Department of Radiology and Biomedical Imaging, University of California, San Francisco, CA, USA.
AJNR Am J Neuroradiol. 2011 Dec;32(11):E198-200. doi: 10.3174/ajnr.A2413. Epub 2011 Jun 9.
A 7-year-old girl with a history of headaches and Gorham disease was surgically treated in infancy for Chiari I malformation. Subsequent investigation revealed that her cerebellar tonsillar ectopia was due to a long-standing spinal CSF-lymphatic fistula causing intracranial hypotension. Percutaneous fistula closure was performed several times, resulting in transient symptomatic improvement.
一名 7 岁女孩因头痛和 Gorham 病病史,在婴儿期接受了 Chiari I 畸形的手术治疗。随后的检查显示,她的小脑扁桃体异位是由于长期存在的脊髓脑脊液-淋巴瘘导致颅内低血压引起的。多次进行了经皮瘘口闭合术,症状得到了短暂的改善。