{"date-parts":[[2005,1]]},"abstract":"<jats:p content-type=\"fine-print\">P In Type I split cord malformation (SCM) lesions, the osteocartilaginous spur and its dural sleeve are almost always located in the caudal extent of the median cleft. The authors present a case of lumbar myelomeningocele associated with a thoracic Type I SCM in which an osseous septum is uniquely situated in the proximal extent of the median cleft. Split cord malformations are cord-tethering lesions, which may be associated with a myelomeningocele that causes additional tethering, even in the opposite direction; therefore, both lesions should be treated. In view of this unique case, however, the surgical approach used for tethering lesions in such cases of complex spina bifida should perhaps be tailored. Whenever feasible, meticulous preoperative examination of a patient with spina bifida, including entire craniospinal magnetic resonance imaging followed with perioperative dynamic evaluation, is important for the effectiveness and safety of the surgery.<\/jats:p>","DOI":"10.3171\/ped.2005.102.1.0092","type":"journal-article","created":{"date-parts":[[2010,8,27]],"date-time":"2010-08-27T06:01:06Z","timestamp":1282888866000},"page":"92-95","source":"Crossref","is-referenced-by-count":0,"title":["Proximally situated osseous septum in complex spina bifida"],"prefix":"10.3171","volume":"102","author":[{"given":"G\u00fclsah","family":"Bademci","sequence":"first","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Cetin","family":"Evliyaoglu","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Semih","family":"Keskil","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]}],"member":"1754","reference":[{"key":"b1","series-title":"Pediatr Neurosurg","doi-asserted-by":"publisher","first-page":"225","DOI":"10.1159\/000058424","article-title":"Dorsal bony septum: a split cord malformation variant.","volume":"36","author":"Akay","year":"2002"},{"key":"b2","series-title":"Pediatr Neurosurg","doi-asserted-by":"publisher","first-page":"49","DOI":"10.1159\/000028831","article-title":"An unusual case of dorsally situated bony spur in a lumbar split cord malformation.","volume":"31","author":"Chandra","year":"1999"},{"key":"b3","series-title":"J Pathol","doi-asserted-by":"publisher","first-page":"83","DOI":"10.1002\/path.1711100110","article-title":"The local cord lesion in neurospinal dysraphism (meningomyelocele).","volume":"110","author":"Emery","year":"1973"},{"key":"b4","series-title":"Pediatr Neurosurg","doi-asserted-by":"publisher","first-page":"155","DOI":"10.1159\/000121033","article-title":"Split cord malformations: report of three unusual cases.","volume":"24","author":"Er\u015fahin","year":"1996"},{"key":"b5","series-title":"J Neurosurg","doi-asserted-by":"publisher","first-page":"57","DOI":"10.3171\/jns.1998.88.1.0057","article-title":"Split cord malformations in children.","volume":"88","author":"Er\u015fahin","year":"1998"},{"key":"b6","series-title":"Br J Neurosurg","doi-asserted-by":"publisher","first-page":"200","DOI":"10.1080\/026886900408360","article-title":"Split cord malformations in myelomeningocele patients.","volume":"14","author":"Iskandar","year":"2000"},{"key":"b7","series-title":"Pediatr Neurosurg","doi-asserted-by":"publisher","first-page":"119","DOI":"10.1159\/000048366","article-title":"Occurrence of split cord malformation in myelomeningocele: complex spina bifida.","volume":"36","author":"Kumar","year":"2002"},{"key":"b8","series-title":"Neurosurgery","doi-asserted-by":"publisher","first-page":"481","DOI":"10.1227\/00006123-199209000-00011","article-title":"Split cord malformation: Part II: Clinical syndrome.","volume":"31","author":"Pang","year":"1992"},{"key":"b9","series-title":"Neurosurgery","doi-asserted-by":"publisher","first-page":"451","DOI":"10.1227\/00006123-199209000-00010","article-title":"Split cord malformation: Part I: A unified theory of embryogenesis for double spinal cord malformations.","volume":"31","author":"Pang","year":"1992"},{"key":"b10","series-title":"Childs Nerv Syst","doi-asserted-by":"publisher","first-page":"48","DOI":"10.1007\/BF00573856","article-title":"Cervico-thoracic neurenteric cyst: clinicoradiological correlation with embryogenesis.","volume":"12","author":"Prasad","year":"1996"},{"key":"b11","series-title":"J