AI Article Synopsis

  • Vertebro-basilar dolichoectasia (VBD) is a rare and serious condition with an unclear cause, leading to a poor prognosis and high mortality rate.
  • A case study highlights how VBD was discovered in a patient experiencing altered mental status, with brain imaging revealing severe hydrocephalus due to third ventricle compression.
  • Despite surgical attempts to manage the condition, including placing an external ventricular shunt, the patient unfortunately died, underlining the challenges in treating VBD.

Article Abstract

Unlabelled: Vertebro-basilar dolichoectasia (VBD) is a rare pathology of unknown aetiology. Its clinical presentation is wide and prognosis is generally poor with a high mortality rate. Cerebral magnetic resonance imaging is the gold standard for diagnosis. We report an unusual case of intracranial dolichoectasia. VBD was revealed during investigation of a patient with altered mental status. CT brain imaging demonstrated severe obstructive hydrocephalus secondary to compression of the third ventricle. Management is always challenging and depends on the location and the mode of presentation. Our patient died despite surgical management with placement of an external ventricular shunt.

Learning Points: Vertebro-basilar dolichoectasia is a little known cause of altered mental status in elderly patients.An atypical presentation of vertebro-basilar dolichoectasia can mimic extensive cerebrovascular haemorrhage.The prognosis is poor despite prompt diagnosis and the surgical treatment of choice.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC9426960PMC
http://dx.doi.org/10.12890/2022_003436DOI Listing

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Article Synopsis
  • Vertebro-basilar dolichoectasia (VBD) is a rare and serious condition with an unclear cause, leading to a poor prognosis and high mortality rate.
  • A case study highlights how VBD was discovered in a patient experiencing altered mental status, with brain imaging revealing severe hydrocephalus due to third ventricle compression.
  • Despite surgical attempts to manage the condition, including placing an external ventricular shunt, the patient unfortunately died, underlining the challenges in treating VBD.
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Background: Symptomatic hydrocephalus due to vertebrobasilar dolichoectasia is a rare occurrence.

Case Description: We report a patient who presented with acute confusion and vomiting. Neuroimaging revealed elongated and tortuous basilar artery indenting and elevating the floor of third ventricle causing obstructive hydrocephalus.

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Background: The aim of this study was to analyse the morphometry of the intracranial segment of the vertebral artery in the context of clinical usefulness. The results were compared with published data available in full-text archived medical journals.

Materials And Methods: More than 100 digital subtraction angiography (DSA) and 3-dimensional (3D) angio-computed tomography (CT) examinations were used to measure the following parameters: the whole and partial length of V4 in characteristic anatomical points, the diameter in three places (on the level of foramen magnum, in point of exit to the posterior inferior cerebellar artery, and in the vertebro-basilar junction), the angle of connection to the vertebral arteries, and all anatomical variations including fenestration, duplication, dolichoectasia or absent artery.

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[Painful tic convulsif: Case series and literature review].

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December 2017

Departamento de Neurocirugía, Instituto Nacional de Neurología y Neurocirugía Dr. Manuel Velasco Suárez, Ciudad de México, México.

Background: The coexistence of hemifacial spasm and trigeminal neuralgia, a clinical entity known as painful tic convulsive, was first described in 1910. It is an uncommon condition that is worthy of interest in neurosurgical practice, because of its common pathophysiology mechanism: Neuro-vascular compression in most of the cases.

Objective: To present 2 cases of painful tic convulsive that received treatment at our institution, and to give a brief review of the existing literature related to this.

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We described a patient who had left trigeminal neuralgia by vertebro-basilar dolichoectasia, who underwent microvascular decompression separating the basilar artery of the trigeminal nerve by interposing a vascular graft piece. Symptoms resolved completely after surgery. Nine years later, he has a recurrence of facial pain associated with rapidly progressive brainstem compressive symptoms.

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