Literature DB >> 15081131

Imaging in spine and spinal cord malformations.

Andrea Rossi1, Roberta Biancheri, Armando Cama, Gianluca Piatelli, Marcello Ravegnani, Paolo Tortori-Donati.   

Abstract

Spinal and spinal cord malformations are collectively named spinal dysraphisms. They arise from defects occurring in the early embryological stages of gastrulation (weeks 2-3), primary neurulation (weeks 3-4), and secondary neurulation (weeks 5-6). Spinal dysraphisms are categorized into open spinal dysraphisms (OSDs), in which there is exposure of abnormal nervous tissues through a skin defect, and closed spinal dysraphisms (CSD), in which there is a continuous skin coverage to the underlying malformation. Open spinal dysraphisms basically include myelomeningocele and other rare abnormalities such as myelocele and hemimyelo(meningo)cele. Closed spinal dysraphisms are further categorized based on the association with low-back subcutaneous masses. Closed spinal dysraphisms with mass are represented by lipomyelocele, lipomyelomeningocele, meningocele, and myelocystocele. Closed spinal dysraphisms without mass comprise simple dysraphic states (tight filum terminale, filar and intradural lipomas, persistent terminal ventricle, and dermal sinuses) and complex dysraphic states. The latter category further comprises defects of midline notochordal integration (basically represented by diastematomyelia) and defects of segmental notochordal formation (represented by caudal agenesis and spinal segmental dysgenesis). Magnetic resonance imaging (MRI) is the preferred modality for imaging these complex abnormalities. The use of the aforementioned classification scheme is greatly helpful to make the diagnosis.

Entities:  

Mesh:

Year:  2004        PMID: 15081131     DOI: 10.1016/j.ejrad.2003.10.015

Source DB:  PubMed          Journal:  Eur J Radiol        ISSN: 0720-048X            Impact factor:   3.528


  25 in total

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Authors:  Priyanka Jha; Soni C Chawla
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2.  Novel mutations in Lrp6 orthologs in mouse and human neural tube defects affect a highly dosage-sensitive Wnt non-canonical planar cell polarity pathway.

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Review 3.  [Spina bifida].

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4.  Contribution of VANGL2 mutations to isolated neural tube defects.

Authors:  Z Kibar; S Salem; C M Bosoi; E Pauwels; P De Marco; E Merello; A G Bassuk; V Capra; P Gros
Journal:  Clin Genet       Date:  2010-07-22       Impact factor: 4.438

5.  Feasibility and limitation of constructive interference in steady-state (CISS) MR imaging in neonates with lumbosacral myeloschisis.

Authors:  Kimiaki Hashiguchi; Takato Morioka; Fumiaki Yoshida; Yasushi Miyagi; Futoshi Mihara; Takashi Yoshiura; Shinji Nagata; Tomio Sasaki
Journal:  Neuroradiology       Date:  2007-03-31       Impact factor: 2.804

6.  A rare case of thoracic myelocystocele associated with type 1 split cord malformation with low lying tethered cord, dorsal syrinx and sacral agenesis: Pentad finding.

Authors:  Dipanker Singh Mankotia; Guru Dutta Satyarthee; Bhawani Shankar Sharma
Journal:  J Neurosci Rural Pract       Date:  2015-01

Review 7.  Imaging in congenital deformities of the spinal cord.

Authors:  G Guglielmi; S Utomo; M Cascavilla; P Rahardjo; R Setiawati; T Popolizio
Journal:  Radiol Med       Date:  2012-01-07       Impact factor: 3.469

Review 8.  Cervicothoracic cystic dysraphism.

Authors:  Natalie S Valeur; Ramesh S Iyer; Gisele E Ishak
Journal:  Pediatr Radiol       Date:  2016-05-05

9.  Malignant transformation of a lipomyelocele into a rhabdomyosarcoma?

Authors:  A M O'Connell; D Allcutt; F Brett; S Ryan
Journal:  AJNR Am J Neuroradiol       Date:  2008-01-09       Impact factor: 3.825

10.  Identification of new candidate genes for spina bifida through exome sequencing.

Authors:  Alessia Azzarà; Claudia Rendeli; Anna Maria Crivello; Fulvia Brugnoletti; Roberto Rumore; Emanuele Ausili; Eugenio Sangiorgi; Fiorella Gurrieri
Journal:  Childs Nerv Syst       Date:  2021-04-15       Impact factor: 1.475

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