Neurosurg","doi-asserted-by":"publisher","first-page":"709","DOI":"10.3171\/jns.1996.85.4.0709","article-title":"Dorsal midline proboscis associated with diastematomyelia and tethered cord syndrome. Case report.","volume":"85","author":"Yamada","year":"1996"},{"key":"b1","series-title":"Pediatr Neurosurg","doi-asserted-by":"publisher","first-page":"225","DOI":"10.1159\/000058424","article-title":"Dorsal bony septum: a split cord malformation variant.","volume":"36","author":"Akay","year":"2002"},{"key":"b2","series-title":"Pediatr Neurosurg","doi-asserted-by":"publisher","first-page":"49","DOI":"10.1159\/000028831","article-title":"An unusual case of dorsally situated bony spur in a lumbar split cord malformation.","volume":"31","author":"Chandra","year":"1999"},{"key":"b3","series-title":"J Pathol","doi-asserted-by":"publisher","first-page":"83","DOI":"10.1002\/path.1711100110","article-title":"The local cord lesion in neurospinal dysraphism (meningomyelocele).","volume":"110","author":"Emery","year":"1973"},{"key":"b4","series-title":"Pediatr Neurosurg","doi-asserted-by":"publisher","first-page":"155","DOI":"10.1159\/000121033","article-title":"Split cord malformations: report of three unusual cases.","volume":"24","author":"Er\u015fahin","year":"1996"},{"key":"b5","series-title":"J Neurosurg","doi-asserted-by":"publisher","first-page":"57","DOI":"10.3171\/jns.1998.88.1.0057","article-title":"Split cord malformations in children.","volume":"88","author":"Er\u015fahin","year":"1998"},{"key":"b6","series-title":"Br J Neurosurg","doi-asserted-by":"publisher","first-page":"200","DOI":"10.1080\/026886900408360","article-title":"Split cord malformations in myelomeningocele patients.","volume":"14","author":"Iskandar","year":"2000"},{"key":"b7","series-title":"Pediatr Neurosurg","doi-asserted-by":"publisher","first-page":"119","DOI":"10.1159\/000048366","article-title":"Occurrence of split cord malformation in myelomeningocele: complex spina bifida.","volume":"36","author":"Kumar","year":"2002"},{"key":"b8","series-title":"Neurosurgery","doi-asserted-by":"publisher","first-page":"481","DOI":"10.1227\/00006123-199209000-00011","article-title":"Split cord malformation: Part II: Clinical syndrome.","volume":"31","author":"Pang","year":"1992"},{"key":"b9","series-title":"Neurosurgery","doi-asserted-by":"publisher","first-page":"451","DOI":"10.1227\/00006123-199209000-00010","article-title":"Split cord malformation: Part I: A unified theory of embryogenesis for double spinal cord malformations.","volume":"31","author":"Pang","year":"1992"},{"key":"b10","series-title":"Childs Nerv Syst","doi-asserted-by":"publisher","first-page":"48","DOI":"10.1007\/BF00573856","article-title":"Cervico-thoracic neurenteric cyst: clinicoradiological correlation with embryogenesis.","volume":"12","author":"Prasad","year":"1996"},{"key":"b11","series-title":"J Neurosurg","doi-asserted-by":"publisher","first-page":"709","DOI":"10.3171\/jns.1996.85.4.0709","article-title":"Dorsal midline proboscis associated with diastematomyelia and tethered cord syndrome. Case report.","volume":"85","author":"Yamada","year":"1996"}],"container-title":["Journal of Neurosurgery: Pediatrics"],"original-title":[],"link":[{"URL":"https:\/\/thejns.org\/view\/journals\/j-neurosurg-pediatr\/102\/1\/article-p92.xml","content-type":"text\/html","content-version":"vor","intended-application":"text-mining"},{"URL":"https:\/\/thejns.org\/downloadpdf\/journals\/j-neurosurg-pediatr\/102\/1\/article-p92.xml","content-type":"text\/html","content-version":"vor","intended-application":"syndication"},{"URL":"https:\/\/thejns.org\/downloadpdf\/journals\/j-neurosurg-pediatr\/102\/1\/article-p92.xml","content-type":"unspecified","content-version":"vor","intended-application":"similarity-checking"}],"deposited":{"date-parts":[[2026,6,23]],"date-time":"2026-06-23T10:14:38Z","timestamp":1782209678000},"score":1,"resource":{"primary":{"URL":"https:\/\/thejns.org\/view\/journals\/j-neurosurg-pediatr\/102\/1\/article-p92.xml"}},"subtitle":["Case report"],"short-title":[],"issued":{"date-parts":[[2005,1]]},"references-count":22,"journal-issue":{"issue":"1"},"URL":"https:\/\/doi.org\/10.3171\/ped.2005.102.1.0092","relation":{},"ISSN":["0022-3085"],"issn-type":[{"value":"0022-3085","type":"print"}],"subject":[],"published":{"date-parts":[[2005,1]]}}}