• Title/Summary/Keyword: Pindborg 종양

Search Result 2, Processing Time 0.02 seconds

The Calcifying Epithelial Odontogenic Tumor: Report of a Case (석회화 상피성 치성종양의 증례보고)

  • Lee Seung-Hyun;Hwang Eui-Hwan;Lee Sang-Rae;Hosaka Mitsuo
    • Journal of Korean Academy of Oral and Maxillofacial Radiology
    • /
    • v.28 no.2
    • /
    • pp.521-537
    • /
    • 1998
  • The calcifying epithelial odontogenic tumor is a rare benign odontogenic neoplasm which was first described by Pindborg in 1955 and accounts for less than 1% of all odontogenic tumors. The tumor occurs primarily in the molar-premolar region of the mandible, and 52% of cases are associated with an unerupted tooth. The clinical feature is most commonly a slow-growing painless swelling. The tumor may show considerable radiographic variation and usually characteristic histopathologic features. In this study, we report a case of the calcifying epithelial odontogenic tumor on the left mandibular body and ramus area in a 28-year-old male with a brief review of the concerned literatures.

  • PDF

Calcifying epithelial odontogenic tumor (CEOT) in palate: report of a case (구개에 발생한 석회화 상피성 치성 종양: 증례보고)

  • Kim, Joong-Min;Jang, Hyon-Seok;Rim, Jae-Suk;Jun, Sang-Ho;Park, Jung-Kyun;Ju, Hyun-Joong;Lee, Eui-Seok
    • Journal of the Korean Association of Oral and Maxillofacial Surgeons
    • /
    • v.37 no.1
    • /
    • pp.77-80
    • /
    • 2011
  • A calcifying epithelial odontogenic tumor (CEOT) was first described as a separate entity in 1955 by Pindborg, and has since been referred to as Pindborg tumor. CEOT is characterized by the presence of squamous-cell proliferation, calcification and amyloid deposits, and accounts for only 1% of all odontogenic tumors. CEOT is a benign, though occasional locally invasive, slow-growing neoplasm. It is located either intraosseously or extraosseously, and is usually associated with an unerupted permanent tooth. A 24 year-old female visited our clinic, presenting with a palatal swelling and intra-oral ulcer. After an incisional biopsy, the lesion was confirmed to be odontogenic tumor. A tumor resection and reconstruction surgery with tongue flap were performed.