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Concomitant spinal dural arteriovenous fistula and nodular fasciitis in an adolescent: case report

BACKGROUND: Spinal dural arteriovenous fistula (SDAVF) usually occurs during the 4(th) to 6(th) decades of life, and adolescent SDAVF is rarely reported. SDAVF arising around a tumor is also rare, and reported tumors are mostly schwannoma and lipoma. CASE PRESENTATION: We reported a 16-year-old male...

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Detalles Bibliográficos
Autores principales: Chu, Chan-Lin, Lu, Yu-Jen, Lee, Tsong-Hai, Jung, Shih-Ming, Chu, Yu-Cheng, Wong, Ho-Fai
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8742378/
https://www.ncbi.nlm.nih.gov/pubmed/34998361
http://dx.doi.org/10.1186/s12887-021-03032-0
Descripción
Sumario:BACKGROUND: Spinal dural arteriovenous fistula (SDAVF) usually occurs during the 4(th) to 6(th) decades of life, and adolescent SDAVF is rarely reported. SDAVF arising around a tumor is also rare, and reported tumors are mostly schwannoma and lipoma. CASE PRESENTATION: We reported a 16-year-old male presented with progressive weakness and numbness of lower limbs for 3 months. A SDAVF was found, which was fed by right radicular arteries from segmental artery at L2 level and drained retrogradely into perimedullary veins. A concomitant spinal extradural nodular fasciitis at right L1/L2 intervertebral foramen was also noted. The SDAVF was completely obliterated by endovascular treatment and the tumor was debulked. The patient recovered well after the procedures. CONCLUSIONS: Our case report suggests SDAVF can occur in adolescent. The concomitant presence with a nodular fasciitis indicates that although it usually arises in subcutaneous tissue but can rarely form on the dura of spine.