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Updated: Aug 12, 2025
Induction of Paralysis and Visual System Injury in Mice by T Cells Specific for Neuromyelitis Optica Autoantigen Aquaporin-4
Published on: August 21, 2017
Paroxysmal painful tonic spasms in neuromyelitis optica spectrum disorder
Shoena Lucas1, Patrice H Lalive1,2, Agustina M Lascano1,2
1Faculty of Medicine, University of Geneva, Geneva, Switzerland.
Background:
Recently, an association between painful tonic spasms (PTS) and Neuromyelitis Optica Spectrum Disorder (NMOSD) was established.
Objective:
To describe the clinical characteristics of PTS in NMOSD based on a video recording and to provide a literature review on the topic.
Methods:
We report a case of a 38 years-old woman with a diagnosis of NMOSD and positive aquaporin-4 IgG antibody status who developed PTS five weeks after an episode of longitudinal extensive transverse myelitis (LETM).
Results:
Repetitive, brief, and painful episodes of muscle contraction were observed on the patient's left hand, spreading to the left arm, and then extending to the four limbs. While pregabalin and topiramate had no influence on these episodes, the patient responded to carbamazepine (CBZ), without symptom recurrence after one year.
Conclusions:
PTS in association with LETM can be considered typical for NMOSD. Although the exact mechanism is unknown, ephaptic transmission after spinal cord damage and excitatory soluble factors released during acute inflammation responses are sought to be involved. Symptomatic treatment with CBZ achieved remission of spams in our case.
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