A case of cherubism with spondyloarthropathy
نویسندگان
چکیده
منابع مشابه
Cherubism: A Case Report
Cherubism, a pediatric disease, is a self limiting non-neoplastic autosomal dominant fibro-osseous disorder of jaws. It is a self limiting disease and rarely apparent before the age of two years. It occurs in children and predominantly in boys. It is characterized by clinical bilateral swelling of cheeks due to bony enlargement of jaws that give the patient a typical 'cherubic' look. Regression...
متن کاملCherubism--a case report.
Introduction: Cherubism is a rare, non neoplastic, fibroosseous disorder seen in children which is characterized by bilateral painless enlargement of the jaws giving a cherubic appearance to the patient. It is an autosomal dominant disorder but may occur sporadically as well. The treatment of cherubism is contentious. It is said that the disease regresses by itself and even after regression, ...
متن کاملCherubism: A Variant Case
Introduction: Cherubism, a form of osteolytic genetic disorder presents in childhood and tends to regress spontaneously after puberty. It is characterized by painless expansion of mandible or maxilla or both. Case Report: On radiography, the lesions exhibit bilateral multinuclear radiolucent areas. Histopathology reveals multinucleated giant cells in the background of proliferating fibrous conn...
متن کاملCherubism. A case report.
Cherubism is a rare disorder with autosomal dominant inheritance. It is classified as a benign fibro-osseous lesions and may involve either facial bone. Its typical dentofacial deformities are caused by mutations in the SH3BP2 gene. The protein encoded by SH3BP2 had a significant role in the regulation of osteoblasts and osteoclasts. Accordingly with the radiological findings, differential diag...
متن کاملCherubism: a case report.
Cherubism is a familial benign fibro-osseous disease of the jaws. On radiography, the lesions exhibit bilateral multinuclear radiolucent areas. Histopathology reveals multinucleated giant cells in the background of proliferating fibrous connective tissue. Mutations in the SH3BP2 gene are identified as the cause of cherubism. A 12-year-old girl with prominence of the lower face was investigated....
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ژورنال
عنوان ژورنال: International Journal of Rheumatic Diseases
سال: 2015
ISSN: 1756-1841
DOI: 10.1111/1756-185x.12597