A CASE REPORT OF STURGE-WEBER SYNDROME WITH PREGNANCY TUMOR

임신성 종양을 동반한 Sturge-Weber Syndrome

  • Rew, Seong-Hun (Dept. of Periodontology, College of Dentistry, Chonbuk National University) ;
  • Kim, Hyung-Seop (Dept. of Periodontology, College of Dentistry, Chonbuk National University)
  • 류성훈 (전북대학교 치과대학 치주과학교실) ;
  • 김형섭 (전북대학교 치과대학 치주과학교실)
  • Published : 1994.07.31

Abstract

We experienced a case of Sturge-Weber Syndrome in a 32 years old female. The diagnosis was established by clinical features of Sturge-Weber Syndrome including unilateral facial portwine nevus, vascular hyperplasia of oral mucosa(espectially 1st & 2nd division of trigeminal nerve). But, plain radiographys of the skull revealed no evidence of calcification. A brief review of related literatures was made. Common Clinical findings in Sturge-Weber Syndrome and specific signs & symptoms manifested by this patient were discussed.

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