نتایج جستجو برای: ossifying
تعداد نتایج: 1270 فیلتر نتایج به سال:
We present a case of a 40-year-old man with secondary fibrosarcoma of bone, arising from a non-ossifying fibroma. He subsequently developed metastatic disease that responded to four successive chemotherapy courses, the last three using the same dose/schedule of single agent ifosfamide. Eventual rapid progression of a huge intra-abdominal mass was associated with the syndrome of extrapancreatic ...
Introduction: Non-ossifying Fibroma (NOF) is a relatively common benign and non-neoplastic lesion in long bones of children and adolescents. As far as very few cases of NOF have been reported in jaws and what was managed to be found regarding all reported cases having occurred only in the mandible, in this article we are going to report a case of maxillary NOF in a 38-year-old female.
Introduction: To report two unusual cases of primary hyperparathyroidism (HPT) that initially manifested with a “ jaw tumor” and to discuss the clinical implications of a giant cell granuloma vs an ossifying fibroma of the jaw. Material and methods: The history, physical examination, laboratory values and the imaging and pathologic findings are described in two patients who presented with a “ja...
Fibro-osseous lesions of the maxillofacial bones should be classified based on their radiographic growth pattern. This method can simplify this category of lesions, which have considerable overlapping histologic features. These neoplasms can be grouped into three categories: (a) fibrous dysplasia; (b) ossifying fibroma; (c) and osseous dysplasia. Important lesions in the differential diagnosis ...
Hyperparathyroidism-jaw tumour syndrome detected by aggressive generalized osteitis fibrosa cystica.
Severe hyperparathyroidism can affect bone metabolism and be in the origine of multiple brown tumours (generalized osteitis fibrosa cystica). When associated with fibro-ossifying tumours of the jaw, it realizes a rare genetic syndrome referred as Hyperparathyroidism-jaw tumour HPT-JT. We report the case of a patient we treated for HPT-JT, and literature review.
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