Artery Of Percheron Occlusion Research Articles

Successful Thrombolysis in Artery of Percheron Infarction: Grabbed an Extremely Rare Opportunity

Artery of Percheron (AOP) is an uncommon anatomical variation in the posterior circulation neurovasculature. It is a single artery arising from P1 segment of posterior cerebral artery (PCA) which supplies bilateral paramedian thalami and the rostral midbrain and as a result, occlusion of it leads to bilateral thalamic and mesencephalic infarction. Due to very low incidence (ranges from 0.1% to 2% of all ischemic strokes) and varied presentation, the diagnosis of AOP infarction requires strong clinical and radiological suspicion and hence, AOP infarction is often missed and patients are rarely thrombolysed. Here we discuss a patient with acute altered sensorium who recovered completely in short time following treatment with intra-venous thrombolysis for bilateral medial thalamic ischemic stroke due to AOP occlusion.

Transient Movement Disorder Following Artery of Percheron Occlusion (P9-5.024)

Transient Movement Disorder Following Artery of Percheron Occlusion (P9-5.024)

Bilateral Thalamic Infarction Related to Artery of Percheron with Microembolic Signal

The artery of Percheron (AOP) is an uncommon variant of the posterior cerebral artery that supplies blood to the paramedian thalamus and rostral midbrain. AOP is often difficult to recognize with intracranial magnetic resonance angiography due to its small size. Although a number of case reports of AOP occlusion have been published, cause of the occlusion is mostly unclear. We experienced a case of AOP occlusion which resulted in bilateral thalamic infarction. It was most likely caused by a microembolism through right-left shunt.

Magnetic resonance angiography validation of bilateral thalamic infarction induced by artery of Percheron occlusion: a case description

Magnetic resonance angiography validation of bilateral thalamic infarction induced by artery of Percheron occlusion: a case description

Successful Outcome in an Adolescent with Artery of Percheron Occlusion who was Treated with Tissue Plasminogen Activator

BackgroundIschemic stroke is relatively rare in children, leading to a low level of suspicion and delayed diagnosis, particularly in cases of posterior circulation occlusion when symptoms are less indicative. Occlusion of the artery of Percheron (AOP) results in nonspecific neurologic symptoms, including drowsiness, aphasia or dysarthria, ophthalmoplegia, ataxia, and dysmetria. Previous reports, mainly in adults, described late diagnosis and severe residual disability. Case ReportWe report a case of a 16-year-old male who presented to the pediatric emergency department with altered mental status. There was no history of trauma or intoxication. The main symptoms included confusion, slurred speech, and multiple falls starting 1 h before arrival to the emergency department. No motor deficits or other focal signs were noticed. The patient's consciousness gradually decreased followed by apneic events. Routine laboratory tests, urinary toxic screen, and a computed tomography scan of the head were normal. A magnetic resonance imaging scan of the brain revealed bilateral restrictive changes in the thalamus. A diagnosis of AOP occlusion was made, and the patient was treated with tissue plasminogen activator (6 h after symptom onset). He was extubated on day 4 and discharged on the day 10 of admission without any neuropsychological deficit. Why Should an Emergency Physician Be Aware of This?Posterior circulation stroke in the pediatric population is a diagnostic challenge that often results in suboptimal treatment and unfavorable outcomes. Prompt imaging studies in children with nonspecific altered mental status enable timely diagnosis and thrombolytic treatment that may substantially improve the outcome.

Stroke due to Percheron Artery Occlusion: Description of a Consecutive Case Series from Southern Portugal.

The artery of Percheron (AOP) is an abnormal variant of the arterial supply of the thalamus. Stroke caused by AOP occlusion is seldom reported. AOP leads to bilateral thalamic and rostral midbrain infarct presenting with unspecific manifestations. There are few descriptions of case series of stroke caused by AOP. We sought to review the clinicoradiological characteristics of AOP infarction from Algarve, Southern Portugal. Eight consecutive cases were retrospectively identified by searching the electronic clinical charts, as well as the stroke Unit database (2015–2020). Sociodemographic (age and gender) and clinicoradiological characteristics (etiological classification, admission severity, manifestations, and short- and long-term prognoses) were retrieved. The corresponding frequency of AOP infarction was 0.17% (95% confidence interval: 0.05–0.28). The mean age was 67.1 (range: 60–80) years. The range of stroke severity evaluated assessed by the National Institute of Health Stroke Scale ranged from 5 to 23 (median = 7.5). None of the patients receive acute ischemic stroke reperfusion treatment. AOP patterns were isolated bilateral paramedian thalamic ( n = 2), bilateral paramedian and anterior thalamic ( n = 2), and bilateral paramedian thalamic with rostral midbrain ( n = 4). Two patients (20%) died on the short term (30 days). At hospital discharge, six patients had functional disability of ≤2 on the modified Rankin scale. In the follow-up at 6 months, half ( n = 3) of the survivors had persistent hypersomnia and two had vascular dementia. Stroke from AOP presents with variable clinical and radiological presentations and patients do not receive alteplase. The short-term survivor and the long-term functional independency can be compromised after AOS infarct.

