نتایج جستجو برای: fibrous dysplasia of bone

تعداد نتایج: 21202898  

1955
Kátia Tôrres Batista Hugo José de Araújo Ulises Prieto y Schwartzman

Fibrous dysplasia is a bone disease characterized by abnormal differentiation of fibrous tissue in the bones; it is often asymptomatic. It may affect one bone (monostotic) or several bones (polyostotic). The monostotic form primarily affects the ribs, but hardly ever affects the hand. It is important to make the differential diagnosis with malignant bone tumors. This article describes the treat...

Journal: :Acta orthopaedica Belgica 2006
Jendrik Hardes Stefanie Scheil-Bertram Georg Gosheger Michael Schulte

In this study, a case of fibromyxoma of the proximal femur in a 59-year old woman is reported. The classification of this rare bone tumour is still a matter of debate and some investigators have suggested that these lesions represent a degenerative form of fibrous dysplasia. Some authors make a further distinction between fibromyxoma and myxoma of bone. In a review of 23 cases of fibromyxoma an...

فتحی, تیمور, فراهینی, حسین ,

Mccune Albright syndrome is a polyosteotic fibrous dysplasia which manifests itself with disturbance of endocrine function and pigmented patch in skin at birth. The prevalence of polyosteotic is between two and three per million. The upper end of femur is the frequent site of involvement in polyosteotic form with multi endocrinopathy and limb deformity and multiple fractures. The presen...

2014
Taha Faruqi Naveen Dhawan Jaya Bahl Vineet Gupta Shivani Vohra Khin Tu Samir M Abdelmagid

A rare disease afflicts less than 200,000 individuals, according to the National Organization for Rare Diseases (NORD) of the United States. Over 6,000 rare disorders affect approximately 1 in 10 Americans. Rare genetic bone disorders remain the major causes of disability in US patients. These rare bone disorders also represent a therapeutic challenge for clinicians, due to lack of understandin...

2013

Fibrous dysplasia (FD) is a benign fibro-osseous bone disease of unknown etiology and uncertain pathogenesis. When bone maturation is completed, indicating the occurence of stabilization is a strong evidence of mechanism. The lesion frequently affects the craniofacial skeleton. The maxilla is affected twice comparing mandible and occurs more frequently in the posterior area. In this case, a 16 ...

2011
Paola Dal Cin

It is characterized by a broad clinical spectrum, varying from the more frequent solitary (monostatic) asymptomatic lesion to extensive and severe multifocal (polyostatic) lesions. The monostotic variant most commonly affects the ribs, femur and tibia of older children and young adults. The less frequent polyostotic type may be associated with endocrine abnormalities, skin hyperpigmentation and...

Journal: :Archives of Otolaryngology–Head & Neck Surgery 2001

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