A CASE OF ARNOLD-CHIARI TYPE-I MALFORMATION PRESENTING WITH DYSRHYTHMIC BREATHING DURING SLEEP
Citation
M. Miyamoto et al., A CASE OF ARNOLD-CHIARI TYPE-I MALFORMATION PRESENTING WITH DYSRHYTHMIC BREATHING DURING SLEEP, PSYCHIATRY AND CLINICAL NEUROSCIENCES, 52(2), 1998, pp. 212-216
Categorie Soggetti
Clinical Neurology",Neurosciences,Psychiatry
SICI code
1323-1316(1998)52:2<212:ACOATM>2.0.ZU;2-6
Abstract
A 43-year-old woman presented with dull headache, left tinnitus and di
zziness. Neurological examination revealed down-beat gaze nystagmus, l
eft tinnitus, positive Romberg sign, poor standing on the left foot, p
oor tandem gait, left spastic gait and positive pathological reflexes
in the bilateral upper and lower extremities. Plain X-ray of the skull
and cervical vertebrae demonstrated basilar impression and atlantoaxi
al fusion. Magnetic resonance imaging of the brain and cervical spine
showed cerebellar tonsil descent and syringomyelia located in the left
side of the spine at the II-III vertebral level which communicated wi
th the fourth ventricle. The patient was diagnosed as having cervical
syringomyelia, Arnold-Chiari type I malformation and basilar impressio
n. Preoperative polysomnography showed dysrhythmic breathing and brady
pnea during sleep. Abnormal breathing improved after suboccipital deco
mpression craniotomy and upper cervical laminectomy. It was suggested
that dysrhythmic breathing was caused by a disorder of the medullary r
espiratory center. Herniation of the cerebellar tonsil and syringomyel
ia might have compressed the medulla.