Results 61 to 70 of about 2,105 (203)

The “Phantom of the Opera” sign of craniofacial fibrous dysplasia with unilateral polyostotic involvement in McCune-Albright syndrome [PDF]

, 2017
McCune-Albright syndrome is a very rare genetic disorder resulting from a sporadically occurring somatic \textit{GNAS} gene mutation. It is characterised by the association of: endocrinopathy (most commonly precocious puberty), polyostotic fibrous ...
W. Phillip Law, Peter Jackson
core   +1 more source

Osteoid Osteoma of the Occipital Condyle in Adolescents: Surgical Resection Under Navigation

Clinical Case Reports, Volume 13, Issue 5, May 2025.
ABSTRACT This article reports a 12‐year‐old male with occipital condyle osteoid osteoma, presenting with neck pain and limited motion, unresponsive to conservative treatment. CT revealed a right condylar lesion. Surgical excision via a right paramedian suboccipital incision achieved complete recovery, confirmed by pathology and 3‐month follow‐up.
Yiji Li, Mingquan Liu, Dongao Zhang, Yinqian Wang, Xingang Zhao, Kun Wu, Zijun Zhao, Ze Ding, Tao Fan   +8 more
wiley   +1 more source

Post‐COVID‐19 Exacerbation of a Stable Fibrous Dysplasia: A Case Report

Clinical Case Reports, Volume 13, Issue 4, April 2025.
ABSTRACT Fibrous dysplasia (FD) is a rare, benign fibro‐osseous lesion characterized by replacement of normal bone with extensive fibrous stroma due to abnormalities in osteoblast differentiation. After puberty and during adulthood, FD lesions usually become quiescent. However, some cases show signs of regrowth and reactivation.
Mohammed Taib Fatih, Mohammed Abdalla Mahmood, Mohammed Khalid Mahmood, Amanj Ismael Tahir, Handren Ameer Kurda, Mohammed Aso Abdulghafor, Balen Hamid Qadir, Zana Fuad Noori   +7 more
wiley   +1 more source

Jaffe Lichtenstein Type of Polyostotic Skeletal Fibrous Dysplasia With the Involvement of Cranial Bones [PDF]

, 2021
Fibrous dysplasia (FD), a benign fibro-osseous bone tumor commonly involving the craniofacial region, presents a wide spectrum of radiographic patterns.
Ozlem Akkemik, Onder Kalenderer, Kalenderer, Onder, Akkemik, Ozlem, Dundar, Nesrin, Serkan Erkus, Erkus, Serkan, Nesrin Dündar   +7 more
core   +1 more source

Imaging of Fibrous Dysplasia: A Comprehensive In-Depth Analysis of Monostotic, Polyostotic, Syndromic Forms, and Bone Sarcoma Development

Journal of Imaging
Fibrous dysplasia is one of the most common skeletal lesions. The wide spectrum of clinical manifestations ranges from asymptomatic conditions (typical of monostotic forms) to severe skeletal diseases with deformity and fractures for polyostotic fibrous ...
Paolo Spinnato, Nicola Marrone, Domenico Romeo, Matilde Gonçalves, Roberts Naglis, Leonardo Di Battista, Elena Pedrini, Maria Parisi, Raffaella Rinaldi, Silvia Gazzotti, Alberto Righi, Marco Colangeli   +11 more
doaj   +1 more source

Skeletal Phenotype in Mulibrey Nanism, A Monogenic Skeletal Dysplasia With Fibrous Dysplasia

Clinical Genetics, Volume 107, Issue 3, Page 271-277, March 2025.
We present a cross‐sectional detailed radiographic evaluation of the skeletal phenotype in 33 patients, aged 4.5–48 years, with Mulibrey nanism (MUL). This study confirms MUL as a skeletal dysplasia with prenatal‐onset growth failure, slender bones, vertebral changes, and a high prevalence of fibrous dysplasia and fractures.
Susann Karlberg, Sanna Toiviainen‐Salo, Marita Lipsanen‐Nyman, Outi Mäkitie   +3 more
wiley   +1 more source

Two-stage surgical treatment of complex femoral deformities with severe coxa vara in polyostotic fibrous dysplasia [PDF]

, 2015
In patients with polyostotic fibrous dysplasia with extensive femoral involvement, severe coxa vara may cause complex femoral deformities that are difficult to treat with a single-stage surgical procedure.
FARSETTI, PASQUALE, IPPOLITO, ERNESTO, POTENZA, VITO, Farsetti, P, Valentini, MB, Potenza, V, Ippolito, E   +6 more
core   +1 more source

Rebound Hypercalcemia After Denosumab Cessation in Adult Fibrous Dysplasia: A Case Report and Clinical Alert

Case Reports in Endocrinology, Volume 2025, Issue 1, 2025.
Background: Fibrous dysplasia (FD) is a rare congenital bone disease. Denosumab, a monoclonal antibody targeting nuclear factor kappa‐B ligand (RANKL), suppresses osteoclast activity and exhibits therapeutic potential for FD. Case Presentation: We present the case of an adult female patient diagnosed with FD who had undergone 7 treatment cycles of ...
Danni Liu, Jiayi Chen, Hongmei Chen, Wenxue Hu, Jinxin Lin, Kalyani Sen   +5 more
wiley   +1 more source

Late‐Onset Nonhereditary Cherubism: First Reported Case in Ghana With Review of Diagnostic and Management Challenges

Case Reports in Radiology, Volume 2025, Issue 1, 2025.
Background Cherubism is a rare genetic disorder characterised by multilocular cystic lesions in the mandible and/or maxilla, which result in the typical cherub‐like face. Two forms of cherubism exist—hereditary (familial) and nonhereditary (nonfamilial)—and it usually occurs amongst children aged 2–7 years.
Seth Kwadjo Angmorterh, Mariella Mawunyo Amoussou-Gohoungo, Adam Inusah, Bridgette Palm, Kafui Kossi Kekessie, Riaan van de Venter, Sonia Aboagye, Cosmos Yarfi, John Nsor-Atindana, Portia Mamle Angmorterh, Klenam Dzefi-Tettey, Anusha Vaddi   +11 more
wiley   +1 more source

Recovery of neurological deficit after posterior total en-bloc resection of locally aggressive polyostotic fibrous dysplasia

Journal of Orthopaedic Reports
Summary of background data: A case report of polyostotic and locally aggressive fibrous dysplasia including thoracic spine and rib with the symptom of neurologic deficit. In adulthood Polyostotic fibrous dysplasia which occurs in mature bone and behavior
Abdullah Iyigun, Omer Polat, Bekir Yavuz Ucar, Necdet Saglam   +3 more
doaj   +1 more source