Abstract：
:The Gasperini syndrome is a very rare brainstem disease characterized by the typical combination of ipsilateral lesions of the cranial nerves V-VII and dissociated contralateral hemihypesthesia, whereas both contralateral and ipsilateral hypacusis was described. Since the first description in 1912, only a few cases of this crossed brainstem syndrome were published so far. Pontine infarction and bleedings were the reported causes of the syndrome. Here we report a 44-year-old man with the classical Gasperini syndrome due to pontine demyelination in multiple sclerosis. The clinical findings were correlated with changes on MRI. The present case shows that classical crossed brainstem syndromes are topological terms not invariably associated with brainstem ischemia in particular vascular areas and may contribute to the differential diagnosis of peripheral facial nerve palsy.
journal_name
Eur J Med Resjournal_title
European journal of medical researchauthors
Krasnianski M,Müller T,Zierz S,Winterholler Mdoi
10.1186/2047-783x-14-9-413subject
Has Abstractpub_date
2009-09-01 00:00:00pages
413-4issue
9eissn
0949-2321issn
2047-783Xjournal_volume
14pub_type
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journal_title：European journal of medical research
pub_type： 临床试验,杂志文章
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abstract：BACKGROUND:In subtotal central retinal artery occlusion (CRAO), distinct retinal edema with acute onset irreversible visual loss is common. - METHODS:Clinical observation, fluorescein angiogram. - PATIENT:A 69-year-old patient presented with acute visual loss of his right eye. Risk factors for CRAO were arterial hype...
journal_title：European journal of medical research
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pub_type： 杂志文章,多中心研究
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journal_title：European journal of medical research
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journal_title：European journal of medical research
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pub_type： 杂志文章,meta分析
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