Annals of Indian Academy of Neurology
IMAGES IN NEUROLOGY
Year
: 2021  |  Volume : 24  |  Issue : 4  |  Page : 589-

A case of paroxysmal kinesigenic myoclonus with episodic piloerection


CJ Suresh Chandran, Anoop Sugunan, Joseph Shibu 
 Department of Neurology, Kerala Institute of Medical Sciences, Thiruvananthapuram, Kerala, India

Correspondence Address:
Dr. C J Suresh Chandran
Department of Neurology, Kerala Institute of Medical Sciences, Thiruvananthapuram, Kerala
India




How to cite this article:
Suresh Chandran C J, Sugunan A, Shibu J. A case of paroxysmal kinesigenic myoclonus with episodic piloerection.Ann Indian Acad Neurol 2021;24:589-589


How to cite this URL:
Suresh Chandran C J, Sugunan A, Shibu J. A case of paroxysmal kinesigenic myoclonus with episodic piloerection. Ann Indian Acad Neurol [serial online] 2021 [cited 2021 Nov 29 ];24:589-589
Available from: https://www.annalsofian.org/text.asp?2021/24/4/589/307431


Full Text



A 45-year-old lady presented with 3 weeks history of very brief episodic involuntary posturing on initiating movements. The episodes consisted of mild neck flexion with outstretching of both upper limbs lasting 1–2 s. She was fully conscious and there were no facial movements. These occurred exclusively on movement and had several episodes per day. They were absent in sleep. She also had short-lasting episodes of goosebumps all over body. She was fully conscious during these episodes of goosebumps which use to last 10-20 seconds. Clinical examination revealed episodic piloerection and mild episodic memory decline. A video EEG showed paroxysmal Kinesigenic myoclonus [Video 1]. Interictal EEG was normal and ictal EEG showed EMG artifacts only. MRI brain showed limbic encephalitis [Figure 1]. Serum and CSF anti LGI1 antibody was positive. She was treated with pulse methylprednisolone followed by oral prednisolone, azathioprine and oxcarbazepine. She responded in 3 weeks, both piloerection and involuntary movements disappeared. Medications were tapered off after 1 year and she is in remission at 2-year follow-up.{Figure 1}

Prototypical paroxysmal dyskinesia in LGI1 encephalitis is facio brachial dystonic seizure (FBDS).[1] Paroxysmal kinesogenic dyskinesia has been rarely described in anti-LGI1 encephalitis and other autoimmune encephalitis.[1],[2] Pilomotor seizures are unusual autonomic seizures usually associated with temporal lobe epilepsy (TLE). Rarely frontal and hypothalamic origin also have been reported. Unilateral piloerection may indicate an ipsilateral focus, whereas bilateral piloerection does not have any clear lateralizing value.[3] Association of Piloerection to autoimmune encephalitis is recently recognized, anti-LGI1 encephalitis being the commonest.[1],[4]

Declaration of patient consent

The authors certify that they have obtained all appropriate patient consent forms. In the form the patient(s) has/have given his/her/their consent for his/her/their images and other clinical information to be reported in the journal. The patients understand that their names and initials will not be published and due efforts will be made to conceal their identity, but anonymity cannot be guaranteed.

Financial support and sponsorship

Nil.

Conflicts of interest

There are no conflicts of interest.

References

1Balint B, Vincent A, Meinck H-M, Irani SR, Bhatia KP. Movement disorders with neuronal antibodies: Syndromic approach, genetic parallels and pathophysiology. Brain 2018;141:13-36.
2Rahangdale R, Scott T, Leichliter T, Baser S, Valeriano J. A case of paroxysmal dystonia associated with LGI-1 antibody encephalitis. Clin Neurol Neurosurg 2019;186:105508.
3Loddenkemper T, Kellinghaus C, Gandjour J, Nair DR, Najm IM, Bingaman W, et al. Localising and lateralising value of ictal piloerection. J Neurol Neurosurg Psychiatry 2004;75:879-83.
4Rocamora R, Becerra JL, Fossas P, Gomez M, Vivanco-Hidalgo RM, Mauri JA, et al. Pilomotor seizures: An autonomic semiology of limbic encephalitis? Seizure 2014;23:670-3.