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Froin's syndrome


FieldValue
nameFroin's syndrome
imageEpendymoma.png
captionEpendymoma of the cervical spine, completely obscurating the spinal canal
image_size160 px

Froin's syndrome is the coexistence of xanthochromia, high protein level and marked coagulation of cerebrospinal fluid (CSF). It is caused by meningeal irritation (e.g. during spinal meningitis) and CSF flow blockage by tumour mass or abscess. Stagnation of the CSF within the thecal sac facilitates exudation from the tumour itself and activation of coagulation factors. A clinical test formerly used for evaluation of spinal stenosis is Queckenstedt's maneuver. Nowadays, a magnetic resonance imaging is used for identification of CSF flow obstruction. It often shows the prolongation of T1 and T2 signal in CSF caudal to a level of block. This phenomenon is named after Georges Froin (1874–1932), a French physician who first described it.

References

References

  1. Govindarajan, R. (August 2012). "Froin's syndrome: an uncommon mimicker of Guillain–Barre syndrome.". European Spine Journal.
  2. Mirza, S. (May 2008). "Froin's syndrome revisited, 100 years on. Pseudo-Froin's syndrome on MRI.". Clinical Radiology.
  3. {{WhoNamedIt. synd. 1482. Froin's syndrome
  4. Froin G. ''Inflammations méningées avec chromatique, fibrineuse et cytologique du liquide céphalo-rachidien''. Gazette des hôpitaux, Paris 1903; 76:1005–1006.
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