Clinical, radiographic, and histological findings of florid cemento-osseous dysplasia: a case report
Identifieur interne : 004267 ( Main/Curation ); précédent : 004266; suivant : 004268Clinical, radiographic, and histological findings of florid cemento-osseous dysplasia: a case report
Auteurs : Jeong-Hee Kim [Corée du Sud] ; Byeong-Chul Song [Corée du Sud] ; Sun-Ho Kim [Corée du Sud] ; Yang-Soon Park [Corée du Sud]Source :
- Imaging Science in Dentistry [ 2233-7822 ] ; 2011.
Abstract
Cemento-osseous dysplasias are a group of disorders known to originate from periodontal ligament tissue and involve, essentially, the same pathological process. They are usually classified into three main groups: periapical, florid, and focal cemental dysplasias depending on their extent and radiographic appearances. Radiographically, florid cementoosseous dysplasia (FCOD) appears as dense, lobulated masses, often symmetrically located in various regions of the jaws. The best management for the asymptomatic FCOD patient consists of regular recall examinations with prophylaxis. The management of the symptomatic patient is more difficult. A case of FCOD occurring in a 52-year-old edentulous Korean female is reported which is rare with regard to race and sex.
Url:
DOI: 10.5624/isd.2011.41.3.139
PubMed: 22010072
PubMed Central: 3189539
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<front><div type="abstract" xml:lang="en"><p>Cemento-osseous dysplasias are a group of disorders known to originate from periodontal ligament tissue and involve, essentially, the same pathological process. They are usually classified into three main groups: periapical, florid, and focal cemental dysplasias depending on their extent and radiographic appearances. Radiographically, florid cementoosseous dysplasia (FCOD) appears as dense, lobulated masses, often symmetrically located in various regions of the jaws. The best management for the asymptomatic FCOD patient consists of regular recall examinations with prophylaxis. The management of the symptomatic patient is more difficult. A case of FCOD occurring in a 52-year-old edentulous Korean female is reported which is rare with regard to race and sex.</p>
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