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[A case of sinus pericranii manifesting as a parietal midline mass]

Y Akiba1, M Ebara, H Nakazaki

  • 1Department of Neurosurgery, Jikei University School of Medicine, Kashiwa Hospital, 163-1 Kashiwashita, Kashiwa-city, Chiba 277-8567, Japan.

Insights

This case report details a sinus pericranii in a child, a rare scalp mass. Successful treatment involved mass removal and bone defect closure without craniotomy.

Area of Science:

  • Neurosurgery
  • Pediatric Surgery
  • Vascular Malformations

Background:

  • Sinus pericranii is a rare congenital vascular malformation characterized by a venous communication between the intracranial dural sinuses and the pericranial veins.
  • These lesions typically present as a soft, compressible scalp mass that enlarges when the patient is in a dependent position.

Observation:

  • A 5-year-old boy presented with a midparietal scalp mass present for 3 years, which varied in size with posture.
  • Magnetic resonance imaging (MRI) revealed a mass with mixed T1 and high T2 signal intensity, and irregular enhancement after Gd-DTPA administration.
  • Cerebral angiography and direct mass injection failed to demonstrate communication with the superior sagittal sinus, while 3D-CT identified small underlying bone defects.

Findings:

  • Surgical exploration confirmed the mass was located between the galea aponeurotica and periosteum, with a minor communication to an emissary vein.
  • Pathological examination identified the mass as a lobular cyst with an endothelial lining.
  • The absence of significant dural sinus communication was noted.

Implications:

  • This case highlights a minimally communicating sinus pericranii successfully treated via surgical excision and closure of cranial bone defects with bone wax.
  • The findings suggest that craniotomy may not be necessary for treating certain sinus pericranii cases, offering a less invasive surgical approach.
  • This approach potentially reduces surgical morbidity in pediatric patients with this rare vascular anomaly.

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