Results 31 to 40 of about 12,028 (243)
Aggressive Multiple Central Giant Cell Granulomas of the Jaws
Central giant cell granuloma (CGCG) is considered a benign intraosseous lesion with a varied range of clinical features in two subtypes, including aggressive and non‐aggressive lesions. This study presents a 9‐year‐old boy with multiple bilateral CGCG in the mandible without any systemic disease or specific syndrome.
Farnoush Mohammadi +4 more
wiley +1 more source
An unusual case of polyostotic fibrous dysplasia—A case report
Fibrous dysplasia (FD) is a fibro-osseous lesion where normal bone and marrow is replaced with fibrous tissue, resulting in formation of bone that is weak and prone to expansion.
Kiran Suresh Jagtap +3 more
doaj +1 more source
Epidemiological and Clinical Characteristics of Fibrous Dysplasia of Bone
Objective To describe the epidemiological and clinical characteristics of fibrous dysplasia of bone admitted to a single center in the past 30 years.
XU Hairong +4 more
doaj +1 more source
Surgical correction of valgus deformities of the knee in Polyostotic Fibrous Dysplasia.
Coxa vara and shepherd's crook deformity represent the most common femoral deformities in patients affected by polyostotic fibrous dysplasia (PFD) and McCune Albright syndrome (MAS).
G. Gorgolini +5 more
semanticscholar +1 more source
The explanation of this classification from I to V. Cases presentation for each Type. Objective This study aims to investigate the reliability and clinical outcome of a newly developed classification system for patients with fibrous dysplasia (FD) of the femur and adjacent bones, optimizing its evaluation and management. Methods A total of 205 patients
Yitian Wang +8 more
wiley +1 more source
Fibro-osseous lesion of maxilla. Report of two cases in a family with review of literature [PDF]
Fibrous dysplasia is a disturbance of bone metabolism that is classified as a benign fibro-osseous lesion. Fibrous connective tissue containing abnormal bone, replaces normal bone. The etiology of fibrous dysplasia is unknown.
Kaur, Bhawandeep +2 more
core +1 more source
A case report of McCune–Albright syndrome with hepatic manifestations
Abstract McCune–Albright syndrome is a non‐hereditary disease characterized by café‐au‐lait skin spots, fibrous dysplasia of bone, and endocrinopathies. We report a boy with a history of repeated hospitalizations from birth due to severe jaundice and hyperthyroidism. At the age of 2 years, he suffered from a proximal left femoral fracture.
Mohammad Haddadi +5 more
wiley +1 more source
Polyostotic Fibrous Dysplasia With and Without McCune-Albright Syndrome-Clinical Features in a Nordic Pediatric Cohort [PDF]
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
Clinical, microscopic and imaging findings associated to Mccune-Albright syndrome: report of two cases [PDF]
McCune-Albright syndrome is characterized by the triad café-au-lait cutaneous spots, polyostotic fibrous dysplasia and endocrinopathies. This article presents two cases of McCune-Albright syndrome in a middle-aged woman and a young girl.
BRENTEGANI, Luiz Guilherme +4 more
core +1 more source
Fibrous dysplasia of the spine in a polyostotic form is very rare, with fewer than 36 cases discussed in the literature and there is no such case in Indonesia that has been reported.
Agus Hadian Rahim +3 more
semanticscholar +1 more source

