Results 121 to 130 of about 11,759 (256)

An unusual presentation of non-specific cystic degeneration of craniofacial fibrous dysplasia: a case report and review of literature

open access: yesMaxillofacial Plastic and Reconstructive Surgery, 2020
Background Fibrous dysplasia (FD) is a rare, sporadic, and benign congenital condition in which normal cancellous bone is replaced by fibro-osseous tissue with immature osteogenesis.
Inseok Hong   +4 more
doaj   +1 more source

Surgical treatment of craniofacial fibrous dysplasia in adults [PDF]

open access: yes, 2014
pre-printCraniofacial fibrous dysplasia is a rare disorder that may require neurosurgical expertise for definitive management; however, surgical management of FD in adult patients is uncommon. Although other therapies have been shown to slow progression,
Bowers, Christian A.   +1 more
core  

First two cases of craniomaxillofacial fibrous dysplasia from Nepal – case series

open access: yesClinical, Cosmetic and Investigational Dentistry, 2018
Neha Mishra,1 Sourav Kumar Rout2 1Department of Oral and Maxillofacial Pathology and Microbiology, Chitwan Medical College and Teaching Hospital, Bharatpur-10, Chitwan, Nepal; 2Department of Oral and Maxillofacial Surgery, Chitwan Medical College and ...
Mishra N, Rout SK
doaj  

Fibrous dysplasia of Faciomaxillary region case reports and review of literature [PDF]

open access: yes, 2012
This article discusses the author's experience in managing fibrous dysplasia of faciomaxillary region. Data was accumulated from 2005 – 2011. All these cases were managed by the author.Commonest bone involved by fibrous dysplasia was maxilla (Literature ...
Thiagarajan, Balasubramanian
core   +1 more source

Polyostotic Fibrous Dysplasia Mimicking Metastatic Disease Radiographically: A Case Report and Literature Review [PDF]

open access: yes, 2017
Fibrous dysplasia is a benign intramedullary lesion characterized by an excessive proliferation of cellular fibrous tissue intermixed with irregular trabeculae. It involves any of the bones presenting as monostotic, polyostotic, or panostotic lesion.
Ahmed, MD, Shahida   +4 more
core   +1 more source

Atualização em etiologia, diagnóstico e manejo da precocidade sexual [PDF]

open access: yes, 2008
Precocious puberty is defined as the development of secondary sexual characteristics before the age of 8 years in girls and 9 years in boys. Gonadotropin-dependent precocious puberty (GDPP) results from the premature activation of the hypothalamic ...
ARNHOLD, Ivo J. P.   +3 more
core   +2 more sources

Quadruple osteotomy: A simple approach to treat “O” deformity in hypophosphatemic rickets

open access: yesJournal of Orthopedics, Traumatology and Rehabilitation, 2018
Multiple deformities of femur and tibia in a child are known to occur in various conditions such as multiple hereditary exostosis, polyostotic fibrous dysplasia, Osteogenesis imperfecta, achondroplasia, multiple epiphyseal dysplasia, and rickets.
Alok Chandra Agarwal   +4 more
doaj   +1 more source

Pathophysiology and medical treatment of pain in fibrous dysplasia of bone [PDF]

open access: yes, 2012
One of the most common complications of fibrous dysplasia of bone (FD) is bone pain. Usual pain killers are often of inadequate efficacy to control this bone pain.
Chapurlat, Roland D   +5 more
core   +4 more sources

Fibrous dysplasia polyostotic. Apropos of a patient

open access: yesActa Médica del Centro, 2017
Fibrous dysplasia is a benign fibro-osseous condition consisting of the substitution of bone tissue for fibrous tissue; it is considered a benign pseudotumoral lesion of the skeleton and it is usually asymptomatic.
Madyaret Águila Carbelo   +2 more
doaj  

Leontiasis ossea and post traumatic cervical cord contusion in polyostotic fibrous dysplasia [PDF]

open access: yes, 2006
Leontiasis ossea (leonine facies) or cervical canal stenosis are rare complications of polyostotic fibrous dysplasia (PFD). This case report documents dramatic leontiasis ossea in PFD as well as post traumatic cervical cord contusion due to ...
AI Leet   +11 more
core   +3 more sources

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