Results 41 to 50 of about 1,135 (176)

Monostotic fibrous dysplasia of the temporal bone

The Journal of Laryngology & Otology, 1999
AbstractFibrous dysplasia is a slowly progressive bony disorder where normal bone is replaced by abnormal fibroosseous tissue. Its monostotic variety in the temporal bone is very rare and such a case is presented here. Computed tomography (CT) may be adequate for the diagnosis and follow-up of these patients.
Xenellis, J, Bibas, A, Savy, L, Maragoudakis, P, Nomicos, P   +4 more
openaire   +3 more sources

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

A Rare Cause of Shoulder Pain: Monostotic Fibrous Dysplasia

The Turkish Journal of Gastroenterology, 2016
Fibrous dysplasia is a rare bone disease which has a wide spectrum of symptoms depending on the involvement area such as pain, deformity, fracture, dyspnea or visual loss. One of the rare involvement areas is the bones around the shoulder.
Bayram KELLE, Aygül POLAT KELLE, Kıvılcım EREN ERDOĞAN, Erkan KOZANOĞLU   +3 more
doaj  

Fibrous Dysplasia versus Juvenile Ossifying Fibroma: A Dilemma

Case Reports in Dentistry, 2016
Fibrous dysplasia (FD) is a condition characterized by excessive proliferation of bone forming mesenchymal cells which can affect one bone (monostotic type) or multiple bones (polyostotic type). It is predominantly noticed in adolescents and young adults.
Sreelakshmi N. Nair, Raghavendra Kini, Prasanna Kumar Rao, Gowri P. Bhandarkar, Roopashri Rajesh Kashyp, Manjunath Rai, Neel Naik, Athul Santhosh   +7 more
doaj   +1 more source

Mazabraud's syndrome: A case report supported by molecular studies and review of the literature

Bone Reports, 2023
Mazabraud's syndrome represents rare benign disorder characterized by simultaneous occurrence of fibrous dysplasia of bone and intramuscular myxomas within surrounding soft tissue.
Ludvík Kašpar, Jan Balko, Martina Strnadová, Lenka Krsková, David Máška, Josef Zámečník   +5 more
doaj   +1 more source

Radiologic Aspects of Segmental Odontomaxillary Dysplasia: A Case Report

Case Reports in Dentistry, Volume 2025, Issue 1, 2025.
Segmental odontomaxillary dysplasia (SOD) is a rare nonheritable unilateral developmental disorder characterized by dental, bone, and soft tissue abnormalities. A 13‐year‐old female patient presented with mild facial asymmetry. Clinical examination revealed right maxillary enlargement and gingival overgrowth.
Alessandra Landim, Regina Garcia Dorta, Andresa Borges Soares, Carolina de Paula Rossetto Lisboa, Fabrício Passador-Santos, Alexandre Luís Filócomo, José Luiz Cintra Junqueira, Mariana Quirino Silveira Soares, Hannah Wesley   +8 more
wiley   +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

Locally aggressive monostotic fibrous dysplasia of the cervical spine mimicking malignancy: a case report and literature review

SICOT-J, 2019
We report the case of a 30-year-old woman with histologically proven monostotic fibrous dysplasia of C2 revealed by a pathological fracture of the odontoid process. Radiological investigations showed a ground-glass mineralization of the vertebral body, a
Milon Audrey, Polivka Marc, Larousserie Fréderique, Lot Guillaume, Ziza Jean-Marc, Laredo Jean-Denis   +5 more
doaj   +1 more source

Monostotic Fibrous Dysplasia Involving the Mandible: A Case Report

SAGE Open Medical Case Reports, 2020
Fibrous dysplasia (FD) is a skeletal developmental anomaly, which is non-hereditary and idiopathic in origin. It is characterized by the replacement of normal bone with the excess proliferation of fibrous tissue in irregular bony trabeculae.
Khalil Ibrahim Assiri
doaj   +1 more source