Results 71 to 80 of about 12,028 (243)
Prevention of pathological fracture in fibrous dysplasia of proximal femur in a 24-year-old female a rare presentation - a case report [PDF]
Fibrous dysplasia (FD) was historically mentioned in the medical literature in 1938 by Dr. Lichtenstein and in 1942 by Dr. Lichtenstein and Jaffe. The term Jaffe-Lichtenstein syndrome is sometimes used synonymously with monostotic FD or to denote cases ...
Mhatre, Jayesh, Modi, Nihar, Supe, Amit
core +2 more sources
Osteoid Osteoma of the Occipital Condyle in Adolescents: Surgical Resection Under Navigation
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
Polyostotic Fibrous Dysplasia: A Case Report
Polyostotic fibrous dysplasia (PFD) is a scarce noncancerous bone condition characterized by the failure to form mature lamellar bone and arrest in the form of woven bone, resulting in deformities and functional limitations. Extreme forms of craniofacial
Arun Aram +3 more
semanticscholar +1 more source
Post‐COVID‐19 Exacerbation of a Stable Fibrous Dysplasia: A Case Report
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
Treatment of Peripheral Precocious Puberty [PDF]
There are many etiologies of peripheral precocious puberty (PPP) with diverse manifestations resulting from exposure to androgens, estrogens, or both. The clinical presentation depends on the underlying process and may be acute or gradual.
Eugster, Erica A., Schoelwer, Melissa
core +1 more source
Polyostotic fibrous dysplasia: a clinical case
Fibrous dysplasia is a benign pathological process with various manifestations. Sometimes the volume of lesions leads to «malignant» course of disease. This article presents a clinical case of a patient with a rare disabling isolated polyostotic form of ...
E. Kharitonova +2 more
semanticscholar +1 more source
Skeletal Phenotype in Mulibrey Nanism, A Monogenic Skeletal Dysplasia With Fibrous Dysplasia
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
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 +5 more
doaj +1 more source
Misdiagnosis of a Paediatric Fibrous Dysplasia of the Mandible. [PDF]
Fibrous dysplasia (FD) is a chronic benign bone lesion, mainly affecting young individuals, that could be monostotic or polyostotic in nature leading to the replacement of normal bone with the excess proliferation of fibrous tissue.
Alawadhi R, Alsairefi S, AlMutairi MM.
europepmc +2 more sources
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

