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[Sturge-Weber syndrome (a report of one case)]
Xi Chen1, Jingrang Li, Jianjun Sun
1Department of Otolaryngology-Head and Neck Surgery, Navy General Hospital, Beijing, 100048, China.
Objective:
To study the etiology, clinical and pathological features, diagnose and treatment of Sturge-Weber syndrome.
Method:
The clinical data of 1 case of Sturge-Weber syndrome was analyzed retrospectively.
Result:
Sturge-Weber syndrome is sporadic neurocutaneous syndrome characterized with facial portwine stains, ocular vascular malformation. DSA can demonstrate excessive blood vessels on the leptomeninges.
Conclusion:
Sturge-Weber syndrome is a rare disease. DSA is helpful for the final diagnosis with its' clinical features.
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