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J Oral Maxillofac Surg ; 77(6): 1278.e1-1278.e7, 2019 Jun.
Article in English | MEDLINE | ID: mdl-30880133

ABSTRACT

Cherubism is an autosomal-dominant inherited mutation in the SH3BP2 gene on chromosome 4p16.3. It is characterized by bilateral symmetric fibro-osseous lesions that are limited to the maxilla and mandible. The lesions present in early childhood and typically spontaneously involute after puberty. Current standard practice is to reserve surgery for symptomatic or severely disfiguring cases. This report presents 3 patients with cherubism who exhibited marked reduction in tumor size with imatinib, a tyrosine kinase inhibitor. Treatment was well tolerated, with few side effects.


Subject(s)
Antineoplastic Agents , Cherubism , Imatinib Mesylate , Tooth , Adaptor Proteins, Signal Transducing/genetics , Antineoplastic Agents/therapeutic use , Cherubism/drug therapy , Child , Child, Preschool , Humans , Imatinib Mesylate/therapeutic use , Mandible , Maxilla
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