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Artery of Percheron (AOP) is a rare anatomical variant, which supplies bilateral paramedian thalami and the rostral mesencephalon via a single dominant thalamic perforating artery arising from the P1 segment of a posterior cerebral artery. AOP infarcts can present with a plethora of neurological symptoms: altered mental status, memory impairment, hypersomnolence, coma, aphasia, and vertical gaze palsy. Given the lack of classic stroke signs, majority of AOP infarcts are not diagnosed in the emergency setting. Timely diagnosis of an acute bilateral thalamic infarct can be challenging, and this case report highlights the uncommon neurological presentation of AOP infarction. The therapeutic time window to administer IV tPA can be missed due to this delay in diagnosis, resulting in poor clinical outcomes. To initiate appropriate acute ischemic stroke management, we propose a comprehensive radiological evaluation in the emergency room for patients with a high suspicion of an AOP infarction.
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http://dx.doi.org/10.1155/2019/1260865 | DOI Listing |
Neuroradiol J
August 2025
Department of Medical Surgical Sciences and Advanced Technologies "GF Ingrassia", University Hospital Policlinico "G. Rodolico-San Marco", Radiology Unit 1, Italy.
Artery of Percheron (AOP) infarction is a rare form of ischemic stroke resulting from the occlusion of a single arterial trunk that supplies both sides of the paramedian thalamus and the midbrain. Its occlusion can lead to bilateral and symmetrical infarctions of the paramedian thalami, and occasionally, the midbrain. Due to its atypical presentation, this condition is often diagnosed late.
View Article and Find Full Text PDFAnn Med Surg (Lond)
July 2025
Department of Neurosurgery, College of medical sciences,Bharatpur 44200, Nepal.
The artery of Percheron (AOP) infarction is a rare vascular condition and a pattern of ischemia where a single arterial trunk supplies blood to the rostral midbrain and paramedian thalamic areas, causing neurological deficits. Due to its rarity and atypical presentation, AOP infarction is frequently overlooked in initial assessments, particularly on computed tomography (CT) scans. In addition, different types of AOP infarction have been identified, and it is shown that there can be four significant distinct types of this disease, which may manifest some different symptoms and have various vascular alterations.
View Article and Find Full Text PDFCureus
July 2025
Internal Medicine, Mid City Hospital Multan, Multan, PAK.
Bilateral thalamic infarcts represent an uncommon manifestation of acute ischemic stroke, often resulting from occlusion of the artery of Percheron (AOP). Thereby, we report the case of an 86-year-old female with a background of multiple comorbidities who presented with sudden-onset unresponsiveness. Her Glasgow coma scale (GCS) score on admission was 10/15.
View Article and Find Full Text PDFFront Surg
July 2025
Department of Neurosurgery, Huashan Hospital, Shanghai Medical College, Fudan University, Shanghai, China.
Background: Occlusion of the artery of Percheron (AOP), a rare variant of the paramedian thalamic artery, leads to bilateral paramedian thalamic infarction with or without midbrain involvement. AOP following surgical clipping of anterior circulation aneurysms has not been documented in the literature.
Case Description: A 59-year-old female patient presented with recurrent dizziness and diplopia, for which she subsequently received dual antiplatelet therapy.
Am J Case Rep
July 2025
Department of Medicine, College of Human Medicine, Michigan State University, East Lansing, MI, USA.
BACKGROUND Wernicke's encephalopathy (WE) and Artery of Percheron (AOP) infarction share overlapping presentations, including mental status changes, ocular-motor signs, and similar thalamic MRI findings; but require distinct time-sensitive treatment, making prompt differentiation critical. WE results from thiamine deficiency, often due to alcohol use, causing oxidative damage in highly metabolically active brain regions. In contrast, an AOP infarction results from thrombotic occlusion of a rare perforating artery.
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