POLYOSTOTIC FIBROUS DYSPLASIA

다골성 섬유성 이형성증

  • Lee Kang-Sook (Department of Dental Radiology, College of Dentistry, Kyungpook National University) ;
  • Park Sang-Eok (Department of Dental Radiology, College of Dentistry, Kyungpook National University) ;
  • Choi Karp-Shik (Department of Dental Radiology, College of Dentistry, Kyungpook National University)
  • 이강숙 (경북대학교 치과대학 치과방사선학 교실) ;
  • 박상억 (경북대학교 치과대학 치과방사선학 교실) ;
  • 최갑식 (경북대학교 치과대학 치과방사선학 교실)
  • Published : 1994.06.01

Abstract

Fibrous dysplasia is a benign fibro-osseous condition that is replacement of normal bone and marrow tissues by cellular fibrous tissue and immature bone, and it is divided into monostotic type and polyostotic type. Polyostotic fibrous dysplasia involves multiple bones, such as skull, jaw bones, femur and tibia. And it is also divided into two forms: the less severe Jaffe's type and the more severe Albright's syndrome. Clinically, it frequently occurs in the 2nd decade, and occurs more frequently in maxilla than in mandible. And the lesions of fibrous dysplasia tend to become static as skeletal maturity is reached. The authors experienced three cases of polyostosic fibrous dysplasia in the craniofacial area with the complaints of facial asymmetry due to painless swelling. And we discussed the clinical, radiological, and histopathological features of these cases with a brief review of the literatures.

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