Results 81 to 90 of about 4,418 (278)

Polyostotic osteoid osteoma: A case report. [PDF]

open access: yes, 2020
Osteoid osteomas are common, benign osteoblastic tumors that can occur in any bone in the body. They are almost always solitary, with only rare reports of multiple tumors in the same patient.
Bateni, Cyrus   +5 more
core  

A woman with raised alkaline phosphatase and forearm deformity [PDF]

open access: yes, 2011
published_or_final_versio
Chow, WS   +5 more
core   +1 more source

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

open access: yesClinical 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   +8 more
wiley   +1 more source

Effects of zoledronic acid therapy in fibrous dysplasia of bone: a single-center experience

open access: yesArchives of Endocrinology and Metabolism, 2022
Objective: Fibrous dysplasia (FD) is a rare bone disorder that can involve any part of the skeleton, leading to bone pain, deformities, and fractures. Treatment with intravenous bisphosphonates has been used with variable results.
Luciana Pinto Valadares   +6 more
doaj   +1 more source

Sphenoid intraosseous meningioma associated with monostotic hyperostosis “a diagnostic challenge”: case report

open access: yesInternational Journal of Medical and Surgical Sciences
Sphenoidal intraosseous meningioma is included within the extradural brain tumors which constitute less than 2% of the total meningiomas. We describe the case of a 39-year-old female patient who presented with symptoms typical of the location of this ...
J. S. Serna–Trejos   +5 more
semanticscholar   +1 more source

Kyphotic deformity of the lumbar spine due to a monostotic fibrous dysplasia of the second lumbar vertebra: a case report and its surgical management

open access: yesActa Neurochirurgica, 2020
Monostotic fibrous dysplasia (MFD) of the lumbar spine represents an exceedingly rare lesion. A 26-year-old patient presented with a progressive osteolytic lesion of the vertebral body L2 and the diagnosis of MFD.
Anna Stocsits   +5 more
semanticscholar   +1 more source

Polyostotic Fibrous Dysplasia With and Without McCune-Albright Syndrome-Clinical Features in a Nordic Pediatric Cohort [PDF]

open access: yes, 2018
Objective: Fibrous dysplasia (FD) presents as skeletal lesions in which normal bone is replaced by abnormal fibrous tissue due to mosaic GNAS mutation.
Bjornsdottir, Sigridur   +4 more
core   +1 more source

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

open access: yesClinical 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   +3 more
wiley   +1 more source

Characteristics and Treatment Results of 5 Patients with Fibrous Dysplasia and Review of the Literature

open access: yesCase Reports in Endocrinology, 2015
Aim. Fibrous dysplasia is a rare bone disease caused by missense mutation leading to abnormal fibroblast and osteoblast proliferation and increased bone resorption. FD can present in monostotic or polyostotic forms. About 3% of FD could be in association
Nilufer Ozdemir Kutbay   +4 more
doaj   +1 more source

Characterization of an FTLD-PDB family with the coexistence of SQSTM1 mutation and hexanucleotide (G4C2) repeat expansion in C9orf72 gene [PDF]

open access: yes, 2016
The C9orf72 expansion is considered a major genetic cause of familial frontotemporal dementia (FTD) in several patients' cohorts. Interestingly, C9orf72 expansion carriers, present also abundant neuronal p62-positive inclusions.
Almeida, MR   +8 more
core   +1 more source

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