Results 71 to 80 of about 3,294 (221)
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 +8 more
wiley +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 +7 more
wiley +1 more source
Monostotic fibrous dysplasia of the spine: report of a case involving a cervical vertebra [PDF]
, 2018 Monostotic fibrous dysplasia of the spine is a rare entity. Only 26 cases, of which 11 were located in the cervical spine, are to be found in the literature.
Heini, P. +3 more
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Mc Cune Albright syndrome: gynecological perspective [PDF]
, 2023 The key features of McCune-Albright syndrome include sexual precocious puberty, polyostotic fibrous dysplasia and café au lait spots. It is associated with hyperfunction of multiple endocrine glands.
Dharani E. +2 more
core +2 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 +3 more
wiley +1 more source
A case of polyostotic fibrous dysplasia
Journal of the Korean Radiological Society, 1972 Chul‐Kee Park, KW Seo
openalex +3 more sources
The nature of fibrous dysplasia [PDF]
, 2009 Fibrous dysplasia has been regarded as a developmental skeletal disorder characterized by replacement of normal bone with benign cellular fibrous connective tissue.
A Corsi +24 more
core +3 more sources
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 +5 more
wiley +1 more source
Neuropathic-like pain in fibrous dysplasia/McCune-Albright syndrome [PDF]
, 2022 Context: Pain is a major symptom in adults with fibrous dysplasia/McCune-Albright syndrome (FD/MAS) and response to current treatments, including bisphosphonates and standard analgesics (nonsteroidal anti-inflammatory drugs and opiates) is unpredictable.
Boyce, Alison M +6 more
core +2 more sources
Pathological fracture in fibrous dysplasia: a case report [PDF]
, 2022 Fibrous dysplasia (FD) is described as a growth disorder characterized by the progressive replacement of normal bone elements by fibrous-osseus tissue. Bones affected by FD is presented with bone weakening and prone to pathological fracture.
Supriyadi, Bambang
core +2 more sources