TY - JOUR
T1 - Mystery Case
T2 - Brown-Séquard syndrome caused by idiopathic spinal cord herniation
AU - Fonoff, Erich Talamoni
AU - Contreras Lopez, William Omar
AU - Teixeira, Manoel Jacobsen
N1 - Publisher Copyright:
© 2016 American Academy of Neurology.
PY - 2016/7/26
Y1 - 2016/7/26
N2 - A 48-year-old man developed numbness in the left leg, which progressed gradually to paresis and urinary incontinence. Neurologic examination revealed a left Brown-Sequard syndrome with leg paresis, mild spasticity, reduced proprioception, and contralateral thermal and painful hypoesthesia below T6. MRI revealed a thoracic spinal cord herniation (SCH) (figure). Idiopathic SCH is relatively rare. Pathogenesis involves a dura mater defect (see video on the Neurology® Web site at Neurology.org); herniation develops over a progressive pressure gradient through the dural fissure. 2 Surgical reduction is typically performed if symptoms progress, but mild symptoms may be eligible for conservative treatment and monitoring. Surgical spinal reduction and dural repair usually reverses neurologic deficits.
AB - A 48-year-old man developed numbness in the left leg, which progressed gradually to paresis and urinary incontinence. Neurologic examination revealed a left Brown-Sequard syndrome with leg paresis, mild spasticity, reduced proprioception, and contralateral thermal and painful hypoesthesia below T6. MRI revealed a thoracic spinal cord herniation (SCH) (figure). Idiopathic SCH is relatively rare. Pathogenesis involves a dura mater defect (see video on the Neurology® Web site at Neurology.org); herniation develops over a progressive pressure gradient through the dural fissure. 2 Surgical reduction is typically performed if symptoms progress, but mild symptoms may be eligible for conservative treatment and monitoring. Surgical spinal reduction and dural repair usually reverses neurologic deficits.
UR - http://www.scopus.com/inward/record.url?scp=84980374175&partnerID=8YFLogxK
U2 - 10.1212/WNL.0000000000002886
DO - 10.1212/WNL.0000000000002886
M3 - Articulo en revista no especializada
C2 - 27462042
AN - SCOPUS:84980374175
SN - 0028-3878
VL - 87
SP - e34
JO - Neurology
JF - Neurology
IS - 4
ER -