Shapiro G S, Millett P J, DiCarlo E F, Mintz D N, Gamache F W, Rawlins B A
Department of Orthopaedics, Hospital for Special Surgery, New York, NY 10021, USA.
Skeletal Radiol. 2001 May;30(5):290-4. doi: 10.1007/s002560000297.
We report the case of a 39-year-old woman with adolescent idiopathic scoliosis presenting with myelopathy secondary to a spinal epidural hemangioma. MRI showed an epidural soft tissue mass within the spinal canal between T5 and T9 with severe spinal cord compression. Symptoms had a temporal relationship to her pregnancy. Surgical removal of the epidural hemangioma rapidly relieved her symptoms and neurologic deficits. Follow-up examination 2 years later demonstrated normal motor and sensory function, without any neurologic sequelae or progression of deformity.
我们报告了一例39岁患有青少年特发性脊柱侧凸的女性病例，该患者因脊髓硬膜外血管瘤继发脊髓病。磁共振成像（MRI）显示在T5至T9之间的椎管内有一个硬膜外软组织肿块，伴有严重的脊髓压迫。症状与她的妊娠存在时间上的关联。手术切除硬膜外血管瘤迅速缓解了她的症状和神经功能缺损。2年后的随访检查显示运动和感觉功能正常，没有任何神经后遗症或畸形进展。
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