Dancing eye syndrome as first symptom of neuroblastoma

Dancing eye syndrome as first symptom of neuroblastoma

Authors

  • Cristina Venturelli Post-Graduate School of Pediatrics University of Modena and Reggio Emilia
  • Azzurra Guerra Pediatric Unit, Department of Medical and Surgical Sciences
  • Paolo Paolucci Post-Graduate School of Pediatrics Pediatric Unit University of Modena and Reggio Emilia
  • Lorenzo Iughetti Post-Graduate School of Pediatrics Pediatric Unit University of Modena and Reggio Emilia

Keywords:

Opsoclonus-Myoclonus Syndrome, dancing eye syndrome, neuroblastoma, paraneoplastic neurologic disorder

Abstract

Background: “Dancing eye syndrome”, also called Kinsbourne syndrome or Opsoclonus-Myoclonus-Ataxia Syndrome (OMS) is a rare neurological disorder that in children is frequently associated to occult, low-grade neuroblastoma (NB) (>50% of the cases). OMS may also be triggered by infections and it is often associated to developmental impairment and disability.

Case presentation: We discuss the case of a 16 months old female with acutely onset of OMS associated to occult stage III NB.

Conclusions: OMS represents a diagnostic challenge for pediatric clinicians. The suspect of OMS imposes the search for an occult NB in order to promptly treat a life-threatening event like tumor and to prevent the neurological sequels linked to OMS.

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Published

01-09-2013

Issue

Section

CASE REPORTS

How to Cite

1.
Venturelli C, Guerra A, Paolucci P, Iughetti L. Dancing eye syndrome as first symptom of neuroblastoma. Acta Biomed [Internet]. 2013 Sep. 1 [cited 2024 Jul. 27];84(2):162-6. Available from: https://mattioli1885journals.com/index.php/actabiomedica/article/view/2726