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.

Thalamo-mesencephalic Branches of the Posterior Cerebral Artery: a 3D Rotational Angiography Study.

PURPOSE: The thalamo-mesencephalic (TM) branches of the posterior cerebral artery (PCA) supply critical structures. Previous descriptions of these vessels are inconsistent and almost exclusively rely on cadaver studies. We aimed to provide a neuroradiological description of TM vessels in vivo based on routine 3D rotational angiographies (3D-RA). METHODS: We analyzed 3D-RAs of 58 patients with pathologies remote from the PCA. PCA-origins were considered. Delineation, origin and number of branches of the collicular artery (CA), the accessory CA (ACA), the posterior thalamoperforating artery (PTA), the thalamogeniculate artery (TGA), and the posterior medial (PMCA) and lateral (PCLA) choroid arteries were assessed. The PTAs were categorized based on Percheron's suggested classification. RESULTS: A CA was identified in 84%, an ACA in 20%. The PTA was delineated in 100%. In 27%, PTA anatomy had features of several Percheron types (n = 7) or vessels emanating from a net like origin (n = 9). 26% had a type IIb PTA. A fetal type PCA origin with hypoplastic ipsilateral P1 was observed in 5 cases with type IIa (n = 2) or type IIb (n = 3) PTAs originating from contralateral P1. The TGA was identified in 85% of patients, with ≥ 2 branches in 67%. The PMCA was delineable in 41%, the PLCA in 100%. CONCLUSION: The prevalence of a proper "Artery of Percheron" type IIb PTA seems to be higher than previously reported. A fetal type P1-origin may be predictive of a type IIa/b PTA emanating from contralateral P1. 3D-RA may be useful for planning PCA interventions, as impairment of TM branches is a severe risk.

Infarto da artéria de Percheron: relato de caso / Percheron´s artery infarction: a case report

O infarto da artéria de Percheron é uma apresentação rara de acidente vascular cerebral, caracterizado principalmente por isquemia talâmica bilateral. A apresentação clinica desse infarto se apresenta de maneira inesperada e variável. Relata-se um caso de um paciente masculino, idoso, acometido por diversas comorbidades, admitido na emergência em coma e hemiplégico a direita, demonstrando acometimento neurológico. A condição clínica do paciente variou durante a hospitalização, apresentando melhora do quadro neurológico focal e midríase fixa à direita, levando a um diagnóstico tardio. Paciente evoluiu ao óbito devido a causas não neurológicas.

The artery of Percheron infarct is a rare presentation of stroke, featured mainly by thalamic bilateral ischemia. The clinical presentation of this infarct is unexpected and variable. It's reported a case of a male patient, elderly, affected with several comorbidities, admitted to the emergency in comatose state and right hemiplegic, proving neurological involvement. The patient's clinical condition has fluctuated throughout the hospitalization presenting improvement of the focal neurologic implication and right mydriasis, culminating in a lagged diagnosis. Patient's death due to non neurologic causes.

Síndrome de Percheron / Percheron syndrome

El infarto talámicoparamediano bilateral sincrónico,llamado habitualmente infarto de la arteria de Percheron, se considera infrecuente y de difícil diagnóstico clínico. Se presenta a una paciente de 50 años, con infarto talámico bilateral, que presentó un cuadro de desorientación, visión borrosa y doble en horas de la mañana, sin referir pérdida de conciencia. En la tomografía axial computarizada de cráneo simple se evidenció una hipodensidad talámica bilateral, compatible con un infarto agudo a este nivel, por oclusión de la arteria de Percheron. Es importante el reconocimiento de esta variante anatómica para establecer el mecanismo del infarto talámico bilateral.

Síndrome de Percheron / Percheron syndrome

El infarto talámicoparamediano bilateral sincrónico, llamado habitualmente infarto de la arteriade Percheron, se considera infrecuente y de difícil diagnóstico clínico. Se presenta a una paciente de 50 años, con infarto talámico bilateral, que presentó un cuadro de desorientación, visión borrosa y doble en horas de la mañana, sin referir pérdida de conciencia. En la tomografía axialcomputarizada de cráneo simple se evidenció una hipodensidad talámica bilateral, compatible con un infarto agudo a este nivel, por oclusión de la arteria de Percheron. Es importante elreconocimiento de esta variante anatómica para establecer el mecanismo del infarto talámicobilateral(AU)

Infarto agudo talámico bilateral en paciente joven con foramen oval permeable / Acute bilateral thalamic infarcts in a young man with patent foramen ovale

Antecedentes: La presencia de foramen oval permeable se asocia a infartos cerebrales criptogénicos en pacientes jóvenes. Caso clínico: Hombre de 27 años en quien se inició de forma súbita síndrome confusional agudo, bradipsiquia y somnolencia. La imagen de resonancia magnética cerebral mostró infarto talámico bilateral simétrico por probable oclusión de arteria de Percheron tipo 2b. El ecocardiograma identificó foramen oval permeable. Conclusiones: El evento cerebrovascular es causa frecuente de discapacidad e incluso muerte en población joven. Debe hacerse énfasis en el estudio integral de esta patología.

