Video Abstracts

Isolated Propriospinal Myoclonus as a Presentation of Cervical Myelopathy

Authors: {'first_name': 'Paula', 'last_name': 'Marrero-Gonz\xc3\xa1lez'},{'first_name': 'Berta', 'last_name': 'Pascual-Sedano'},{'first_name': 'Alejandro', 'last_name': 'Mart\xc3\xadnez-Dome\xc3\xb1o'},{'first_name': 'L. Estefan\xc3\xada', 'last_name': 'D\xc3\xadaz-Polo'},{'first_name': 'Esther', 'last_name': 'Granell'},{'first_name': 'Rodrigo', 'last_name': 'Rodr\xc3\xadguez'},{'first_name': 'Alexandre', 'last_name': 'Gironell'},{'first_name': 'Daniel', 'last_name': 'Guisado-Alonso'}


Background: Propriospinal myoclonus is an infrequent type of hyperkinetic movement that can be commonly idiopathic but also may occur after spinal cord lesions.

Phenomenology Shown: We describe an 8-year-old female showing repetitive flexor and extensor arrhythmic brief jerks of the trunk, compatible with propriospinal myoclonus secondary to cervical myelopathy.

Educational Value: Isolated propriospinal myoclonus may be the clinical sign that leads to the diagnosis of incipient myelopathy.

Keywords: Clinical neurology examinationmyoclonuspropriospinal myoclonusspinal cordArnold–Chiarisickle-cell disease 
 Accepted on 11 Oct 2018            Submitted on 12 Aug 2018

We present an 8-year-old girl with sickle cell disease (SCD) who was referred to our hospital because of bone infarctions. The patient developed bone pain three weeks before the admission and a bone scintigraphy showed bone infarctions in D9-L3 vertebral bodies. Hyperhydration, hydroxyurea and analgesia with non-steroidal anti-inflammatory drugs and opioid derivatives were initiated. The patient did not have other medical conditions.

Two months before admission, the patient presented with sudden involuntary movements consisting of repetitive flexor and extensor arrhythmic and anarchic brief jerks of the trunk (Video 1). These jerks were involuntary; the patient could not control them. The movements appeared spontaneously but also were stimulus sensitive, triggered by a gentle touch to the scalp around the ears. The jerks were painless, extended caudally, increased slightly when supine, were absent during sleep, and had no facial involvement. The rest of the neurological examination was normal. She did not complain of headaches spontaneously, but when she was asked the patient described a mild oppressive occipital headache in the last 4–5 months that did not get worse with Valsalva maneuvers. Surface electromyography was performed in the rectus abdominis and elbow flexor and extensor muscles, revealing arrhythmic bursts of >100 ms length and rostrocaudal conduction with axial muscle predominance and involvement of the distal segment and other spinal segments. Conduction velocities were not measured. Reticular myoclonus was ruled out because the absence of facial involvement that indicated caudorostral conduction and segmental myoclonus, which, in contrast to this case, is usually confined to one or few contiguous myotomes and the jerks are commonly rhythmic and not sensitive to stimulus. Therefore clinical phenomenology and electrophysiologic features were suggestive of propriospinal myoclonus.1,2

Video 1 

Propriospinal Myoclonus. Sudden and involuntary movements consisting in repetitive flexor and extensor arrhythmic and anarchic brief jerks of the trunk. The movements are spontaneous, painless and with no facial involvement.

Cervical C1–C2 myelopathy due to Arnold–Chiari malformation (ACM) type 1 was evidenced by magnetic resonance imaging (MRI) (Figure 1). Cerebral MRI did not show any ischemic lesions and the neurosonological study did not indicate increased risk of stroke. Electroencephalography was normal. Toxic–metabolic causes were ruled out. Suboccipital craniectomy and cervical laminectomy of the C1 posterior arch were performed. A few days after neurosurgical decompression of the foramen magnum, the myoclonus disappeared. The temporal relationship of clinical improvement with surgery was clear; there was no evidence of vaso-oclusion that caused ischemic damage to the central nervous system and the other conditions remained unchanged: the painful bone infarction persisted and the same analgesics continued to be administered. Consequently, in this case propriospinal myoclonus was probably secondary to structural cervical myelopathy because of ACM.

Figure 1 

Magnetic Resonance Imaging (MRI) Findings. Short tau inversion recovery sequence of MRI showing high signal intensity in the cervical spine at the C1–C2 level corresponding to spinal cord compression due to herniation of the cerebellar tonsils through the foramen magnum (Arnold–Chiari type I malformation).

ACM does not have a higher prevalence in patients with SCD, nevertheless it should be considered in the differential diagnosis of neurological symptoms in these patients.3

Finally, we would like to emphasize that isolated propriospinal myoclonus may be the clinical sign that leads to the diagnosis of incipient myelopathy. A broad study must be done in order to rule out secondary etiologies when we face patients with this clinical presentation.


1 Funding: None. 

2 Financial Disclosures: None. 

3 Conflicts of Interest: The authors report no conflict of interest. 

4 Ethics Statement: All patients that appear on video have provided written informed consent; authorization for the videotaping and for publication of the videotape was provided. 


The authors wish to thank Carla Temprano for editing the video and James Shaw for reviewing the English.


  1. Roze, E Bounolleau, P Ducreux, D Cochen, V Leu-Semenescu, S Beaugendre, Y et al. (2009). Propriospinal myoclonus revisited: clinical, neurophysiologic, and neuroradiologic findings. Neurology 72: 1301–1309, DOI: [PubMed]  

  2. van der Salm, SM Erro, R Cordivari, C Edwards, MJ Koelman, JHTM van den Ende, T et al. (2014). Propriospinal myoclonus: clinical reappraisal and review of literature. Neurology 83: 1862–1870, DOI: [PubMed]  

  3. Jordan, LC McKinstry III, RC Kraut, MA Ball, WS Vendt, BA Casella, JF et al. (2010). Incidental findings on brain magnetic resonance imaging of children with sickle cell disease. Pediatrics 126: 53–61. [PubMed]