This case demonstrates imaging from a patient with clinically established amyotrophic lateral sclerosis (ALS). The diagnosis of classic ALS was established upon meeting the Escorial criteria for clinically definite ALS ¹:

1. signs of upper motor neuron damage (spastic pareses progredient over time, hyperreflexia) in >3 regions
2. signs of lower motor neuron damage (muscle atrophy, fibrillations/fasciculations in extremities and the tongue, and bulbar paresis (dysarthria, pathological laughter))
3. absence of other causes for upper or lower motor neuron damage (e.g. brain MRI as above, spinal canal stenosis was excluded by imaging (not included in this case), EMG was normal, blood and CSF tests were unremarkable)

This case shows two typical MRI signs of ALS:

• T2 hyperintensity in the corticospinal tracts
• motor band sign

​It is important to note that these radiological signs are rather unspecific and ALS remains a clinical diagnosis. Further both of these features are frequently seen subtly in 3 T imaging in healthy individuals and thus an appreciation for a 'normal' degree of signal in the corticospinal tract is essential.

In the four years since these images were obtained, the patient's spastic tetraparesis deteriorated, there was progressive atrophy of the extremities and additional troubles breathing. The ALS-FRS (Amyotrophic Lateral Sclerosis Functional Rating Scale) deteriorated from 38 to 19 within those 4 years.