Results 51 to 60 of about 144,018 (198)

Displasia fibrosa dos ossos da face e do crânio: revisão da literatura e relato de três novos casos. [PDF]

, 1999
Trabalho de Conclusão de Curso - Universidade Federal de Santa Catarina, Centro de Ciências da Saúde, Departamento de Clínica Cirúrgica, Curso de Medicina, Florianópolis ...
Casagrande, Maika Adriana Dione
core  

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

Polyostotic fibrous dysplasia involving the sternum

, 1988
The authors present a case of polyostotic fibrous dysplasia involving the sternum as well.
Marrese, C, PALMIERI, GIAMPIERO, SPAGNOLI, LUIGI GIUSTO, Zorzin, L   +3 more
core   +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

Alveolar bone grafting in association with polyostotic fibrous dysplasia and bisphosphonate-induced abnormal bone turnover in a bilateral cleft lip and palate patient: a case report

, 2012
A case is presented of extensive alveolar bone grafting in a patient with bilateral cleft lip and palate and polyostotic fibrous dysplasia. The patient previously underwent bisphosphonate therapy.
Oguri, Yoshimitsu, Takagi, Ritsuo, Iizuka, Tateyuki, Ogose, Akira, Kodama, Yasumitsu, Ubaidus, Sobhan   +5 more
core   +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

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

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 case of frontal bone aneurysmal bone cyst in association with polyostotic fibrous dysplasia

, 2016
We present the case of a 21 year old male who developed an aneurysmal bone cyst (ABC) on a background of fibrous dysplasia (FD). He was diagnosed with FD aged 4 and has extensive disease with marked craniofacial involvement, including pituitary fossa ...
Duncan, Emma, Hadwen, Thomas
core   +1 more source