Results 71 to 80 of about 2,787 (193)
Head &Neck, Volume 46, Issue 1, Page E1-E5, January 2024.Abstract Background McCune‐Albright syndrome is a rare disorder characterized by polyostotic fibrous dysplasia (FD), café‐au‐lait skin pigmentation, and endocrine dysfunction. Extensive FD in the craniofacial region can present significant challenges in terms of disease control and carries a high risk of permanent visual impairment.
Moataz D. Abouammo +5 more
wiley +1 more source
Molecular Genetics &Genomic Medicine, Volume 12, Issue 1, January 2024.This study revealed three patients with familial gigantiform cementoma (FGC) carried the heterozygous mutation c.1067G>A (p.Cys356Tyr) in the ANO5 gene which was not found in 8 juvenile ossifying fibromas, 5 polyostotic fibrous dysplasia and 5 florid cemento‐osseous dysplasia.
Zheng Zhou +5 more
wiley +1 more source
Síndrome de Mazabraud: Presentación de un caso clínico y revisión de la literatura [PDF]
, 2000 El síndrome de Mazabraud se define como la asociación de una tumoración de partes blandas, el mixoma intramuscular, y un tumor óseo, la displasia fibrosa.
Maqueda Abreu, V. +4 more
core
Fibrous Dysplasia versus Juvenile Ossifying Fibroma: A Dilemma
Case Reports in Dentistry, 2016 Fibrous dysplasia (FD) is a condition characterized by excessive proliferation of bone forming mesenchymal cells which can affect one bone (monostotic type) or multiple bones (polyostotic type). It is predominantly noticed in adolescents and young adults.
Sreelakshmi N. Nair +7 more
doaj +1 more source
Monostotic Fibrous Dysplasia Involving the Mandible: A Case Report
SAGE Open Medical Case Reports, 2020 Fibrous dysplasia (FD) is a skeletal developmental anomaly, which is non-hereditary and idiopathic in origin. It is characterized by the replacement of normal bone with the excess proliferation of fibrous tissue in irregular bony trabeculae.
Khalil Ibrahim Assiri
doaj +1 more source
A Case of Atypical McCune-Albright Syndrome with Vaginal Bleeding [PDF]
, 2011 Background: McCune-Albright syndrome (MAS) is a rare non-inherited disorder characterized by the clinical triad of precocious puberty, cafe-au-lait skin lesions, and fibrous dysplasia of bone.
Hashemipour, M. +4 more
core +1 more source
PET-positive fibrous dysplasia - a potentially misleading incidental finding in a patient with intimal sarcoma of the pulmonary artery [PDF]
, 2018 Benign bone tumors can show an increased FDG uptake in FDG-PET/CT investigations. In the presented case, an incidentally detected PET-positive asymptomatic fibrous dysplasia was initially misinterpreted as a metastasis in a patient with intimal sarcoma ...
Bode, Beata +3 more
core
CT Imaging of Craniofacial Fibrous Dysplasia
Case Reports in Dentistry, 2015 Fibrous dysplasia is a benign fibroosseous bone dysplasia that can involve single (monostotic) or multiple (polyostotic) bones. Monostotic form is more frequent in the jaws. It is termed as craniofacial fibrous dysplasia, when it involves, though rarely,
Zerrin Unal Erzurumlu +3 more
doaj +1 more source
Fibrous dysplasia of bone causing unilateral proptosis
Medical Journal of Dr. D.Y. Patil University, 2015 Fibrous dysplasia (FD) is a slow growing benign noninherited disorder in which normal bones are replaced by fibrous tissue and immature woven bones. Here we report a case of 30-year-old female who presented with unilateral proptosis and lagophthalmos ...
Reshma Ramakrishnan +3 more
doaj +1 more source