Craniofacial fibrous dysplasia with aneurysmal bone cyst: A rare coexistence
نویسندگان
چکیده
Fibrous dysplasia (FD) is a developmental anomaly in which the normal bone marrow replaced by fibro-osseous tissue. can affect either single (monostotic) or multiple (polyostotic) bones. Craniofacial FD monostotic involving craniofacial However, CFD one of rare forms FD. Aneurysmal cyst (ABC) non-neoplastic lesion. ABCs are expansile lytic lesions composed numerous blood-filled channels and cystic spaces that mostly involve long bones vertebrae occur rarely as primary bony lesion secondary to various pre-existing benign malignant tumors like fibrous dysplasia. Concomitant occurrence ABC with only few cases reported literature. Here, we report on case 24-year-old woman who had presented right frontal facial swelling for over 6 years followed proptosis eye. Computed tomography revealed an peripheral ground glass densities body greater wing sphenoid, lateral wall orbit, squamous part temporal associated thinning rarefaction walls. Further, MRI same patient some them showing fluid-fluid levels within.
منابع مشابه
Craniofacial Fibrous Dysplasia
Fibrous dysplasia (FD) is an osseous growth dis-order, producing immature bone and characte-rized by the replacement of normal bone with fibro-osseous connective tissue. It is a bone dys-plasia that has the potential to cause significant cosmetic and functional disturbances, particularly in the craniofacial skeleton. Cra-niofacial fibrous dysplasia is one of the three types of polyostotic fibro...
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Fibrous dysplasia is a benign bone disease first described by Lichtenstein in 1938. It is characterized by progressive replacement of normal bone with fibro-osseous connective tissue. When the disease involves craniofacial skeleton, it results in significant disfigurement and other functional problems. This paper reports a case of large craniofacial fibrous dysplasia involving zygomaticomaxilla...
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ژورنال
عنوان ژورنال: International journal of radiology and diagnostic imaging
سال: 2022
ISSN: ['2664-4436', '2664-4444']
DOI: https://doi.org/10.33545/26644436.2022.v5.i3a.273