Results 41 to 50 of about 1,632 (147)

Melorheostosis: Clinical, radiological, and histopathological features with a literature review

Physiological Reports, Volume 13, Issue 21, November 2025.
Abstract Melorheostosis is a rare sclerosing bone dysplasia that can clinically and radiologically mimic common bone disorders, particularly in atypical presentations. Its heterogeneous manifestations and limited awareness among clinicians frequently contribute to diagnostic delays or misdiagnosis. We report the case of a 34‐year‐old woman with chronic
Elif Koca, Şeyhmus Kavak, Bilal Demir, Nil Comunoglu, Fatih Kantarci, Oguzhan Koca   +5 more
wiley   +1 more source

An Unusual Complication After Surgical Correction of Shepherd's Crook Deformity in a Young Woman: A Case Report and Literature Review

Medicine Advances, Volume 3, Issue 3, Page 193-196, September 2025.
An 18‐year‐old female patient presented with shepherd's crook deformity in the left lower limb and was subsequently diagnosed with MAS according to the genetic analysis. This patient developed acute heart failure in the second morning after proximal femur osteotomy without preoperative cardiovascular abnormality or excessive liquid supplementation in ...
Rongjie Wu, Guangtao Fu
wiley   +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

Prophylactic intramedullary nailing of the proximal femur in a case of McCune Albright syndrome – A case report & review of literature

Journal of Orthopaedic Reports, 2023
Introduction: Premature puberty, café-au-lait pigmentation, polyostotic fibrous dysplasia, and/or varied endocrine disorders make up the unusual condition known as McCune Albright Syndrome.
Mrinal Mahadev Kambli, Shaswat Mishra, Sagar Bansal, Sachin Khemkar, Sanjeev Ghildiyal, Manish Jain   +5 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

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

Fibrous Dysplasia: Clinicopathologic Presentation of 36 Cases

Türk Patoloji Dergisi, 2018
Objective: Fibrous dysplasia is a slowly progressing bone lesion resulting from displacement of the normal medullary bone with abnormal fibroosseous tissue.
Mine ÖZŞEN, Ülviye YALÇINKAYA, Muhammed Sadık BILGEN, Zeynep YAZICI   +3 more
doaj   +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

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