Pediatric triad of craniofacial fibrous dysplasia, Chiari malformation type I and syringomyelia: a case report - Takeaways - MDSpire

Pediatric triad of craniofacial fibrous dysplasia, Chiari malformation type I and syringomyelia: a case report

  • By

  • Yaxiong Li

  • Jianfeng Liu

  • Jian Guan

  • Conghui Li

  • January 3, 2026

  • 0 min

Share

  • 1

    Fibrous dysplasia (FD) is a rare benign bone lesion causing skeletal deformities and can lead to complications like Chiari malformation type I (CM1) and syringomyelia (SM).

  • 2

    A 16-year-old girl with craniofacial fibrous dysplasia, CM1, and SM experienced unsteady gait and dizziness, with significant imaging findings of cranial abnormalities.

  • 3

    Surgical intervention involved decompression of the foramen magnum, which successfully alleviated symptoms and reduced the severity of syringomyelia postoperatively.

  • 4

    Histopathological examination confirmed the diagnosis of fibrous dysplasia, characterized by irregular bony trabeculae within a fibrous stroma.

  • 5

    The case highlights the relationship between craniofacial fibrous dysplasia, Chiari malformation, and syringomyelia, emphasizing the importance of surgical treatment.

Original Source(s)

Related Content