Results 61 to 70 of about 144,018 (198)

Fibrous dysplasia of Faciomaxillary region case reports and review of literature [PDF]

, 2012
This article discusses the author's experience in managing fibrous dysplasia of faciomaxillary region. Data was accumulated from 2005 – 2011. All these cases were managed by the author.Commonest bone involved by fibrous dysplasia was maxilla (Literature ...
Thiagarajan, Balasubramanian; Stanley Medical college
core  

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

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

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

MALIGNANT CHANGE IN FIBROUS DYSPLASIA

, 1964
A brief review of the literature on malignant change occurring in fibrous dysplasia is given and a further case of a sarcoma arising in a patient with polyostotic fibrous dysplasia is reported.
D. M. Riddell
core   +1 more source

RANK‐L inhibitor as a promising agent for refractory extensive craniofacial fibrous dysplasia: A case report

Head &Neck, Volume 46, Issue 1, Page E1-E5, January 2024.
Abstract Background McCune‐Albright syndrome is a rare disorder characterized by polyostotic fibrous dysplasia (FD), café‐au‐lait skin pigmentation, and endocrine dysfunction. Extensive FD in the craniofacial region can present significant challenges in terms of disease control and carries a high risk of permanent visual impairment.
Moataz D. Abouammo, Mohammad Bilal Alsavaf, Daniel M. Prevedello, Luma Ghalib, Alison M. Boyce, Ricardo L. Carrau   +5 more
wiley   +1 more source

Polyostotic fibrous dysplasia associated with intramuscular myxomas: Mazabraud syndrome

, 2015
The authors report a new case of Mazabraud syndrome in a 69-year-old woman complaining of pain in her right thigh. Plain radiographs demonstrated radiological findings consistent with polyostotic fibrous dysplasia of the right femur and tibia.
Luis Ramos Pascua, Teresa Lorenzo Dominguez, Jose Daniel Samper Wamba, Maria Jose Fernandez Bermudez   +3 more
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Familial gigantiform cementoma with recurrent ANO5 p.Cys356Tyr mutations: Clinicopathological and genetic study with literature review

Molecular Genetics &Genomic Medicine, Volume 12, Issue 1, January 2024.
This study revealed three patients with familial gigantiform cementoma (FGC) carried the heterozygous mutation c.1067G>A (p.Cys356Tyr) in the ANO5 gene which was not found in 8 juvenile ossifying fibromas, 5 polyostotic fibrous dysplasia and 5 florid cemento‐osseous dysplasia.
Zheng Zhou, Ye Zhang, Lijing Zhu, Yajuan Cui, Yan Gao, Chuan‐Xiang Zhou   +5 more
wiley   +1 more source

POLYOSTOTIC FIBROUS DYSPLASIA—ALBRIGHT'S SYNDROME

, 1949
1. Four cases of polyostotic fibrous dysplasia are presented. 2. All are males, all show cutaneous pigmentation, and in two there has been precocious puberty. 3.
C. K. Warrick
core   +1 more source

Polyostotic fibrous dysplasia of the mandible and bony nasal septum with intracranial expansion [PDF]

, 2016
Fibrous dysplasia is an uncommon benign tumour in the nasal cavity. Due to adjacent vital soft tissue structures surgery is often the treatment of choice.
Rautiainen, Markus, Numminen, Jura
core   +1 more source