Poliomyelitis-like syndrome

Case contributed by Christine Goh
Diagnosis probable

Presentation

4 days weakness and hyporeflexia on background of diarrheal illness.

Patient Data

Age: 35 years
Gender: Male

MRI spinal cord

mri

Abnormal T2 hyperintensity involving most of the length of the cord has bilaterally symmetric appearance, with signal abnorrmality centered on the anterior horns.  There was no pathological enhancement within the cord, and no abnormally enhancing nerve roots.

Minimal disc protrusions at a few levels do not result in spinal canal stenosis or cord compression.  No abnormal vascular flow voids or areas of susceptibility artefact within the cord.

In the context of febrile/diarrheal illness, an infective or postinfectious etiology was considered likely, and the combination of acute flaccid paralysis with anterior horn changes favors poliomyelitis-like syndrome.

The MRI findings were not consistent with the initial clinical diagnosis of Guillain-Barre syndrome, which is characterized by normal cord appearance, with variable nerve root enhancement.

Grey matter signal abnormality with anterior horn predominance can be seen in cord ischemia, however this would usually have a more abrupt onset of neurological deficit.

MRI brain

mri

MR imaging of the brain  demonstrated T2 and FLAIR signal abnormality centered on the dentate nuclei and circumferentially involving the brainstem.  There was no basal ganglia or thalamic involvement, and no parenchymal or leptomeningeal enhancement.

Findings are compatible with a rhombencephalitis.

Case Discussion

CSF analysis demonstrated a mild lymphocytosis with normal protein level.

Poliomyelitis-like syndrome (resulting in anterior horn syndrome) is an infective myelitis by pathogens which selectively involve the anterior horn cells to cause an acute flaccid paralysis.  

The archetypical infective agent is poliomyelitis, although due to high rates of vaccination it is now more common for outbreaks of enterovirus 71 or West Nile virus to be implicated.  Other picornaviruses and flaviviruses such as coxsackie A and B viruses, Japanese encephalitis virus and Murray Valley virus are rare causes of poliomyelitis-like syndrome, with encephalitic presentations far more common than anterior horn cell involvement.

The typical MRI appearance is long segment T2 hyperintensity centered on the anterior horns, usually non enhancing.

There may also be imaging findings related to concurrent encephalitis.  Bilateral thalamic and brainstem involvement is the classic distribution of findings in encephalitis due to flaviviruses such as Japanese encephalovirus and West Nile virus.

How to use cases

You can use Radiopaedia cases in a variety of ways to help you learn and teach.

Creating your own cases is easy.

Updating… Please wait.

 Unable to process the form. Check for errors and try again.

 Thank you for updating your details.