Oral fibrolipoma: A rare histological variant
نویسندگان
چکیده
منابع مشابه
Oral Fibrolipoma-A Rare Histological Entity: Report of 3 Cases and Review of Literature
Lipomas are rare benign soft tissue mesenchymal neoplasms in the oral cavity, representing 1% of all benign oral tumors. Fibrolipoma (FL), an uncommon, histological variant of the classic lipoma, mostly affects the buccal mucosa. Very few cases of FL have been reported in the English literature. To the best of our knowledge a review of the English literature showed 33 cases of FL affecting the ...
متن کاملoral fibrolipoma-a rare histological entity: report of 3 cases and review of literature
lipomas are rare benign soft tissue mesenchymal neoplasms in the oral cavity, representing 1% of all benign oral tumors. fibrolipoma (fl), an uncommon, histological variant of the classic lipoma, mostly affects the buccal mucosa. very few cases of fl have been reported in the english literature. to the best of our knowledge a review of the english literature showed 33 cases of fl affecting the ...
متن کاملOral Fibrolipoma of Oral Cavity
Fibrolipoma, a benign tumor, is classified as a variant of conventional lipoma. It usually presents as a soft, smoothsurfaced nodular masses that can be sessile or pedunculated. Most of them are less than 3 cm in size, but it can become much larger. The buccal mucosa and buccal vestibule are the most common intraoral sites. Here, we present a new case of this uncommon oral lipofibroma that pres...
متن کاملReviewing the Entity: Retropharyngeal Fibrolipoma and a Rare Case Report
Introduction: Fibrolipoma, a subtype of lipoma is painless, well-circumscribed, slow-growing, submucosal benign adipocyte tumour. It is uncommon in the oral cavity and oropharyngeal region, with rare incidence in the retropharynx even rarest in pediatric age group. Case Report: A very unusual case of fibrolipoma is presented in a pediatric patient, who had a huge retropharyngeal fibrolipoma a...
متن کاملHolt-Oram Syndrome: A Rare Variant
Holt-Oram syndrome is an autosomal dominant disorder, characterised by skeletal abnormalities of the upper limb associated with congenital heart defect, mainly atrial and ventricular septal defects. Skeletal defects exclusively affect the upper limbs in the preaxial radial ray distribution and are bilateral and asymmetrical. They range from clinodactyly, absent or digitalised thumb, hypoplastic...
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: Indian Journal of Dental Research
سال: 2014
ISSN: 0970-9290
DOI: 10.4103/0970-9290.147123