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Diseases

Genetic and Rare Diseases Information Center (GARD)

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Fibrocartilaginous embolism


Other Names for this Disease
  • Embolism, fibrocartilaginous
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Tests & Diagnosis


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How is fibrocartilaginous embolism diagnosed?

Initially, all cases of fibrocartilaginous embolism (FCE) were discovered at autopsy. In 1991, the first diagnosis of FCE was made in a patient who survived. Although there are no formal diagnostic criteria for FCE in a living individual, a number of authors have suggested specific features that make the diagnosis likely. These include minor trauma before the event, absence of vascular risk factors, spinal cord imaging consistent with an evolving infarction, normal cerebrospinal fluid (CSF) analysis, and the exclusion of other possible causes.[1]
Last updated: 3/24/2011

References
  1. F. J. Mateena,b, P. A. Monradb, A. N. Leep Hunderfundb, C. E. Robertsonb and E. J. Sorenson. Clinically suspected fibrocartilaginous embolism: clinical characteristics, treatments, and outcomes. European Journal of Neurology. 2011; 18:218-225.