A 10-year review of the occurrence and treatment of central giant cell granulomas, in a District General Hospital

Background:  There is considerable variation in the clinical presentation, behaviour and radiological appearance of central giant cell granulomas (CGCGs), for which multiple treatment modalities have been suggested. Method:  A 10‐year retrospective review of the clinical presentation, radiological f...

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Veröffentlicht in:Journal of oral pathology & medicine 2006-07, Vol.35 (6), p.332-337
Hauptverfasser: Farrier, S. L., Farrier, J. N., Smart, M. K., Nash, E. S.
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container_end_page 337
container_issue 6
container_start_page 332
container_title Journal of oral pathology & medicine
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creator Farrier, S. L.
Farrier, J. N.
Smart, M. K.
Nash, E. S.
description Background:  There is considerable variation in the clinical presentation, behaviour and radiological appearance of central giant cell granulomas (CGCGs), for which multiple treatment modalities have been suggested. Method:  A 10‐year retrospective review of the clinical presentation, radiological features and treatment received was undertaken. Results:  The cohort of patients included six males and three females, with an age range of 7–61 years. Six lesions were in the mandible and three in the maxilla. Eight lesions presented with swelling, three in relation to teeth. One case was an incidental finding. Six cases were confined within the cortical plates, one involved soft tissue. Radiological presentation was diverse, but within the existing confines of CGCGs. With one exception, primary treatment was surgical resection with excisional curettage of the remaining bone; to date, none have recurred. Conclusion:  Diagnosis relies on correct interpretation of clinical, radiographical and histopathological data. Alternative treatments are worthy of consideration, although surgical excision remains the treatment of choice.
doi_str_mv 10.1111/j.1600-0714.2006.00384.x
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One case was an incidental finding. Six cases were confined within the cortical plates, one involved soft tissue. Radiological presentation was diverse, but within the existing confines of CGCGs. With one exception, primary treatment was surgical resection with excisional curettage of the remaining bone; to date, none have recurred. Conclusion:  Diagnosis relies on correct interpretation of clinical, radiographical and histopathological data. 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S.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>A 10-year review of the occurrence and treatment of central giant cell granulomas, in a District General Hospital</atitle><jtitle>Journal of oral pathology &amp; medicine</jtitle><addtitle>J Oral Pathol Med</addtitle><date>2006-07</date><risdate>2006</risdate><volume>35</volume><issue>6</issue><spage>332</spage><epage>337</epage><pages>332-337</pages><issn>0904-2512</issn><eissn>1600-0714</eissn><abstract>Background:  There is considerable variation in the clinical presentation, behaviour and radiological appearance of central giant cell granulomas (CGCGs), for which multiple treatment modalities have been suggested. Method:  A 10‐year retrospective review of the clinical presentation, radiological features and treatment received was undertaken. Results:  The cohort of patients included six males and three females, with an age range of 7–61 years. 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source MEDLINE; Wiley Online Library Journals Frontfile Complete
subjects Adolescent
Adult
calcitonin
Child
corticosteroid
Dentistry
diagnosis
Female
giant cell
granuloma
Granuloma, Giant Cell - diagnostic imaging
Granuloma, Giant Cell - pathology
Granuloma, Giant Cell - surgery
Hospitals, District
Humans
Jaw Diseases - diagnostic imaging
Jaw Diseases - pathology
Jaw Diseases - surgery
Male
Middle Aged
oral
outcome
Radiography
Retrospective Studies
treatment
title A 10-year review of the occurrence and treatment of central giant cell granulomas, in a District General Hospital
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