The authors study the anomalies of the cranio-vertebral junction in the Morquio disease. The first 6 cases reported, in addition to the usual vertebral anomalies, suffered from a junctionnal malformations that were operated by posterior decompression and occipito-vertebral arthrodesis. In these cases, they especially study: --the neurological repercussion in 5 cases that could only be evidenced by a very careful examination after a stress test; --the simple roentgenographic examination, in forced position, and gaseous myelography proved on one band, that the instability, which is supposed to be responsible for the neurological symptoms, is actually inconstant (2 case out of 6). But on the other hand a narrow canal was present in every cases; --the surgical procedure performed in the 6 cases consisted of a removal of the posterior arch of the Atlas, of a widening of the occipital foramen if necessary (4 cases) and of an occipito-vertebral arthrodesis. There has been no aggravation compared to the previous state. Three indisputable improvements in the cases with a pyramidal syndrome. The authors compared their cases to those published in the literature and on which most of the time only a simple stabilisation was performed. For the authors this stabilisation can only be considered as a complementary procedure to the decompression which remains the main part of the treatment. The indications are discussed: they are based on the neurological examination and the myelography.
Download full-text PDF |
Source |
---|
Front Surg
December 2023
Neurosurgery & Pediatrics, University of Iowa Hospitals & Clinics, University of Iowa Stead Family Children's Hospital, Iowa City, IA, United States.
Introduction: Since the first description of os odontoideum in 1886, its origin has been debated. Numerous case series and reports show both a possible congenital origin and origin from the secondary to craniovertebral junction (CVJ) trauma. We conducted a detailed analysis of 260 surgically treated cases to document the initial symptoms, age groups, radiographic findings, and associated abnormalities, aiming to enhance the confirmation of the etiology.
View Article and Find Full Text PDFSurg Neurol Int
November 2023
Department of Orthopaedics, Seth Gordhandas Sunderdas Medical College and King Edward Memorial Hospital, Mumbai, Maharashtra, India.
Background: Craniovertebral junction (CVJ) pathologies include atlantoaxial instability/deformities resulting in myelopathy, respiratory failure, and even death. Here, we describe the indications, preoperative planning, and intra-operative/postoperative complications following surgical management of CVJ anomalies.
Methods: A prospective analysis of 34 patients with CVJ pathology was evaluated between 2015 and 2022.
Childs Nerv Syst
May 2023
Faculty of Medicine Department of Neurosurgery Division of Pediatric Neurosurgery, Gazi University, 06560, Ankara, Turkey.
Patients with mucopolysaccharidosis type IVA (MPS IVA) have many risk factors for myelopathy and paresis. These are spinal cord compression, bone stenosis, and soft tissue thickening with ligament laxity, deformity, odontoid hypoplasia, and atlantoaxial instability. Although most patients with MPS IVA appear generally healthy at birth, patients often show skeletal deformities within a few years.
View Article and Find Full Text PDFChilds Nerv Syst
August 2021
Department of Neurosurgery, Great Ormond Street Hospital, UCL Great Ormond Street Institute of Child Health, London, UK.
Purpose: Instability of the craniocervical junction in paediatric patients with skeletal dysplasia poses a unique set of challenges including anatomical abnormalities, poor bone quality, skeletal immaturity and associated general anaesthetic risks. Instrumented fixation provides optimal stabilisation and fusion rates. The small vertebrae make the placement of C2 pedicle screws technically demanding with low margins of error between the spinal canal and the vertebral artery.
View Article and Find Full Text PDFJ Craniovertebr Junction Spine
August 2020
Department of Neurosurgery, Sanjay Gandhi Post Graduate Institute of Medical Sciences, Lucknow, Uttar Pradesh, India.
Morquio syndrome (MS) is an autosomal recessive defect caused by the deficiency of N-acetylgalactosamine-6-sulfatase. Odontoid hypoplasia, periodontoid soft tissue deposition, and cervical stenosis lead to myelopathy and quadriparesis in these patients. Craniovertebral junction instability in MS possesses a surgical challenge as bones are yet to completely ossify.
View Article and Find Full Text PDFEnter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!