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2024, Number 07

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Med Int Mex 2024; 40 (07)

Wallenberg syndrome associated with spontaneous vertebral dissection

Hernández VLA, de Lera AM
Full text How to cite this article

Language: Spanish
References: 16
Page: 445-451
PDF size: 269.14 Kb.


Key words:

Vertebral artery, Vertebral artery dissection, Wallenberg syndrome, Stroke.

ABSTRACT

Background: Wallenberg syndrome is caused by infarction of the lateral and posterior portion of the inferior olivary nucleus of the medulla oblongata. Its diagnosis is usually a challenge, since it frequently manifests with non-specific symptoms or that overlap with a stroke of the anterior circulation.
Clinical case: A 48-year-old male patient, with no personal history of interest, who consulted for vertigo and instability. On examination he presented: left Horner’s syndrome, slight drooping of the left palate, left facial palsy, ataxia, left lateropulsion, hypoesthesia in the right hemibody. Cover test, cephalic imposed and HINTS test were negative. A computed tomography (CT) scan of the brain showed no alterations, and angio-CT of the supra-aortic trunks and circle of Willis showed loss of flow density of the left vertebral artery in its V3 and V4 segments. Subsequently, in brain magnetic resonance image (MRI) and MRI-angiography of the supra-aortic trunks and circle of Willis, acute infarct foci were observed in the left lateral region of the medulla oblongata and posterior and inferomedial region of the left cerebellar hemisphere, filiform flow in the left V3 and V4 segments.
Conclusions: Vertebral artery dissection is an important cause to consider and should be suspected in young patients.


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Med Int Mex. 2024;40