Artery of Percheron Ischaemic Stroke: A Classic Presentation of a Rare Case.

The artery of Percheron (AoP) is a rare anatomic variant, where the paramedian thalami and the rostral midbrain are supplied by an artery emerging from the P1 segment of the posterior cerebral artery. Ischaemic infarction of the artery of Percheron occurs rarely, accounting for 0.1 to 2% of all ischaemic strokes. AoP occlusion can lead to an infarction of the paramedian thalami and mesencephalon, resulting in a triad of clinical features; namely, altered mental status, vertical gaze palsy and memory impairment. A larger mesencephalon infarction can also feature oculomotor disturbances. We describe here the case of an 88-year-old patient, presenting with this triad of features.LEARNING POINTSNeurological events such as ischaemic strokes can have a wide clinical presentation.Artery of Percheron infarction is characterized by memory impairment, vertical gaze palsy and altered mental status.Pattern recognition is fundamental for early diagnosis and optimal care.

Artery of Percheron Occlusion: A Diagnostic Challenge.

Artery of Percheron occlusion is a rare cause of ischaemic stroke characterized by bilateral thalamus infarction. Presentation is varied and non-specific, with the most frequent manifestations being altered level of consciousness, hypersomnolence or altered oculomotor movements. We describe the case of a 37-year-old man hospitalized for hypersomnia and hypomnesia with 3 days of evolution, who was diagnosed with a bilateral thalamus stroke due to artery of Percheron occlusion.LEARNING POINTSStroke is frequently encountered but can present a diagnostic challenge when presentation is non-specific or a lesion is not identified.Artery of Percheron stenosis has a varied and often non-specific presentation, which can lead to delayed diagnosis and treatment of these patients.It is important that doctors recognize this entity for timely diagnosis and treatment, and for the best prognosis.

Intravenous thrombolytic therapy for cerebral infarction due to the Persheron artery occlusion. Case report

Occlusion of the artery of Percheron is the cause of bilateral thalamic infarctions, sometimes involving structures of the midbrain. A clinical case of intravenous thrombolytic therapy for ischemic stroke due to the occlusion of the Percheron artery in a 72-year-old female patient who developed depression of consciousness, oculomotor disorders, dysarthria, ataxia, pyramidal disorders, and cognitive disorders is presented. Magnetic resonance imaging, which detected bilateral thalamus paramedian infarction in the acute stage, made it possible to diagnose the occlusion of the Percheron artery. Intravenous thrombolysis led to a rapid regression of symptoms; at the end of the acute period of the disease, the patient was discharged from the hospital with a slight neurological deficit and with a good functional outcome. After a one year the dynamic observation revealed persistent mild cognitive disorders; magnetic resonance imaging showed small symmetric cystic-gliosis changes in the medial parts of the thalamus on both sides. Timely diagnosis and intravenous thrombolytic therapy contribute to a good outcome of cerebral infarction due to the Percheron's artery occlusion.

Topographic evaluation of bithalamic infarcts: Are these due to occlusion of the artery of Percheron?

Occlusion of the artery of Percheron (AoP) causes bithalamic paramedian infarct (BTPI). Although it can be diagnosed easily in its pure form, it can be underdiagnosed in cases with concomitant extrathalamic acute infarcts (plus-BTPI) as it may be difficult to determine whether BTPI is due to occlusion of AoP or two different paramedian arteries even with conventional angiography. This study was performed to highlight plus-BTPI that could result from occlusion of AoP rather than of two distinct paramedian arteries using topographic evaluation of bithalamic infarcts. We retrospectively reviewed imaging and clinical databases for patients admitted to radiology department between 2013 and 2019. Two radiologists independently evaluated the results of imaging studies, and findings reached by consensus were used in the analysis. This retrospective review yielded 34 patients with bithalamic infarct. Each affected thalamic vascular region was investigated separately. Any patient could have more than 2 different vascular zone infarct. The affected thalamic vascular territories were paramedian (n = 24), inferolateral (n = 13), anterior (n = 10), and posterior (n = 7). When we evaluated bithalamic infarcts in terms of symmetrically affected territories, the distribution of symmetric affected territories was as: paramedian (n = 18), inferolateral (n = 2), anterior (n = 1), and posterior (n = 1). BTPI had a 4.5-fold higher frequency than the sum of symmetric involvement of other territories (p = 0.0552, OR = 4.5,95%CI 0.93–21.5). In addition, mesencephalic involvement was only observed in BTPI, and not in other patterns (p < 0.001).The fact that in bilateral thalamic infarcts the symmetric involvement of paramedic territory is significantly higher and mesencephalic involvement is seen only in BTPI can suggest that plus-BPTI may develop due to AoP occlusion rather than occlusion of two distinct paramedian arteries.

