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Dentigerous Cyst and Ameloblastoma of the Jaws.
Barrett, Andrew W; Sneddon, Kenneth J; Tighe, John V; Gulati, Aakshay; Newman, Laurence; Collyer, Jeremy; Norris, Paul M; Coombes, Darryl M; Shelley, Michael J; Bisase, Brian S; Liebmann, Rachael D.
Affiliation
  • Barrett AW; 1 Queen Victoria Hospital NHSF Trust, East Grinstead, West Sussex, UK.
  • Sneddon KJ; 1 Queen Victoria Hospital NHSF Trust, East Grinstead, West Sussex, UK.
  • Tighe JV; 1 Queen Victoria Hospital NHSF Trust, East Grinstead, West Sussex, UK.
  • Gulati A; 1 Queen Victoria Hospital NHSF Trust, East Grinstead, West Sussex, UK.
  • Newman L; 1 Queen Victoria Hospital NHSF Trust, East Grinstead, West Sussex, UK.
  • Collyer J; 1 Queen Victoria Hospital NHSF Trust, East Grinstead, West Sussex, UK.
  • Norris PM; 1 Queen Victoria Hospital NHSF Trust, East Grinstead, West Sussex, UK.
  • Coombes DM; 1 Queen Victoria Hospital NHSF Trust, East Grinstead, West Sussex, UK.
  • Shelley MJ; 1 Queen Victoria Hospital NHSF Trust, East Grinstead, West Sussex, UK.
  • Bisase BS; 1 Queen Victoria Hospital NHSF Trust, East Grinstead, West Sussex, UK.
  • Liebmann RD; 1 Queen Victoria Hospital NHSF Trust, East Grinstead, West Sussex, UK.
Int J Surg Pathol ; 25(2): 141-147, 2017 Apr.
Article de En | MEDLINE | ID: mdl-27621276
ABSTRACT

AIM:

To determine how many ameloblastomas were misdiagnosed as dentigerous cysts (DCs) by correlating the radiological and histopathological features of a series of both entities. METHODS AND

RESULTS:

Histopathology reports and radiological imaging of 135 DCs and 43 ameloblastomas were reviewed. Any clinical or radiological feature that suggested that the diagnosis of DC was wrong-for example, absence of an unerupted tooth-prompted review of the original histology. A total of 34 cases coded as DC at diagnosis were excluded; in the remaining 101 patients, the clinicoradiological and histopathological features were consistent with DC in 96 (95.0%). Review of the histology revealed that 4 patients had actually had odontogenic keratocysts (OKCs) and one a luminal/simple unicystic ameloblastoma (UA). One other OKC and 3 other ameloblastomas (1 luminal UA, 2 solid/multicystic) had originally been diagnosed as DC; these had been identified prior to the study. Of the 9 misdiagnosed patients, 6 were ≤20 years old. Clinically, DC had been the only, or one of the differential, diagnoses in 7 patients; in the other 2, the clinical diagnosis was radicular cyst. In none of the 4 misdiagnosed ameloblastomas was the radiology compatible with a diagnosis of DC. Incorrect terminology had been used on the histopathology request form in 5 of the 34 excluded cases where the clinical diagnosis was DC, despite the cyst being periapical to an erupted carious or root-filled tooth.

CONCLUSIONS:

The entire clinical team must ensure that a histopathological diagnosis of DC is consistent with the clinicoradiological scenario, particularly in younger patients.
Sujet(s)
Mots clés

Texte intégral: 1 Collection: 01-internacional Base de données: MEDLINE Sujet principal: Améloblastome / Kyste dentigère / Tumeurs de la mâchoire / Erreurs de diagnostic Type d'étude: Clinical_trials / Diagnostic_studies / Prognostic_studies Limites: Adolescent / Adult / Child / Female / Humans / Male / Middle aged Langue: En Journal: Int J Surg Pathol Sujet du journal: PATOLOGIA Année: 2017 Type de document: Article Pays d'affiliation: Royaume-Uni

Texte intégral: 1 Collection: 01-internacional Base de données: MEDLINE Sujet principal: Améloblastome / Kyste dentigère / Tumeurs de la mâchoire / Erreurs de diagnostic Type d'étude: Clinical_trials / Diagnostic_studies / Prognostic_studies Limites: Adolescent / Adult / Child / Female / Humans / Male / Middle aged Langue: En Journal: Int J Surg Pathol Sujet du journal: PATOLOGIA Année: 2017 Type de document: Article Pays d'affiliation: Royaume-Uni