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Spontaneous Vertebral Artery Dissection and Thrombosis Presenting as Lateral Medullary Syndrome

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DOI https://doi.org/ 10.1055/s-0039-1697243 ISSN 0976-3147. ©2019 Association for Helping Neurosurgical Sick People A 28-year-old male patient had acute-onset headache, vomiting, vertiginous sensation, and diplopia of 3 days’ duration. Patient, in… Click to show full abstract

DOI https://doi.org/ 10.1055/s-0039-1697243 ISSN 0976-3147. ©2019 Association for Helping Neurosurgical Sick People A 28-year-old male patient had acute-onset headache, vomiting, vertiginous sensation, and diplopia of 3 days’ duration. Patient, in the past, had recurrent episodes of migraine. General examination was normal. Cranial nerve examination showed left torsional nystagmus, left Horner’s syndrome, decreased pain, and temperature sensation over the left side of the face and decreased pain and temperature sensation over the right side of the body. Power in limbs was normal. Magnetic resonance imaging and computed tomography angiography showed partially thrombosed left vertebral artery aneurysm proximal to the basilar confluence with mass effect and acute infarct on lateral medulla. The patient had left lateral medullary syndrome (►Fig. 1). Patient was treated conservatively. The presumed pathogenetic mechanisms for lateral medullary syndrome are large vessel infarction (50%), arterial dissection (15%), small vessel infarction (13%), and cardiac embolism (5%). In a young patient with migrane, presenting with lateral medullary syndrome, vertebral artery dissection and aneurysm should be suspected.1,2 J Neurosci Rural Pract 2019;10:502–503

Keywords: patient; medullary syndrome; vertebral artery; lateral medullary

Journal Title: Journal of Neurosciences in Rural Practice
Year Published: 2019

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