Raymond Céstan syndrome
Raymond Céstan syndrome, also known as Céstan–Chenais syndrome or upper dorsal pontine syndrome, is caused by blockage of the long circumferential branches of the basilar artery.[1] It was described by Étienne Jacques Marie Raymond Céstan and Louis Jean Chenais.[2] Along with other related syndromes such as Millard-Gubler syndrome, Foville's syndrome, and Weber's syndrome, the description was instrumental in establishing important principles in brain-stem localization.[3]
Clinical features
- Ipsilateral ataxia and coarse intention tremor (damage to superior and middle cerebellar peduncle)
- Ipsilateral paralysis of muscles of mastication and sensory loss in face (damage to sensory and motor nuclei and tracts of CN V)
- Contralateral loss of sensory modalities in the body (damage to spinothalamic tract and medial lemniscus)
- Contralateral hemiparesis of face and body (damage to corticospinal tract) may occur with ventral extension of lesion
- Horizontal gaze palsy may occur (as in lower dorsal pontine syndrome)
References
- ↑ http://www.clineu-journal.com/article/S0303-8467(07)00181-3/abstract
- ↑ http://www.whonamedit.com/synd.cfm/618.html
- ↑ Silverman, IE; Liu, GT; Volpe, NJ; Galetta, SL (June 1995). "The crossed paralyses. The original brain-stem syndromes of Millard-Gubler, Foville, Weber, and Raymond-Cestan". Archives of neurology.
- Further reading
- Kim, JS; Lee, JH; Im, JH; Lee, MC (Jun 1995). "Syndromes of pontine base infarction. A clinical-radiological correlation study.". Stroke; a journal of cerebral circulation 26 (6): 950–5. doi:10.1161/01.STR.26.6.950. PMID 7762044.
- Krasnianski, M; Neudecker, S; Zierz, S (Aug 2004). "[Classical crossed pontine syndromes].". Fortschritte der Neurologie · Psychiatrie (in German) 72 (8): 460–8. doi:10.1055/s-2004-818392. PMID 15305240.
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