Wallenberg Syndrome: Two Case Reports Highlighting Vertebral Artery Dissection and Thrombophilia as Distinct Etiologies
Sara Remelhe Sá, Rita Pera, João Lagarteira, Lilia Castelo Branco, Cristiana Batouxas

TL;DR
Two case reports show different causes of Wallenberg syndrome, highlighting the need for accurate diagnosis and multidisciplinary care.
Contribution
The paper presents two distinct etiologies of Wallenberg syndrome: vertebral artery dissection and thrombophilia.
Findings
Case 1 showed vertebral artery dissection as the cause of Wallenberg syndrome.
Case 2 revealed thrombophilia-related infarction without dissection.
MRI was crucial for diagnosis, as CT scans were inconclusive.
Abstract
Wallenberg syndrome, or lateral medullary syndrome, is caused by ischemia of the posterolateral medulla, most often attributed to vertebral artery or posterior inferior cerebellar artery occlusion. The condition is characterized by heterogeneous sensory, cerebellar, and autonomic deficits induced by damage to multiple brainstem nuclei and tracts. Herein, we report two cases of Wallenberg syndrome associated with different etiological mechanisms. Case 1 involved a 55-year-old man with vertigo, diplopia, anisocoria with ipsilateral ptosis, and left-sided sensory deficits. Magnetic resonance imaging (MRI) revealed a 9-mm diffusion-restricted lesion in the right posterolateral medulla and signs of proximal intracranial vertebral artery dissection. Case 2 involved a 41-year-old man with vertigo, dysphonia, dysphagia, ipsilateral facial sensory loss, and contralateral body hypoalgesia. MRI…
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Taxonomy
TopicsCervical and Thoracic Myelopathy · Vestibular and auditory disorders · Aortic Disease and Treatment Approaches
