Revision surgery for chiari malformation decompression

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Surgical treatment of craniocervical decompression without Chiari malformation in syringomyelia.

We aimed to describe a patient without Chiari malformation who was treated via craniocervical decompression and by creating cisterna manga with an autologous fascia graft, and who displayed a clinical and radiological improvement in the post-operative period. Syringomyelia is a chronic and progressive disease with cavitation and gliosis in the spinal cord. It is more common in adulthood and oft...

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Chiari I malformation with underlying pseudotumor cerebri: Poor symptom relief following posterior decompression surgery

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 Pseudotumor cerebri (PTC) patients exhibit clear clinical signs and symptoms of higher intracranial pressure (ICP) without ventricular enlargement or mass lesions. The clinical picture of patients with PTC can sometimes be similar to that of Chiari Malformation type I (CMI). There is some evidence that Chiari I malformation and PTC may coexist, which raises the question of whethe...

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Chiari malformation

Chiari malformation describes a group of structural defects of the cerebellum, characterized by brain tissue protruding into the spinal canal. Chiari malformations are often associated with myelomeningocele, hydrocephalus, syringomyelia, and tethered cord syndrome. Although studies of etiology are few, an increasing number of specific genetic syndromes are found to be associated with Chiari mal...

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Reasons for revision surgery after orbital decompression for Graves’ orbitopathy

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A 15 year old patient with a 6 month history of cough headache was diagnosed as having a Chiari I malformation. The midsagittal T1 weighted MRI shows the tonsillar ectopia (figure A). A flow sensitive MRI, cardiac triggered gradient echo T2* weighted sequence obtained at 200 ms from the R wave, showed absence of CSF flow through the foramen of Magendie (figure B). After craniovertebral decompre...

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ژورنال

عنوان ژورنال: Neurosurgical Focus

سال: 2003

ISSN: 1092-0684

DOI: 10.3171/foc.2003.15.3.3