作者: Mohammad ShakeelMohammad ImranMunaza ShafMudasar Ahad
刊名: Oral and Maxillofacial Pathology Journal, 2015, Vol.6 (1), pp.578-581
来源数据库: Kairali Society of Oral & Maxillofacial Pathologists
DOI: 10.5005/jp-journals-10037-1041
关键词: Autosomal DominantCherubismGiant CellsFibrousdysplasia.
原始语种摘要: ABSTRACTCherubism, a very rare disorder with only an estimated 300 cases reported in the literature, is a benign hereditary condition of the mandible and/or maxilla, usually found in children between 2 and 5 years of age giving characteristic cherubic appearance to the patient. On radiography, the lesions exhibit bilateral multilocular radiolucent areas. Histopathology reveals multinucleated giant cells in the background of proliferating fibrous connective tissue. The present case report describes cherubism in a 10 years old male child and briefy reviews literature on this report.How to cite this article: Shakeel M, Imran M , Shaf M , Ahad M. Cherubism. Oral Maxillofac Pathol J 2015;6(1):578-581.
全文获取路径: 凯拉莉口腔及颌面部病理学家学会 

  • cherubism 家族性颌骨增大
  • mandible 下颌
  • multilocular 多室的
  • literature 文献
  • hereditary 遗传性
  • radiolucent 透媚
  • bilateral 双边的
  • maxilla 上颌骨
  • connective 连索
  • child 小孩