A novel association between RASA1 mutations and spinal arteriovenous anomalies

AJNR Am J Neuroradiol. 2010 Apr;31(4):775-9. doi: 10.3174/ajnr.A1907. Epub 2009 Dec 10.

Abstract

Background and purpose: CM-AVM is a recently recognized autosomal dominant disorder associated with mutations in RASA1. Arteriovenous lesions have been reported in the brain, limbs, and the face in 18.5% of patients. We report a novel association between RASA1 mutations and spinal arteriovenous anomalies.

Materials and methods: In a collaborative study, 5 index patients (2 females, 3 males) with spinal AVMs or AVFs and cutaneous multifocal capillary lesions were investigated for the RASA1 gene mutation.

Results: All 5 patients were found to have RASA1 mutation (2 de novo, 3 familial), and all had multifocal capillary malformations at birth. Neurologic deficits developed at ages ranging from infancy to early adulthood. All spinal anomalies (2 AVMs at the conus, 1 AVM at the lumbosacral junction, and 1 cervical and 1 cervicothoracic AVF) were complex, extensive, and fast-flow lesions. All patients required treatment based on the clinical and/or radiologic appearance of the lesions.

Conclusions: To our knowledge, an association of RASA1 mutation and spinal AVM/AVF has not been described. MR imaging screening of patients with characteristic CMs and neurologic symptoms presenting at a young age may be useful in detecting the presence of fast-flow intracranial or intraspinal arteriovenous anomalies before potentially significant neurologic insult has occurred.

MeSH terms

  • Adult
  • Angiography
  • Arteriovenous Malformations / diagnosis
  • Arteriovenous Malformations / genetics*
  • Arteriovenous Malformations / therapy
  • Child
  • Child, Preschool
  • Chromosome Aberrations*
  • Combined Modality Therapy
  • DNA Mutational Analysis*
  • Embolization, Therapeutic
  • Female
  • Follow-Up Studies
  • Genes, Dominant / genetics*
  • Genotype
  • Hemangioma, Capillary / diagnosis
  • Hemangioma, Capillary / genetics
  • Hemangioma, Capillary / therapy
  • Humans
  • Infant
  • Magnetic Resonance Imaging
  • Male
  • Microsurgery
  • Neoplasms, Multiple Primary / diagnosis
  • Neoplasms, Multiple Primary / genetics
  • Neoplasms, Multiple Primary / therapy
  • Neurologic Examination
  • Postoperative Complications / diagnosis
  • Skin Neoplasms / diagnosis
  • Skin Neoplasms / genetics
  • Skin Neoplasms / therapy
  • Spinal Cord / blood supply*
  • Spinal Cord Compression / diagnosis
  • Spinal Cord Compression / genetics
  • Spinal Cord Compression / therapy
  • Young Adult
  • p120 GTPase Activating Protein / genetics*

Substances

  • p120 GTPase Activating Protein