Intramedullary spinal cord ganglioglioma presenting with abnormal abdominal wall movement. Case report

Saeid Aslanabadi1, Ramin Azhough, Parviz Samad Motlagh

  • 1Department of Surgery, Neurosurgery, and Pathology, Tabriz University of Medical Sciences, Tabriz, Iran. ramin_azhough780@yahoo.com

Neurosurgical Focus
|January 7, 2005
PubMed

Insights

A rare intramedullary ganglioglioma caused a child's "belly dance" symptom. Surgical resection led to good recovery, though scoliosis progressed post-surgery.

Area of Science:

  • Pediatric Neurology
  • Neuro-oncology
  • Spinal Cord Tumors

Background:

  • Gangliogliomas are rare tumors, often found in the central nervous system.
  • Intramedullary spinal cord tumors are uncommon and can present with varied neurological deficits.
  • Early diagnosis and management are crucial for pediatric patients with spinal cord lesions.

Observation:

  • A 6-year-old girl presented with a unique, continuous abdominal wall movement termed "belly dance" since infancy.
  • This "belly dance" symptom persisted even during sleep, suggesting a neurological origin.
  • Magnetic resonance imaging (MRI) identified an intramedullary tumor with indistinct margins.

Findings:

  • The patient was diagnosed with an intramedullary ganglioglioma.
  • Surgical debulking of the tumor was performed.
  • Postoperative recovery was favorable, with resolution of the "belly dance" symptom.

Implications:

  • This case highlights the diverse and unusual presentations of intramedullary spinal cord tumors in children.
  • The "belly dance" symptom may serve as an early indicator for spinal cord pathology.
  • Long-term monitoring is essential due to the potential for delayed complications like scoliosis progression.

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