Klippel-Trenaunay-Weber Syndrome (KTWS) and Spontaneous Spinal CSF Leak: Coincidence or Link

被引:0
作者
Mokri, Bahram [1 ]
机构
[1] Mayo Clin, Dept Neurol, Rochester, MN 55905 USA
来源
HEADACHE | 2014年 / 54卷 / 04期
关键词
cerebrospinal fluid leak; Klippel-Trenaunay-Weber syndrome; angiogenesis; limb asymmetry; connective tissue matrix; ANGIOGENESIS; DISORDER;
D O I
10.1111/head.12262
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
ObjectiveTo highlight the occurrence of spontaneous cerebrospinal fluid (CSF) leak in the setting of Klippel-Trenaunay-Weber syndrome (KTWS). BackgroundKTWS is a congenital multicomponent disorder of angiogenesis plus limb asymmetry. The cause of spontaneous CSF leaks often remains unknown, but the notion of a pre-existing dural weakness related to a disorder of connective tissue matrix is gaining momentum. Report of Cases and MethodsTwo women with KTWS developed spontaneous CSF leaks. Each underwent extensive head and spine imaging studies. One patient underwent surgery to treat the CSF leak and later an epidural blood patch upon partial recurrence of her symptoms. The other patient, who had intermittent CSF leak, developed cerebral venous thrombosis requiring several months of anticoagulation therapy. Both patients have histories of visceral bleeding: gastrointestinal in 1 patient and genitourinary in the other. ResultsThe predominant site of vascular anomaly was the left lower limb in 1 patient and the right upper limb in the other, while the involved limb was larger in 1 patient and smaller in the other. Each patient presented with orthostatic headaches. One had additional choreiform movements and cognitive difficulties that responded to the treatment of the leak. Head magnetic resonance imaging in both patients showed diffuse pachymeningeal enhancement and evidence of sinking of the brain. Computed tomography myelography in 1 patient disclosed the site of the leak; and she underwent surgery to treat the leak, and later an epidural blood patch upon partial recurrence of her symptoms to which she responded well. The other patient had intermittent leak with history of long remission and was reluctant to go through invasive diagnostic or therapeutic measures. ConclusionThe occurrence of an uncommon disorder (spontaneous CSF leak) in the setting of a rare congenital disorder in 2 unrelated patients is intriguing. Whether this represents coincidence or a link is not clear but deserves further observations and investigation.
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页码:726 / 731
页数:6
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