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Pyogenic granuloma mimicking peripheral dentinogenic ghost‐cell tumour recurrence: case report and meta‐analytic literature update

Identifieur interne : 002948 ( Main/Exploration ); précédent : 002947; suivant : 002949

Pyogenic granuloma mimicking peripheral dentinogenic ghost‐cell tumour recurrence: case report and meta‐analytic literature update

Auteurs : B. Pommer [Autriche] ; G. Dvorak [Autriche] ; K. Rappersberger [Autriche] ; R. C. K. Jordan [États-Unis] ; G. Watzek [Autriche] ; M. A. Pogrel [États-Unis]

Source :

Oral Surgery [ 1752-2471 ] ; 2013-05.

RBID : ISTEX:E364C4931F20A384AF611D769081550F69E85FAF

Descripteurs français

Wicri :
- topic : Unité périphérique.

English descriptors

Abstract

Peripheral (extraosseous) dentinogenic ghost‐cell tumours are extremely rare neoplasms, representing less than 1% of all odontogenic tumours. Only 28 cases (including the present report) are described in literature: the majority of patients (89%) are over 40 years of age (mean: 59.1 ± 20.5 years) and 63% are male. Seventy‐three per cent are located in the mandible, and anterior jaw regions are most commonly affected (74%). Erosion of the underlying bone can be observed in 53% radiographically. The present case report describes a recurrent swelling after excisional biopsy of a peripheral dentinogenic ghost‐cell tumour in the anterior maxilla of a 78‐year‐old male patient mimicking tumour recurrence. Histopathological examination of the second biopsy, however, revealed no evidence of ghost‐cell tumour recurrence but development of a pyogenic granuloma. In contrast to central dentinogenic ghost‐cell tumours, there is no evidence of recurrence of peripheral dentinogenic ghost‐cell tumours in literature to date.

Url:

https://api.istex.fr/document/E364C4931F20A384AF611D769081550F69E85FAF/fulltext/pdf

DOI: 10.1111/ors.12019

Affiliations:

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Le document en format XML

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<front><div type="abstract">Peripheral (extraosseous) dentinogenic ghost‐cell tumours are extremely rare neoplasms, representing less than 1% of all odontogenic tumours. Only 28 cases (including the present report) are described in literature: the majority of patients (89%) are over 40 years of age (mean: 59.1 ± 20.5 years) and 63% are male. Seventy‐three per cent are located in the mandible, and anterior jaw regions are most commonly affected (74%). Erosion of the underlying bone can be observed in 53% radiographically. The present case report describes a recurrent swelling after excisional biopsy of a peripheral dentinogenic ghost‐cell tumour in the anterior maxilla of a 78‐year‐old male patient mimicking tumour recurrence. Histopathological examination of the second biopsy, however, revealed no evidence of ghost‐cell tumour recurrence but development of a pyogenic granuloma. In contrast to central dentinogenic ghost‐cell tumours, there is no evidence of recurrence of peripheral dentinogenic ghost‐cell tumours in literature to date.</div>
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Pyogenic granuloma mimicking peripheral dentinogenic ghost‐cell tumour recurrence: case report and meta‐analytic literature update

Pyogenic granuloma mimicking peripheral dentinogenic ghost‐cell tumour recurrence: case report and meta‐analytic literature update

Source :

Descripteurs français

English descriptors

Abstract

Links toward previous steps (curation, corpus...)

Le document en format XML

Pour manipuler ce document sous Unix (Dilib)

Pour mettre un lien sur cette page dans le réseau Wicri