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Peer-reviewed veterinary case report

Snake-eye myelopathy in dogs seen on spinal MRI scans

By Rossmeisl, John H et al.·Published in Frontiers in veterinary science·2019·Department of Small Animal Clinical Sciences, United States·View original on PubMed

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Original publication title: Canine Snake-Eye Myelopathy: Clinical, Magnetic Resonance Imaging, and Pathologic Findings in Four Cases.

Species:
dog

Plain-English summary

A 7-year-old Labrador Retriever was brought in for weakness and difficulty moving its front legs, which was diagnosed as a central cord syndrome due to spinal cord compression. MRI scans revealed a unique pattern known as "snake-eye" myelopathy, indicating severe damage to the spinal cord. Despite various treatments, the dog's condition worsened, leading to paralysis in its front limbs while other functions remained intact for some time. Unfortunately, the prognosis for recovery of movement in the front legs was poor, and the dog continued to show signs of deterioration.

People also search for: dog front leg weakness · snake-eye myelopathy in dogs · dog spinal cord compression treatment · Labrador Retriever paralysis symptoms

Abstract

Intramedullary signal change (ISC) is a non-specific finding that is frequently observed on magnetic resonance imaging (MRI) examinations of the canine spinal cord. ISC can represent a variety of primary pathological processes such as neoplasms or myelitides or secondary changes such as edema, cysts, gliosis, or myelomalacia. An unusual phenotype of ISC is the "snake-eye" myelopathy (SEM), which refers to bilaterally symmetric T2 hyperintensities preferentially affecting the ventral horn gray matter on transverse MR images, which resemble a pair of snake's eyes. The pathophysiology of SEM is poorly understood in humans, and this imaging finding may be associated with cervical spondylotic myelopathy, spinal cord ischemia, ossification of the posterior longitudinal ligament, amyotrophic lateral sclerosis, and Hirayama disease. Here we describe four dogs with cervical MRI examinations consistent with an SEM-like phenotype. All dogs initially presented with a central cord syndrome or tetraparesis referable to a C6-T2 neuroanatomic localization, which was attributed to disc-associated spinal cord compression in three cases, while one dog had the SEM-like phenotype with no identifiable etiology. Once the SEM-like phenotype was present on MRI examinations, dogs demonstrated insidious clinical deterioration despite therapeutic interventions. Deterioration was characterized by lower motor neuron weakness and neurogenic muscle atrophy progressing to paralysis in the thoracic limbs, while neurological functions caudal to the level of the SEM-like lesion remained largely preserved for months to years thereafter. Neuropathological features of the SEM-like phenotype include multisegmental cavitations and poliomyelomalacia of laminae VI-IX of the caudal cervical spinal cord, although the lesion evolved into pan-necrosis of gray matter with extension into the adjacent white matter in one case with an 8 years history of progressive disease. Although the pathophysiology of SEM remains unknown, the topographical distribution and appearance of lesions is suggestive of a vascular disorder. As the SEM-like phenotype was uniformly characterized by longitudinally and circumferentially extensive neuronal necrosis, results of this small case series indicate that dogs with clinical signs of central cord syndrome and the SEM-like phenotype involving the cervicothoracic intumescence on MR examinations have a poor prognosis for the preservation or recovery of thoracic limb motor function.

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Original publication on PubMed: https://pubmed.ncbi.nlm.nih.gov/31334255/