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Cerebrofacial Arteriovenous Metameric Syndrome (CAMS) Type II

  • Background:
    • CVMS is a term that encompasses craniofacial AVM syndromes and classifies them according to the location of AVMs. CAMS is classified into 3 subgroups:
      • CAMS I: medial prosencephalic group with involvement of nose and hypothalamus
      • CAMS II: lateral prosencephalic group with involvement of occipital lobe, optic chiasma, optic tract, thalamus, retina, and maxilla
      • CAMS III: rhombencephalic group with involvement of cerebellum, pons, and mandible
    • Our case has a rare variant of CAMS II, which involves the temporal lobe as well.
  • Clinical Presentation:
    • Most cases present in childhood and adolescence, even though the brain and facial AVMs may be present since birth.
    • The most common presenting symptoms are progressive visual loss, progressive neurologic deficits, and bleeding from gums/teeth.
    • Cosmetic complaints like facial asymmetry and proptosis are also common.
    • Seizures have also been reported as presenting symptoms.
  • Key Diagnostic Features:
    • Diagnosis involves thorough clinical evaluation, review of detailed patient history, and identification of characteristic findings, especially ocular findings.  
    • CT with contrast and/or brain MRI show dilated vessels or flow voids.
    • The AVM nidus is usually diffuse and extends along the optic nerve into the orbit. 
  • Differential Diagnosis:
    • Cerebral proliferative angiopathy: characterized by the presence of normal brain parenchyma interspersed throughout the tangle of vessels that corresponds to the nidus; no facial involvement
  • Treatment:
    • As the nidus is diffuse, a complete cure is usually not possible.
    • Treatment strategies include palliative treatment with targeted embolization of the higher flow compartments or the angioarchitectural weak points.
August 24, 2017

A 24-year-old man with known vascular anomaly and left facial and arm spasms for the past 2 weeks, worsening over the past 4 days

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Print ISSN: 0195-6108 Online ISSN: 1936-959X

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