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CASE REPORT
Cherubism with multiple dental abnormalities: a rare presentation
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  1. Satya Ranjan Misra1,
  2. Lora Mishra2,
  3. Neeta Mohanty3,
  4. Susant Mohanty4
  1. 1Department of Oral Medicine and Radiology, Institute of Dental Sciences, Bhubaneswar, Odisha, India
  2. 2Department of Conservative Dentistry and Endodontics, Institute of Dental Sciences, Bhubaneswar, Odisha, India
  3. 3Department of Oral Pathology and Microbiology, Institute of Dental Sciences, Bhubaneswar, Odisha, India
  4. 4Department of Paediatric Dentistry, Institute of Dental Sciences, Bhubaneswar, Odisha, India
  1. Correspondence to Professor Neeta Mohanty, drneeta2014{at}gmail.com

Summary

Cherubism is a progressive, hereditary fibro-osseous lesion exclusively affecting the jaw bones. It is caused by the abnormal functioning of osteoblasts and osteoclasts, leading to replacement of normal bone by cellular fibrous tissue and immature bone, which produces painless progressive growth of the jaw, with a round facial appearance. It was first described in 1933 by Jones as ‘familial multilocular cystic disease of the jaws’. The term ‘cherubism’ was later coined to describe the rounded facial appearance resulting from jaw hypertrophy that was reminiscent of cherubs depicted throughout Renaissance art. The bony lesions generally occur at an early age, affect one or both jaws symmetrically, and grow progressively until puberty. Spontaneous regression is seen in most cases, although surgical re-contouring may be required for others for aesthetic reasons.

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