Results 231 to 240 of about 32,206 (267)
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Fibrous dysplasia of the spine
Clinical Radiology, 1988Fibrous dysplasia affecting the spine is unusual. A further 11 cases are reported and the radiological features are described. The complications and difficulties with the diagnosis of this condition are discussed.
J F, Wright, D J, Stoker
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An aggressive fibrous dysplasia
Oral Surgery, Oral Medicine, Oral Pathology, 1974Abstract A case of aggressive fibrous dysplasia is presented. The lesion progressed rapidly after the initial investigative biopsy and became quiescent only after three successive surgical shaves. Pathologic specimens continually supported the diagnosis of monostotic fibrous dysplasia.
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Fibrous dysplasia of the mandible
The American Journal of Surgery, 1955Abstract Four cases of fibrodysplastic lesions of the mandible have been presented. Their histologic structure is essentially the same but their clinical picture and behavior differ widely. At present, out of many conflicting opinions, the concept of fibrous dysplasia as a benign tumor originating in a mesenchymal defect seems to be the most ...
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Craniofacial Fibrous Dysplasia
Oral and Maxillofacial Surgery Clinics of North America, 2012Despite recent advances in the understanding of the natural history and molecular abnormalities, many questions remain surrounding the progression and management of fibrous dysplasia (FD). In the absence of comorbidities, the expected behavior of craniofacial FD (CFD) is to be slow growing and without functional consequence.
Pat, Ricalde +2 more
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The British Journal of Radiology, 1971
The radiological features of 55 histologically confirmed and fully documented cases of fibrous dysplasia have been reviewed, together with a brief review of the method of presentation. There were 46 cases of monostotic fibrous dysplasia and nine polyostotic cases. The features of the two groups have been assessed separately, then compared.
M J, Gibson, J H, Middlemiss
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The radiological features of 55 histologically confirmed and fully documented cases of fibrous dysplasia have been reviewed, together with a brief review of the method of presentation. There were 46 cases of monostotic fibrous dysplasia and nine polyostotic cases. The features of the two groups have been assessed separately, then compared.
M J, Gibson, J H, Middlemiss
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The Journal of Pediatrics, 1949
Summary A case of polyostotic fibrous dysplasia in a 5-year-old girl is reported. The diagnosis was made by the characteristic triad of predominantly unilateral bone lesions, precocious “puberty,” and unilateral skin pigmentation, and was substantiated by radiographic and pathologic examination of the bone lesions. The early onset of menses (second
L J, HACKETT, W M, CHRISTOPHERSON
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Summary A case of polyostotic fibrous dysplasia in a 5-year-old girl is reported. The diagnosis was made by the characteristic triad of predominantly unilateral bone lesions, precocious “puberty,” and unilateral skin pigmentation, and was substantiated by radiographic and pathologic examination of the bone lesions. The early onset of menses (second
L J, HACKETT, W M, CHRISTOPHERSON
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Clinical Nuclear Medicine, 1984
Fibrous dysplasia, a bone dysplasia of unknown pathogenesis, may be either monostotic or polyostotic. Not only is the femur involved in nearly all cases of the polyostotic form, but a distinct unilateral predilection is often noted. The following case illustrates the classic polyostotic changes.
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Fibrous dysplasia, a bone dysplasia of unknown pathogenesis, may be either monostotic or polyostotic. Not only is the femur involved in nearly all cases of the polyostotic form, but a distinct unilateral predilection is often noted. The following case illustrates the classic polyostotic changes.
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Fibrous Dysplasia in Craniosynostosis
Journal of Craniofacial SurgeryPurpose: This case series presents 2 pediatric patients diagnosed with craniosynostosis who subsequently developed fibrous dysplasia. The aim is to describe their clinical presentation, management, and outcomes.
Lauren Middleton +2 more
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Fibrous Dysplasia of the Skull
Journal of Neurosurgery, 1951W, FEIRING, E H, FEIRING, L M, DAVIDOFF
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