منابع مشابه
Non-familial cherubism--a case report.
A case of cherubism in a 9 year old boy with no familial history is presented. Clinical features, histologic appearance, radiographic findings, differential diagnosis and rationale for treatment is discussed.
متن کاملCherubism: 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 1 Introduction
Cherubism, a very rare disorder with only an estimated 300 cases reported in the literature, is a benign hereditary condition of the mandible and/or maxilla, usually found in children between 2 and 5 years of age giving characteristic cherubic appearance to the patient. On radiography, the lesions exhibit bilateral multilocular radiolucent areas. Histopathology reveals multinucleated giant cell...
متن کاملOrbital involvement in cherubism.
PURPOSE To demonstrate the clinical, radiologic, and histopathologic features of a patient with orbital involvement in cherubism that prompted surgical treatment. DESIGN Single interventional case report. INTERVENTION Findings of the ophthalmic evaluation, computed tomography (CT) scans, intraoperative examination, and light microscopy of the specimens were analyzed. MAIN OUTCOME MEASURES...
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ژورنال
عنوان ژورنال: Journal of Oral and Maxillofacial Pathology
سال: 2014
ISSN: 0973-029X
DOI: 10.4103/0973-029x.131920