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Juvenile ossifying fibroma: case report and literature review. Management and differential diagnosis

التفاصيل البيبلوغرافية
العنوان: Juvenile ossifying fibroma: case report and literature review. Management and differential diagnosis
المؤلفون: Lemoine Sarah, Cassagnau Elisabeth, Bertin Hélios, Poisson Maria, Corre Pierre, Guiol Julien
المصدر: Journal of Oral Medicine and Oral Surgery, Vol 24, Iss 2, Pp 67-71 (2018)
بيانات النشر: EDP Sciences, 2018.
سنة النشر: 2018
المجموعة: LCC:Dentistry
LCC:Surgery
مصطلحات موضوعية: juvenile ossifying fibroma, fibrous dysplasia, diagnosis, Dentistry, RK1-715, Surgery, RD1-811
الوصف: Introduction: Juvenile ossifying fibroma (JOF) is a rare neoplasm characterized by the replacement of the normal bone matrix with osteo-fibrous tissue. It has the tendency to be locally aggressive despite its benign character and to have a strong tendency for recurrence. Observation: In this case report, the patient is a young man, aged 16, with rapidly advancing maxillary swelling. We describe the diagnostic procedure, the surgical procedure and the differential diagnosis to be eliminated. Discussion: The clinical presentation of JOF, and its rapid growth, can cause fear of other pathologies such as osteosarcoma. The radiological characteristics should reassure the practitioner and a histological examination confirmed the diagnosis. Conclusion: JOF is a benign tumor. It should be operated on at an early stage because of its rapid growth. In its clinical and histological presentation, its trabecular form may mimic an osteosarcoma.
نوع الوثيقة: article
وصف الملف: electronic resource
اللغة: English
تدمد: 2608-1326
Relation: https://www.jomos.org/articles/mbcb/full_html/2018/02/mbcb170043/mbcb170043.html; https://doaj.org/toc/2608-1326
DOI: 10.1051/mbcb/2017023
URL الوصول: https://doaj.org/article/565b82b494694dfebb1b2b3ff2f87d78
رقم الأكسشن: edsdoj.565b82b494694dfebb1b2b3ff2f87d78
قاعدة البيانات: Directory of Open Access Journals
الوصف
تدمد:26081326
DOI:10.1051/mbcb/2017023