Superficial siderosis of the central nervous system associated with incomplete dural closure following posterior fossa surgery: report of 3 cases

被引:9
|
作者
Kumar, Ravi [1 ]
Jacob, Jeffrey T. [1 ]
Welker, Kirk M. [2 ]
Cutrer, Fred M. [3 ]
Link, Michael J. [1 ]
Atkinson, John L. D. [1 ]
Wetjen, Nicholas M. [1 ]
机构
[1] Mayo Clin, Dept Neurosurg, Rochester, MN 55905 USA
[2] Mayo Clin, Dept Radiol, Rochester, MN 55905 USA
[3] Mayo Clin, Dept Neurol, Rochester, MN 55905 USA
关键词
superficial siderosis; posterior fossa; sensorineural hearing loss; pseudomeningocele; OF-THE-LITERATURE; LOCALIZATION; MYELOGRAPHY; CNS;
D O I
10.3171/2014.12.JNS141920
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
This report reviews a series of 3 patients who developed superficial siderosis following posterior fossa operations in which dural closure was incomplete. In all 3 patients, revision surgery and complete duraplasty was performed to halt the progression of superficial siderosis. Following surgery, 2 patients experienced resolution of their CSF xanthochromia while 1 patient had reduced CSF xanthochromia. In this paper the authors also review the etiology, pathophysiology, diagnosis, and treatment of this condition. The authors suggest that posterior fossa dural patency and pseudomeningocele are risk factors for the latent development of superficial siderosis and recommend that revision duraplasty be performed in patients with posterior fossa pseudomeningoceles and superficial siderosis to prevent progression of the disease.
引用
收藏
页码:1326 / 1330
页数:5
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