Percheron’s Occlusion: Difficulty of Clinical Diagnosis about One Case in the Teaching Hospital of Cocody (Abidjan-RCI)

Ischemic strokes have varying etiologies and multiple locations. Some locations are much rarer than others and just as difficult to diagnose. This is the case of the ischemic bi-thalamic stroke, attributable to the Percheron artery occlusion that we report in a 33-year-old woman with a history of taking estrogen-progestin. The lesion diagnosis could only be possible thanks to the performance of brain MRI, thus testifying to the diagnostic difficulties observed. Etiological research has shown dyslipidemia. The length of stay was 88 days. At the end of intensive care, the patient was conscious, not deficient and did not present memory disorders.

Bilateral thalamic infarction secondary to artery of Percheron occlusion: A rare cause of acute coma

An occlusion of the artery of Percheron (AOP) is a rare clinical condition that remains a diagnostic challenge for physicians given its variable presentation. This infarction is a result of an anatomical variant of a single vessel arising from the posterior cerebral artery. Occlusion of the AOP results in variable levels of alteration of consciousness, vertical gaze palsy, and memory impairment. Unfortunately, due to this variable presentation these strokes are often missed. We report a case of a 71 year-old-female who presented with sudden onset of unresponsiveness who was subsequently diagnosed with bilateral thalamic infarction with midbrain involvement secondary to AOP occlusion. Delayed diagnosis can result in poor neurologic outcomes as demonstrated in this case making it imperative to bring further awareness to this clinical syndrome.

Acute bilateral thalamic infarctions with midbrain involvement due to artery of Percheron occlusion

The artery of Percheron is a single dominant vessel of posterior cerebral artery which supplies the thalamus bilaterally. It is a rare variant of arterial supply to the paramedian thalami. The classical triad of presentation of artery of Percheron occlusion is vertical gaze palsy, memory impairment, and alteration of mental status. Here we report a case of artery of Percheron occlusion where the patient presents with classic features of thalamic infarction associated with the midbrain involvement evidenced by the presence of bilateral hemiparesis. When compared to the typical thalamic infarction alone, the prognosis is worse when midbrain is also affected.

Secondary Bithalamic Ischemic Vascular Accident Has an Occlusion of the Artery of Percheron

The bithalamic ischemic stroke secondary to percheron artery occlusion occupies a small place in the large ischemic stroke family, but its clinical polymorphism arouses patrician curiosity. We thus report 3 observations that explain the richness of this affection.

Bilateral thalamic stroke in patient with patent foramen ovale and hereditary thrombophilia

Patent foramen ovale and hereditary thrombophilia are both known risk factors for ischemic stroke. Artery of Percheron is a rare anatomical variant in which vast areas of the midbrain and thalamus have a single source of blood supply. This case report presents a 45-years old female patient with bilateral thalamic stroke due to Percheron artery occlusion, with a combination of hereditary thrombophilia and patent foramen ovale as the risk factors. Modern approaches to the diagnosis and secondary prevention of this pathology are also discussed herein.

Persistent anterograde amnesia due to the artery of Percheron occlusion: a case report

ABSTRACTBilateral thalamic infarction involving the artery of Percheron (AOP) can cause diagnostic difficulties due to the varying clinical presentations. AOP infarcts presented with isolated memory impairment are not common and the factors affecting the persistence of memory disorders are still unknown. A 41-year-old male patient was hospitalized with acute unconsciousness. MRI disclosed bilateral paramedian thalamic infarction The patient had isolated memory deficit and his anterograde amnesia continued without any change in the past decade. More cases might answer the questions concerning the intra- and extra-thalamic structures responsible for the amnesic syndrome and the factors affecting the persistence of the symptoms.

