Lateral pontine syndrome
Lateral pontine syndrome | |||||||||||||||||
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cranial nerve nuclei of the pons.[2]
HistoryLateral pontine syndrome was first described in France by French neurologists Pierre Marie (1853-1940), Charles Foix (1882-1927), and Théophile Alajouanine (1890-1980) in 1922. They were the first to identify and describe the symptoms and causes of this syndrome. In their original description, they reported findings from autopsies that showed spinal cord necrosis and multiple tortuous and thickened blood vessels on the surface of the spinal cord. This condition was later called necrotizing myelopathy.[3] They emphasized that in their two cases, no thrombosis was present. They considered the vascular component of the entity they reported to be a wall thickening, without luminal narrowing or obliteration of the cord vessels (arteries as well as veins). They addressed, and ruled out, the possibility of vascular malformations.[4] SymptomsDamage to the following areas produces symptoms (from medial to lateral):
CausesThe syndrome occurs due to occlusion of perforating branches of the basilar and anterior inferior cerebellar (AICA) arteries.[5][6][7] It can also be caused by an interruption to the blood supply of the anterior inferior cerebellar artery or circumferential arteries.[8] TreatmentThe treatment for lateral pontine syndrome varies greatly, so there are different medications for different symptoms.[9] Sometimes blood thinning agents are prescribed to remove blood flow hindrance.[10] Other than these medications, physical therapy is also necessary[11] References
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