Khalid Jumean, Ahmad Abu Arqoub, Moayad Awni Al Hadidi, Amer Hawatmeh, Hamid Shaaban
Department of Internal Medicine, Hematology and Oncology, St. Michael’s Medical Center, Newark, New Jersey, USA.
DOI: 10.4103/0976-9668.175108


The artery of Percheron (AOP) is a rare vascular variant in which a single dominant thalamoperforating artery arises from the P1 segment and bifurcates to supply both paramedian thalami. Occlusion of this uncommon vessel results in a characteristic pattern of bilateral paramedian thalamic infarcts with or without mesencephalic infarctions. We report a case of a 37-year-old man with acute bilateral thalamic infarcts. The scans revealed symmetric bilateral hyperintense paramedian thalamic lesions consistent with an acute ischemic event. The posterior circulation was patent including the tip of the basilar artery and both posterior cerebral arteries, making the case compatible with occlusion of the AOP. This type of infarct is associated with embolic phenomena, and further evaluation revealed a patent foramen ovale as the source of emboli in the cerebrovascular circulation. The occlusion of the AOP is a rare cause of coma in young patients, and early recognition of this rare disease entity may lead to more favorable outcomes.

Keywords: Artery of Percheron, bilateral thalamic infarcts, patent foramen ovale.

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