Central Giant Cell Granuloma in a Child: Case Report
نویسندگان
چکیده
منابع مشابه
Multifocal Central Giant Cell Granuloma - A Case Report
Central giant cell granuloma is a benign, aggressive neoplasm composed of multinucleated giant cells that almost exclusively occurs in the jaws though extra-gnathic incidence is rare.Multifocal CGCGs of the jaws are very rare and suggestive of systemic diseases such as hyperparathyroidism,an inherited syndrome such as Noonan-like multiple giant cell lesion syndrome or other disorders.Very few c...
متن کاملCentral giant cell granuloma. A case report.
Central giant cell granuloma (CGCG) is a relatively uncommon benign bony lesion of a variably aggressive nature. Thought to represent a reparative response to intrabony haemorrhage and inflammation, CGCG was once regarded as a reactive lesion. It is actually an asymptomatic lesion which becomes evident during routine radiographic examination or as a result of painless but visible expansion of t...
متن کاملMultiple Central Giant Cell Granuloma of the Mandible: A Case Report
Introduction: Central giant cell granuloma is a benign lesion but sometimes has aggressive proliferation composed of multinucleated giant cells in a background of spindle and ovoid mesenchymal cells. Multifocal central giant cell granuloma of jaws is very rare and usually associated with hyperparathyroidism and some syndromes. We described an un-usual case of a 22-year-old man with idi-opathic ...
متن کاملGiant cell granuloma in a child: case report.
This article describes a case of central giant cell granuloma in the right posterior region of mandible in a 10-year-old girl. The lesion was removed by curettage and a histopathological examination was carried out. Clinical and radiographic follow-up showed total removal of the lesion. The importance of early diagnosis of this type of lesion is emphasized, mainly in children.
متن کاملTumor-induced rickets in a child with a central giant cell granuloma: a case report.
Tumor-induced osteomalacia/rickets is a rare paraneoplastic disorder associated with a tumor-producing fibroblast growth factor 23 (FGF23). We present a child with symptoms of rickets as the first clinical sign of a central giant cell granuloma (CGCG) with high serum levels of FGF23, a hormone associated with decreased phosphate resorption. A 3-year-old boy presented with a limp and 6 months la...
متن کاملذخیره در منابع من
با ذخیره ی این منبع در منابع من، دسترسی به آن را برای استفاده های بعدی آسان تر کنید
ژورنال
عنوان ژورنال: International journal of odontostomatology
سال: 2016
ISSN: 0718-381X
DOI: 10.4067/s0718-381x2016000300004