Spinal arteriovenous malformation associated with spinal metameric syndrome: a treatable cause of long-term paraplegia? Case report

被引:11
作者
Linfante, Italo [1 ,4 ]
Capone, Francesca Tari [2 ]
Dabus, Guilherme [1 ,4 ]
Gonzalez-Arias, Sergio [3 ,4 ]
Lau, Patricio E. [4 ]
Samaniego, Edgar A. [1 ]
机构
[1] Baptist Cardiac & Vasc Inst, Dept Intervent Neuroradiol, Miami, FL 33176 USA
[2] Univ Roma La Sapienza, Dept Neurosci & Mental Hlth, Fac Med 2, Rome, Italy
[3] Baptist Hosp Neurosci Ctr, Dept Neurol Surg, Miami, FL USA
[4] Florida Int Univ, Herbert Wertheim Coll Med, Miami, FL 33199 USA
关键词
angiomatosis; Cobb syndrome; embolization; myelopathy; Onyx; spinal angiography; spinal arteriovenous malformation; COBB-SYNDROME; VASCULAR MALFORMATIONS; CUTANEOMENINGOSPINAL ANGIOMATOSIS; EMBOLIZATION; CORD; CLASSIFICATION; HEMANGIOMA; EXPERIENCE; EXCISION; FISTULAS;
D O I
10.3171/2011.12.SPINE11636
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Cutaneomeningospinal angiomatosis, or Cobb syndrome, is a rare metameric developmental disorder presenting as an extradural-intradural vascular malformation that involves bone, muscle, skin, spinal cord, and nerve roots. A 14-year-old girl with a red nevus involving the T6-9 dermatomes on the left side of her back presented with a 5-year history of bowel and bladder incontinence, paraplegia, and lower-extremity sensory loss. Magnetic resonance imaging demonstrated a hemangioma in the T-8 and T-9 vertebral bodies and a spinal cord AVM nidus extending from T-6 to T-9. The AVM was successfully embolized and the patient regained lower-extremity strength, ambulation, and normal sphincter functions after 5 years of having been wheelchair bound. The authors report the restoration of ambulation after endovascular embolization of a large spinal AVM in a patient with long-standing paraplegia due to Cobb syndrome. (http://thejns.org/doi/abs/10.3171/2011.12.SPINE11636)
引用
收藏
页码:408 / 413
页数:6
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