SAPHO syndrome with temporomandibular joint ankylosis: clinical, radiological, histopathological, and therapeutical correlations

The SAPHO syndrome is characterized by specific clinical manifestations of synovitis, acne pustulosis, hyperostosis, and osteitis. It is a rare disease with a combination of osseous and articular manifestations associated with skin lesions. We describe a patient with SAPHO syndrome of the mandible a...

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Published inOral surgery, oral medicine, oral pathology, oral radiology and endodontics Vol. 105; no. 3; pp. e67 - e72
Main Authors Utumi, Estevam Rubens, DDS, Oliveira Sales, Marcelo Augusto, DDS, MSc, PhD, Shinohara, Elio Hitoshi, DDS, MSc, PhD, Takahashi, André, DDS, MSc, Coracin, Fábio Luiz, DDS, MSc, Rocha, Rodney Garcia, DDS, MSc, PhD, Paraíso Cavalcanti, Marcelo Gusmão, DDS, MSc, PhD
Format Journal Article
LanguageEnglish
Published United States Mosby, Inc 01.03.2008
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Summary:The SAPHO syndrome is characterized by specific clinical manifestations of synovitis, acne pustulosis, hyperostosis, and osteitis. It is a rare disease with a combination of osseous and articular manifestations associated with skin lesions. We describe a patient with SAPHO syndrome of the mandible and involvement of the temporomandibular joint (TMJ ankylosis). The findings from orthopantomography, computed tomography (CT), and clinical and histopathological examinations are compared and analyzed to improve the final diagnosis. Our patient was submitted to a bilateral high condylectomy and coronoidectomy to correct the open mouth limitation. No previous report of SAPHO syndrome associated with secondary TMJ ankylosis was found in the literature.
Bibliography:ObjectType-Case Study-2
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ISSN:1079-2104
1528-395X
DOI:10.1016/j.tripleo.2007.09.010