摘要
Sturge-Weber syndrome新生兒通常在出生時臉上有port-wine stain而引起注意。雖然Sturge-Weber syndrome是屬於一種encephalotrigeminal angiomatosis。這些病童出生時的神經學功能往往都是正常的，其後症狀顯現，port-wine stain是病因診斷的依據。現今整型醫學進步，可在嬰兒早期有效地去除port-wine stain，而使診斷失去重要依據。我們報告一個一歲九個月大的男性病人，來到我們的急診時，其臉部皮膚並無明顯病灶，而以重複、過久的非典型熱性痙攣發作來表現。最後才確定診斷為Sturge-Weber syndrome，目前抗癲癇藥物有效的控制其痙攣的發作。
並列摘要
Sturge-Weber syndrome were diagnosed based on the presence of facial port-wine stains noted since birth. This case came to our ER with the chief complaint of a seizure attack accompanied by fever and vomiting. The initial impression was febrile convulsion. However, his repeated, prolonged seizure alerted us. After a thorough assessment of history and further examination, we confirmed that the case was Sturge-Weber syndrome. With the advancement of modern cosmetic medicine, the characteristic port-wine stain could be eliminated easily in early infancy, which could make this kind of case a challenge to first-line physicians when facing a patient with unexplained prolonged and repetitive seizures.
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