Literature DB >> 9309784

Posterior fossa decompression without duraplasty in infants and young children for treatment of Chiari malformation and achondroplasia.

K D Yundt1, T S Park, V S Tantuwaya, B A Kaufman.   

Abstract

Some children with Chiari malformation and achondroplasia require posterior fossa decompression that typically includes expansion of the dural tube with duraplasty. Infants and young children, however, may have a more distensible dura mater than do older patients. Furthermore, the structures that compress the hindbrain of young patients may be the bone and abnormally thickened atlantooccipital membrane, i.e., dural band, rather than the dura mater. We have treated 7 children who had Chiari malformation or achondroplasia with posterior fossa decompression without duraplasty. All children were symptomatic; 3 had Chiari-I malformations, 2 Chiari-II malformations, and 2 achondroplasia. The age range was 3 months to 2.5 years (mean 15.1 months). The exent of tonsillar herniation and other hindbrain anomalies was assessed on preoperative magnetic resonance imaging. The infants with Chiari-II malformations underwent cervical laminectomies, whereas the other young children with Chiari-I malformations or achondroplasia underwent suboccipital craniectomy as well as cervical laminectomy. In Chiari malformation, the dural band was divided; in achondroplasia, there was no identifiable dural band. Following bony decompression and division of the identifiable dural band, immediate expansion of the stenotic region with visible cerebrospinal fluid space posterior to the neural elements could be ascertained by intraoperative ultrasonography. During a follow-up period ranging from 4.5 months to 4 years (mean 22 months), all patients made improvements in their symptoms, 3 having complete resolution of their symptoms. This preliminary experience indicates that in children 2 years of age or younger, posterior fossa bony decompression without duraplasty can be effective treatment for Chiari malformations or achondroplasia.

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Year:  1996        PMID: 9309784     DOI: 10.1159/000121129

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


  6 in total

Review 1.  Pathogenesis of syringomyelia associated with Chiari type 1 malformation: review of evidences and proposal of a new hypothesis.

Authors:  Izumi Koyanagi; Kiyohiro Houkin
Journal:  Neurosurg Rev       Date:  2010-06-08       Impact factor: 3.042

2.  Bony decompression vs duraplasty for Chiari I malformation: does the eternal dilemma matter?

Authors:  Luca Massimi; P Frassanito; F Bianchi; G Tamburrini; M Caldarelli
Journal:  Childs Nerv Syst       Date:  2019-06-18       Impact factor: 1.475

3.  Chiari type 1 anomaly in pseudohypoparathyroidism type Ia: pathogenetic hypothesis.

Authors:  Juan F Martínez-Lage; Encarna Guillén-Navarro; Antonio L López-Guerrero; María José Almagro; Beatriz Cuartero-Pérez; Pedro de la Rosa
Journal:  Childs Nerv Syst       Date:  2011-10-13       Impact factor: 1.475

4.  Surgical management of symptomatic Chiari II malformation in infants and children.

Authors:  S Hassan A Akbari; David D Limbrick; David H Kim; Prithvi Narayan; Jeffrey R Leonard; Matthew D Smyth; Tae Sung Park
Journal:  Childs Nerv Syst       Date:  2013-02-07       Impact factor: 1.475

5.  Surgical management of patients with Chiari I malformation.

Authors:  John Siasios; Eftychia Z Kapsalaki; Kostas N Fountas
Journal:  Int J Pediatr       Date:  2012-06-28

6.  Intraoperative computed tomography for cervicomedullary decompression of foramen magnum stenosis in achondroplasia: two case reports.

Authors:  Hidetaka Arishima; Kenzo Tsunetoshi; Toshiaki Kodera; Ryuhei Kitai; Hiroaki Takeuchi; Ken-Ichiro Kikuta
Journal:  Neurol Med Chir (Tokyo)       Date:  2013-10-21       Impact factor: 1.742

  6 in total

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