Related Experiment Videos

[Cranial fasciitis of childhood]

T Koyama1, N Nakamura, T Wada

  • 1Department of Neurosurgery, Jikei University School of Medicine, Tokyo, Japan.

No to Shinkei = Brain and Nerve
|December 1, 1991
PubMed

Insights

This report details a rare cranial fasciitis case in a child, a benign scalp tumor originating from deep fascia or periosteum. It highlights the importance of considering this condition in pediatric scalp lesions.

Area of Science:

  • Pediatric Neurosurgery
  • Surgical Pathology
  • Oncology

Background:

  • Cranial fasciitis is a rare, benign subcutaneous tumor of the head, originating from deep fascia or cranial periosteum.
  • First described in 1990, it is characterized by fibroblast proliferation and often presents in infants and children.
  • It shares similarities with nodular fasciitis but is specifically associated with the skull bone.

Observation:

  • A case of cranial fasciitis in a 1-year-old boy involving the temporoparietal bone is presented.
  • The tumor exhibited rapid, painless growth in the scalp, reaching a mean size of 2.5-3cm.
  • In some cases, cranial fasciitis can lead to destruction of the skull tables and adherence to the dura mater.

Findings:

  • Pathological findings reveal a proliferation of fibroblasts, consistent with a benign neoplastic process.
  • Cranial fasciitis is considered a variant of nodular fasciitis due to similar clinical and pathological features.
  • This condition requires differentiation from other pediatric scalp lesions.

Implications:

  • Neurosurgeons must include cranial fasciitis in the differential diagnosis of firm scalp lesions in children.
  • Increased awareness can lead to earlier and more accurate diagnosis of this rare condition.
  • This case report contributes to the limited global literature and is the first documented instance in Japan.

Related Concept Videos