Results 21 to 30 of about 13,284 (234)

Navigation-guided nasal endoscopic surgery for acute vision loss caused by fibrous dysplasia: a case report and review of literatures

open access: yesBMC Surgery, 2022
Background Bone fibrous dysplasia is a benign disease of bone tissue dysplasia. Vision impairment is the commonest neurological complication of craniofacial fibrous dysplasia.
Weijie Liu   +7 more
doaj   +1 more source

Malignant transformation of monostotic fibrous dysplasia into angiosarcoma in the proximal tibia

open access: yesIndian Journal of Pathology and Microbiology, 2021
The majority of bone angiosarcomas are primary tumors while secondary angiosarcomas arise after radiation therapy or bone infarctus. This article presents a case of malignant transformation of monostotic fibrous dysplasia into angiosarcoma.
Selin Narter   +3 more
doaj   +1 more source

Sphenoid Bone Dysplasia: A Rare Cause of Compressive Optic Neuropathy Mimicking Glaucoma [PDF]

open access: yes, 2023
Fibrous dysplasia is a benign, rare bone disease in which bone is replaced by fibro-osseous tissue to varying degrees. It can present differently depending on the amount of compression caused by the fibro-osseous tissue. Patients are usually asymptomatic,
Pelin Kıyat   +7 more
core   +1 more source

Monostotic fibrous dysplasia in a 10-year-old patient

open access: yesBLDE University Journal of Health Sciences, 2021
Fibrous dysplasia is a rare congenital bone disorder which manifests as a localized defect in osteoblastic differentiation and maturation with the replacement of normal bone with an abnormal scar-like fibrous connective tissue.
Gayatri Nayanar, Mamatha G S. Reddy
doaj   +1 more source

Secondary aneurysmal bone cyst of the frontal bone with fibrous dysplasia showing rapid expansion: a case report [PDF]

open access: yes, 2023
A 19-year-old woman presented with swelling of the left forehead without pain. She did not have any relevant past or family history. Computed tomography showed destruction of the outer cortex of the frontal bone.
Kuwabara, Kyoko   +8 more
core   +1 more source

Nonvascular autologous fibular cortical strut graft with internal fixation in monostotic fibrous dysplasia of femur neck- A case report

open access: yesJournal of Orthopaedic Reports, 2022
Introduction: Fibrous dysplasia is a non-inheritable congenital disorder characterized by bone-forming expansile fibrous lesions that disrupt normal bone architecture.
Mitali Mokashi   +3 more
doaj   +1 more source

Nonspecific cystic degeneration in craniofacial fibrous dysplasia: A rare finding

open access: yesContemporary Clinical Dentistry, 2022
Fibrous dysplasia (FD) is a developmental pathology of the bones in which normal bone is replaced by fibrous tissue and immature bone. It can affect single bone (monostotic) or multiple bones (polyostotic), sporadically or in association with McCune ...
Vindhya Savithri   +3 more
doaj   +1 more source

Polyostotic fibrous dysplasia: imaging findings of a controversial case [PDF]

open access: yesDigital Diagnostics, 2022
Fibrous dysplasia is a rare non-neoplastic tumor-like congenital bone disease that is most likely associated with GNAS gene mutations, with a broad spectrum of clinical presentations, ranging from isolated monostotic and polyostotic forms to other extra ...
Francesca De Michele   +3 more
doaj   +1 more source

Craniofacial Fibrous Dysplasia in an Elderly Patient: A Case Report with a Review of Literature

open access: yesActa Stomatologica Croatica, 2015
Fibrous dysplasia is a benign fibro-osseous disorder, characterized by fibrous connective tissue containing abnormal bone which replaces normal bone. It represents 2 to 5% of all bone tumors and 7% of all benign tumors.
Suresh K. Sachdeva
doaj   +1 more source

Best practice management guidelines for fibrous dysplasia/McCune-Albright syndrome: a consensus statement from the FD/MAS international consortium

open access: yesOrphanet Journal of Rare Diseases, 2019
Fibrous Dysplasia / McCune Albright syndrome (FD/MAS) represents a wide spectrum of diseases due to somatic gain-of-function mutations of the GNAS gene. The mutation leads to overactivity in the target tissues and to a wide phenotype of clinical features
Muhammad Kassim Javaid   +20 more
doaj   +1 more source

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