Literature DB >> 16432688

[Rare pathological alterations of the upper cervical spine requiring surgical treatment].

U Weber1, Y Robinson, R Kayser.   

Abstract

Because of its unique anatomy, specific diseases and lesions arise in the upper cervical spine, which differ widely from the rest of the spine. During the last two decades standardised diagnostic and therapeutic algorithms have been defined for most of the craniocervical pathologies often occurring in combination with an underlying disease requiring surgical intervention as well. On the other hand there are some very rare phathological alterations: about 20% of the patients suffering from neurofibromatosis type I develop spinal deformities. These are mostly found in the thoracic and lumbar spine (dystrophic/non-dystrophic type). In rare cases the dystrophic neurofibromatosis type I involves the upper cervical spine leading to bizarre deformities endangering the spinal cord. An aggressive, timely and combined operative therapy is necessary. Patients with Down syndrome should be investigated regularly for affections of the upper cervical spine. Though only in about 1% of all patients with Down syndrome do instabilities require surgical intervention, the upper cervical spine should be screened on a regular basis, since neurological changes due to the pathognomy of the underlying disease often remain undetected for a long time. The operative therapy of the instable os odontoideum in Down syndrome follows the general principles of this pathoanatomical variation. Even though the Klippel-Feil syndrome is generally not linked with neuropathological findings, rare associated deformities of the upper cervical spine should be excluded by proper diagnostic procedures.

Entities:  

Mesh:

Year:  2006        PMID: 16432688     DOI: 10.1007/s00132-005-0921-7

Source DB:  PubMed          Journal:  Orthopade        ISSN: 0085-4530            Impact factor:   1.087


  16 in total

Review 1.  Craniovertebral junction anomalies in inherited disorders: part of the syndrome or caused by the disorder?

Authors:  H A Crockard; J M Stevens
Journal:  Eur J Pediatr       Date:  1995-07       Impact factor: 3.183

2.  Klippel-Feil syndrome: CT and MR of acquired and congenital abnormalities of cervical spine and cord.

Authors:  J L Ulmer; A D Elster; L E Ginsberg; D W Williams
Journal:  J Comput Assist Tomogr       Date:  1993 Mar-Apr       Impact factor: 1.826

3.  Spine deformity in neurofibromatosis. A review of one hundred and two patients.

Authors:  R B Winter; J H Moe; D S Bradford; J E Lonstein; C V Pedras; A H Weber
Journal:  J Bone Joint Surg Am       Date:  1979-07       Impact factor: 5.284

4.  Cervical spine abnormalities in neurofibromatosis.

Authors:  K Yong-Hing; A Kalamchi; G D MacEwen
Journal:  J Bone Joint Surg Am       Date:  1979-07       Impact factor: 5.284

5.  Neurofibromatosis of the cervical spine. A report of eight cases.

Authors:  J B Craig; S Govender
Journal:  J Bone Joint Surg Br       Date:  1992-07

6.  Treatment of Down syndrome-associated craniovertebral junction abnormalities.

Authors:  D A Taggard; A H Menezes; T C Ryken
Journal:  J Neurosurg       Date:  2000-10       Impact factor: 5.115

Review 7.  Understanding the os odontoideum.

Authors:  E Forlin; D Herscovici; J R Bowen
Journal:  Orthop Rev       Date:  1992-12

8.  Craniovertebral abnormalities in Down's syndrome.

Authors:  A H Menezes; T C Ryken
Journal:  Pediatr Neurosurg       Date:  1992       Impact factor: 1.162

Review 9.  Neuroimaging features of neurenteric cysts: analysis of nine cases and review of the literature.

Authors:  B S Brooks; E R Duvall; T el Gammal; J H Garcia; K L Gupta; A Kapila
Journal:  AJNR Am J Neuroradiol       Date:  1993 May-Jun       Impact factor: 3.825

Review 10.  [Atlanto-axial dislocation in Down syndrome and os odontoieum. Case report and review of the literature].

Authors:  C Schmid; J Kittel
Journal:  Psychiatr Neurol Med Psychol (Leipz)       Date:  1988-08
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