Respiratory arrest: a complication of cerebellar ectopia in adults.

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چکیده

منابع مشابه

Respiratory arrest: a complication of cerebellar ectopia in adults.

Two adult patients are described with cerebellar ectopia whose presentation at diagnosis was respiratory arrest. Following surgical decompression both patients become self ventilating and now lead independent lives. Cerebellar ectopia is a potentially remediable condition and should be considered in patients with unexplained respiratory arrest.

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Spinal intradural cerebellar ectopia.

An ectopic cerebellum, as in Chiari malformations and ectopic cerebellar dysplastic tissue, is a common finding; however, the presence of an organized ectopic cerebellum is exceedingly rare. We describe the MR imaging, surgical, and histologic appearance of an intraspinal ectopic cerebellum in an infant.

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Cerebellar ectopia presenting in adult life.

Three cases of cerebellar ectopia first producing symptoms in adult life are reported. This potentially remediable anomaly may not be suspected in adults, in whom associated congenital bony abnormalities of the skull and cervical spine are often absent. In these cases diagnosis depends on radiological contrast studies; in particular it is important to examine the cervical canal in the prone and...

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Denervation in wasted hand muscles in a case of primary cerebellar ectopia without syringomyelia.

Wasting of hand muscles and electromyographic changes of denervation in a case of primary cerebellar ectopia without evidence of syringomyelia is described. It is suggested that the wasting is due to anterior horn cell damage secondary to grey matter venous obstruction at high cervical cord levels.

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MR imaging of an extreme case of cerebellar ectopia in a patient with Chiari II malformation.

A 12-year-old boy who had been born with a meningomyelocele that was closed surgically 3 days after his birth had preoperative workup for a planned anterior release and posterior spinal instrumentation and fusion for worsening lumbosacral scoliosis. The patient had a history of developmental delay and learning disabilities and bowel and bladder incontinence. Physical examination showed thoracol...

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ژورنال

عنوان ژورنال: Journal of Neurology, Neurosurgery & Psychiatry

سال: 1988

ISSN: 0022-3050

DOI: 10.1136/jnnp.51.5.714