Results 111 to 120 of about 11,759 (256)

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, Peruze Celenk, Emel Bulut, Yakup Sancar Barıs   +3 more
doaj   +1 more source

Fibrous dysplasia of maxilla: Report of two cases

Journal of Indian Academy of Oral Medicine and Radiology, 2015
Fibrous dysplasia (FD) is an idiopathic skeletal disorder in which the trabecular bone is replaced and distorted by poorly organized, structurally unsound fibro-osseous tissue. The lesion is classified into two forms: Monostotic (75-80%) and polyostotic.
Nisha Dua, Neetu Singla, Saloni Arora, Shaveta Garg   +3 more
doaj   +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., Martín López, P., Miralles Muñoz, F. A., Sanz Reig, J., Sebastiá Forcada, Emilio   +4 more
core  

Diagnosis and management of benign fibro-osseous lesions of the jaws: a current review for the dental clinician [PDF]

, 2016
Benign fibro-osseous lesions of the maxillofacial skeleton constitute a heterogeneous group of disorders that includes developmental, reactive (dysplastic) and neoplastic lesions. Although their classification has been reviewed multiple times in the past,
Kauzman, Adel, Mainville, Gisèle, Turgeon, D.P.   +2 more
core   +1 more source

Spinal polyostotic fibrous dysplasia in two adults: Does only biopsy unravel the mystery?

Indian Journal of Endocrinology and Metabolism, 2013
Polyostotic fibrous dysplasia is a rare non-inheritable genetic disease due to mutation in GNAS gene. Here we present two adults who were accidentally detected lytic lesions in spine and after extensive evaluation for malignancies; was diagnosed on ...
Abhay Gundgurthi, M K Garg, Reena Bhardwaj, Sandeep Kharb, Aditi Pandit, Karninder S Brar, Ravi Kumar, A G Pandit   +7 more
doaj   +1 more source

Incidence and Prevalence of Fibrous Dysplasia/McCune-Albright Syndrome: A Nationwide Registry-Based Study in Denmark

Journal of Clinical Endocrinology and Metabolism
Context Fibrous dysplasia/McCune-Albright syndrome (FD/MAS) is a rare genetic disorder. Incidence and prevalence are not well-studied. Epidemiological research is complicated by the rarity of FD/MAS, absence of registries, heterogeneous presentation, and
M. Meier, Emese Vágó, Bo Abrahamsen, O. Dekkers, E. Horváth-Puhó, L. Rejnmark, Natasha M. Appelman-Dijkstra   +6 more
semanticscholar   +1 more source

Radiological conference. Enchondroma [PDF]

, 1998
published_or_final_versio
Peh, WCG, Wong, LLS
core  

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, Saurabh Shrivastava, Anamika Patel, Anjaneya Agashe   +3 more
doaj   +1 more source

MR and CT findings of cyst degeneration of sphenoid bone in McCune-Albright syndrome: a case report [PDF]

, 2009
© 2009 Li et al; licensee BioMed Central Ltd.
A Ahmed, A Al Kaissi, A McLaughlin, CE Dumitrescu, Dan Wang, DJ McCune, E Diah, F Albright, JS Lee, M Riminucci, MC Papadopoulos, N Bulakbaşı, Ping Li, S Lumbroso, Xian-Feng Li, Xu-Dong Xia, Ying Jiang, Zai-Ren Zhang   +17 more
core   +3 more sources

A Case of Craniofacial Polyostotic Fibrous Dysplasia

Journal of Radiology Case Reports, 2010
We present the case of a patient with craniofacial polyostotic fibrous dysplasia. Polyostotic fibrous dysplasia is relatively rare and usually presents in late childhood/early adulthood. It is occasionally associated with endocrine disorders such as McCune-Albright syndrome.
William Keith Carson, Justin Clark
openaire   +3 more sources