BACKGROUND: Patent foramen ovale (PFO) has been associated with cryptogenic stroke in young patients. CLINICAL CASE: A 27-year-old man presented with acute confusional syndrome, altered language, bradypsychia and somnolence. Brain MRI showed symmetrical bilateral thalamic infarctions probably due to occlusion of Percheron's artery type 2b. Echocardiography showed patent foramen ovale. CONCLUSIONS: Cerebrovascular disease is a frequent cause of disability and even death in young patients, and thus its medical approach should be emphasized.

Bipolar disorder complicated by selfmutilation: neurofunctional changes demonstrated by Tc99mHMPAO Neuro SPECT

We report neurofunctional changes in patients with selfmutilation and bipolar disorder. We compared a sample of 29 patients with selfmutilation and bipolar disorder with a group of 20 patients with bipolar disorder without selfmutilation. Furthermore we had an additional control of 22 patients with Major Depression without selfmutilation. Among the findings in selfmutilation, increased anterior dorsal-ventral thalamic perfusion stands out, this is associated with decreased perfusion in the perilimbic area (areas 24, 32 and 23 of Brodmann). There are multiple reports relating in animals and humans selfmutilation with hypoalgesia, anesthesia and disestesias; an hypothesis can be formulated relating self mutilation phenomena with a dysfunction of thalamus and perilimbic circuits associated with nosoceptive circuits and somato-psychic conscience.

Hypersexuality following bilateral thalamic infarction: case report

Hiperssexualidade é uma condição rara mas bem reconhecida após lesão do sistema nervoso central. A literatura medica registra casos secundários a disfunção do hipotálamo, do lobo temporal e do lobo frontal. Relatamos o caso de um homem de 63 anos de idade que desenvolveu alterações neuropsicológicas com hiperssexualidade como característica mais proeminente, desinibição, moderada perda de memória, hipersonia e irritabilidade após infarto talâmico paramediano bilateral. O SPECT evidenciou hipoperfusão frontal. Nós acreditamos que esses achados sejam expressão da disfunção de circuitos córtico-subcorticais frontais, particularmente do circuito órbito-frontal, secundária ao infarto dorsomedial do tálamo, que provavelmente desempenha papel relevante na determinação do comportamento sexual humano. Este caso favorece uma possível função moduladora do tálamo sobre os circuitos córtico-subcorticais frontais.

Bilateral Paramedian Thalamic Contrast Enhancement on CT after Intra-arterial Thrombolysis

A 58-year-old woman presented with an acute embolic occlusion of the distal basilar artery. She underwent angioplasty and intra-arterial thrombolysis. Angiography performed after recanalization revealed a single perforating thalamic artery. A nonenhanced CT scan carried out immediately after the procedure revealed hyperdense lesions in the bilateral paramedian portions of the thalami, which disappeared on the 24-hour follow-up CT scan. Three months later, the patient improved to functional independence, but had some memory dysfunction and vertical gaze palsy. This case suggests that contrast enhancement or extravasation can occur in the thalamus after intra-arterial thrombolysis performed to recanalize a basilar artery occlusion.

Infartos talámicos bilaterales y simultáneos / Bilateral, simultaneous thalamic infarctions

Se presentan tres casos de infartos talámicos bilaterales y simultáneos, haciéndose una revisión histórica de la patología isquémica talámica a partir de la descripción inicial del síndrome talámico de Dejerine y Roussy. Se describe la vascularización talámica y la clínica del infarto talámico, correlacionándola con los hallazgos tomográficos y discutiéndose los mecanismos etiopatogénicos

Distonia virtual por infarto talâmico posterolateral ventral: relato de caso / Virtual dystonia due to a posteroventrolateral thalamic infarct: case report

O presente trabalho relata o caso de um diabético hipertenso acometido de uma forma fragmentária da síndrome de Dejerine-Roussy e "sensaçao de câimbra dolorosa" nos artelhos quando se deitava ou removia o pé do contato com o chao. A propriocepçao estava acentuadamente comprometida nos artelhos que abrigavam a câimbra. Seu relato se adequava ao padrao das distonias fixas, nao transcrita, todavia, como deformidade motora visível razao pela qual designamos o fenômeno de "distonia virtual". A RNM mopstrou imagem infarto do núcleo lateral posterior do tálamo (VPL) e degeneraçao walleriana de projeçoes VLP-corticais. O SPECT, exclusao do tálamo e hipoperfusao do córtex parietal dorsal ipsilateral e dos núcleos da base bilateralmente. Sugerimos que, em decorrência da interrupçao de aferentes proprioceptivos no tálamo, o córtex somestésico (S-I) originou atividade topograficamente ordenada que emergiu sob a forma de distonia como representaçao mental subjetiva. Sugerimos que a distonia virtual represente o análogo somestésico das alucinoses unimodais, cujo exemplo mais conhecido é a síndrome de Bonnet.

Fabry's disease in a female carrier with bilateral thalamic infarcts: a case report ans a family study

Relata-se o caso de uma jovem, heterozigota para doença de Fabry, que desenvolveu infartos talâmicos bilaterais por oclusäo de vasos do sistema nervoso central. Três outros membros de sua família foram também avaliados. A doença de Fabry inclui-se entre as causas raras de acidente vascular cerebral em adultos jovens