Format

Send to

Choose Destination
Br J Oral Maxillofac Surg. 2007 Oct;45(7):567-70. Epub 2006 Oct 6.

Cherubism: long-term follow-up of 2 patients in whom it regressed without treatment.

Author information

1
Department of Oral Surgery and Pathology, School of Dentistry, Universidade Federal de Minas Gerais, Belo Horizonte, Brazil. guilhermeccs@ufmg.br

Abstract

Cherubism is a rare hereditary, self-limiting fibrous dysplasia characterised by painless enlargement of the jaws in childhood. Although, it is accepted that the lesions of cherubism are eventually replaced by bone, there have been few long-term follow-up reports with clinicoradiographic documentation of spontaneous remission of the disease, without treatment. We report two cases of cherubic boys who were followed for 17 and 19 years. Clinicoradiographic examination during this period showed regression of the disease without surgical correction.

PMID:
17030358
DOI:
10.1016/j.bjoms.2006.08.013
[Indexed for MEDLINE]

Supplemental Content

Full text links

Icon for Elsevier Science
Loading ...
Support Center