Cargando…

Spontaneous regression of extradural high-flow vascular malformation in spinal arteriovenous metameric syndrome (SAMS): A unique case report

BACKGROUND: Spinal arteriovenous metameric syndrome (SAMS) is a rare nonhereditary genetic vascular disorder, involving multiple layers of tissues in the same metameric level. Spontaneous regression of SAMS has never been reported in the medical literature. CASE DESCRIPTION: A 42-year-old woman pres...

Descripción completa

Detalles Bibliográficos
Autores principales: Iampreechakul, Prasert, Chuntaroj, Songpol, Wattanasen, Yodkhwan, Hangsapruek, Sunisa, Lertbutsayanukul, Punjama, Siriwimonmas, Somkiet
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Scientific Scholar 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10246388/
https://www.ncbi.nlm.nih.gov/pubmed/37292406
http://dx.doi.org/10.25259/SNI_4_2023
Descripción
Sumario:BACKGROUND: Spinal arteriovenous metameric syndrome (SAMS) is a rare nonhereditary genetic vascular disorder, involving multiple layers of tissues in the same metameric level. Spontaneous regression of SAMS has never been reported in the medical literature. CASE DESCRIPTION: A 42-year-old woman presented with intermittent low back pain for 6 months. Magnetic resonance imaging of the thoracolumbar spine incidentally found clusters of spinal vascular malformations involving spinal cord, vertebral bodies, epidural space, and paraspinal muscles. There was no sign of venous congestion. Magnetic resonance angiography and spinal angiography revealed intradural spinal cord arteriovenous malformation (SCAVM) at the level of T10-11 and extradural high-flow osseous arteriovenous fistula. Due to asymptomatic SAMS and a high risk of anterior spinal arterial compromise during treatment, conservative treatment was considered in our patient. Spinal angiography obtained 8 years after initial angiography demonstrated significant regression of extradural component of SAMS and stable intradural SCAVM. CONCLUSION: We describe a unique case of SAMS with spontaneous regression of extradural component during a long-term observation period.