Artery of percheron occlusion: a rare cause of coma

Objectives To present a case of artery of Percheron (AOP) occlusion and discuss the neuroimaging and clinical differential diagnosis. Case A 40-year-old male with no past medical history was found unconscious by his work colleagues. On presentation, he had a GCS of 7 (E3, V1, M3) and a left dilated unreactive pupil. He had no witnessed seizure activity and displayed no focal neurological deficits. Immediate brain imaging showed no evidence of intracranial haemorrhage or basilar artery occlusion. He was intubated and treated empirically for seizures and encephalitis. Lumbar puncture was negative and an EEG performed 24 hours later revealed no seizure activity. An MRI done 72 hours after the event revealed bi-thalamic infarction, suggestive of AOP occlusion. He was extubated 4 days after presentation. He displayed intermittent drowsiness throughout the day, as well as a vertical gaze palsy. Mobility was significantly impaired secondary to reduced dynamic balance but he had no sensory or motor deficits and no cerebellar signs. MRI scans revealed an associated small left cerebellar hemisphere infarct, suggesting an embolic aetiology. The patient underwent a full young stroke work-up, including vasculitic and thrombophilia screen, which were unremarkable. Transoesophageal echocardiography identified no cardiac source of embolus and no patent foramen ovale. The decision was made to commence anti-coagulation with apixaban. Three-weeks post onset, the patient had an ongoing vertical gaze palsy but improved levels of alertness, and is awaiting in-patient rehabilitation to improve mobility. Conclusions AOP occlusion is a rare cause of coma and should be suspected in patients who present with acute loss of consciousness, once other common aetiologies are excluded. This case raises pertinent questions regarding the indications and benefits of thrombolysis and/or clot retrieval in such patients.

Acute Occlusion of the Percheron Artery during Pregnancy: A Case Report and a Review of the Literature

The Percheron artery (PA) is a rare variant vessel. Its acute occlusion can cause a bilateral symmetrical thalamic stroke, clinically manifested as a sudden alteration of consciousness that could vary from sleepiness to coma. In this paper, we illustrate a case of acute PA occlusion in a young, pregnant woman and present a review of the literature, focusing on the possible causes of the acute occlusion. A 35-year-old woman, at the fourth week of pregnancy, came to the emergency department of our hospital because of a sudden onset and persistent loss of consciousness. Brain magnetic resonance imaging (MRI) showed a symmetrical and bilateral thalamic infarction without evidence of other ischemic lesions, compatible with an acute PA occlusion. The patient, who showed full clinical recovery within a few hours of symptom onset, received a short-term anticoagulant treatment followed by aspirin for long-term prevention. We reviewed the literature about the possible causes of acute PA occlusion. This ischemic condition is usually associated with cardioembolic or small-vessel disease. However, in our patient, we did not find any element supportive for coagulative alteration or embolyzing conditions. The presence of this type of thalamic stroke should be considered in the management of persistent loss of consciousness. PA occlusion is rare, but it needs a brain MRI examination for a correct diagnosis, a narrow evaluation of all the possible causes, and a long-term anticoagulant therapy. Pregnancy itself should constitute a rare but possible cause of a PA occlusion.

Bilateral thalamic infarction due to artery of percheron occlusion with corresponding CT perfusion abnormalities

Background: The Artery of Percheron (AOP) is a rare anatomic variant that supplies the bilateral medial thalami from a common origin; occlusion results in a characteristic pattern of bilateral thalamic infarction seen on neuroimaging. To date, we have not identified any cases in the literature describing corresponding ischemic changes seen on hyperacute CT Perfusion imaging. We aimed to characterize perfusion abnormalities seen in AOP occlusion by describing a case presentation, highlighting the importance of recognizing this syndrome clinically, and radiologically, in an acute stroke presentation. Methods: Description of a case, and literature search on PubMed. Results: A 74-year-old man was seen in the ER as a Code Stroke protocol with acute alteration of level of consciousness (LOC). ER assessment showed no focal abnormalities and was significant only for disorientation. CT/CTA/CTP initially appeared unremarkable for acute abnormalities. His LOC deteriorated requiring intubation, and subsequent MRI showed bilateral thalamic infarction. Further CT Perfusion review demonstrated increased Mean Transit Time and decreased Blood Flow without Volume abnormalities in the bilateral paramedian thalami. Conclusion: AOP infarction is an uncommon cause of bilateral thalamic infarction. We have demonstrated a case highlighting perfusion abnormalities not previously reported in AOP occlusion, illustrating the importance and utility of advanced CT perfusion imaging whilst considering less common stroke syndromes.

Bilateral thalamic ischemic stroke caused by Percheron artery occlusion with onset of disturbance of consciousness: one case report

Bilateral thalamic ischemic stroke caused by Percheron artery occlusion with onset of disturbance of consciousness: one case report