Results 251 to 260 of about 26,036 (310)
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The Journal of Bone & Joint Surgery, 1951
Experience with nine cases indicates that fibrous dysplasia of bone may present a variable clinical picture. In adults there may be rather extensive lesions in more than one bone without symptoms or serious impairment of function. The solitary lesions respond to curettage and packing with bone chips, but this procedure was not beneficial in treating ...
C. Zent Garber +2 more
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Experience with nine cases indicates that fibrous dysplasia of bone may present a variable clinical picture. In adults there may be rather extensive lesions in more than one bone without symptoms or serious impairment of function. The solitary lesions respond to curettage and packing with bone chips, but this procedure was not beneficial in treating ...
C. Zent Garber +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 Bone and Joint Surgery. British volume, 1962
1 . Twenty patients with fibrous dysplasia, confirmed histologically, are reported and discussed in regard to classification, etiology, pathogenesis and treatment. The various fibrous or fibrocystic lesions of bone are characterised briefly for purpose of contrast, and the position of fibrous dysplasia in this heterogeneous collection is suggested. 2.
Stewart Mj, Edmonson As, Gilmer Ws
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1 . Twenty patients with fibrous dysplasia, confirmed histologically, are reported and discussed in regard to classification, etiology, pathogenesis and treatment. The various fibrous or fibrocystic lesions of bone are characterised briefly for purpose of contrast, and the position of fibrous dysplasia in this heterogeneous collection is suggested. 2.
Stewart Mj, Edmonson As, Gilmer Ws
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Fibrous Dysplasia of Temporal Bone [PDF]
Archives of Otolaryngology - Head and Neck Surgery, 1967 WE ARE PRESENTING a rare instance of monostotic fibrous dysplasia primarily involving the temporal bone which by subsequent enlargement caused displacement of the mandible. Review of the literature reveals only three reported cases of monostotic fibrous dysplasia with primary temporal bone involvement.
Fred E. Aengst, Felix Shiffman
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Fibrous dysplasia of the facial bones
The American Journal of Surgery, 1961Abstract 1. 1. Eight cases of fibrous dysplasia involving the facial bones have been presented to illustrate some of the features of this disorder. 2. 2. Definitive diagnosis when a biopsy has been performed is recommended. 3. 3. Conservative management is the therapy of choice with observation, or curretage with or without bone chip ...
Alvin H. Harris +2 more
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Fibrous Dysplasia of the Temporal Bone
Otology & Neurotology, 2002Fibrous dysplasia is a rare, benign disease even though the clinical picture may appear severe. It presents a progressive replacement of normal bone structures by fibrous tissue, can involve one or more bone segments and, in some cases, it could be associated with skin lesions and endocrinopathies (McCune-Albright syndrome).
Chen Jm, Chee Gh
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Fibrous Dysplasia of Facial Bones [PDF]
Archives of Otolaryngology - Head and Neck Surgery, 1956 In 1938 Lichtenstein coined the phrase "fibrous dysplasia of bone" for a pathologicoanatomical entity which he wished to combine with, on the one hand, or separate, on the other hand, from lesions described in the literature under various designations.
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Seminars in Arthritis and Rheumatism, 2013
Fibrous dysplasia (FD) is caused by somatic mutations in GNAS and activation of the cAMP-regulating protein, Gs alpha ( gsp ). gsp inhibits differentiation of stem cells to mature osteogenic cells, resulting in replacement of normal bone with a highly proliferative stroma composed of cells that express osteogenic markers. Apoptosis follows, leaving
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Fibrous dysplasia (FD) is caused by somatic mutations in GNAS and activation of the cAMP-regulating protein, Gs alpha ( gsp ). gsp inhibits differentiation of stem cells to mature osteogenic cells, resulting in replacement of normal bone with a highly proliferative stroma composed of cells that express osteogenic markers. Apoptosis follows, leaving
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Polyostotic fibrous dysplasia of bone
Oral Surgery, Oral Medicine, Oral Pathology, 1958Present Illness.--The patient, a B-year-old white girl, was referred to this office by auother dentist on April 1, 1955, for removal of the upper and lower first and second deciduous molars, During the course of the examination, the entire clinical picture revealed itself (it will be presented in detail below).
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Fibrous Dysplasia of the Temporal Bone
Archives of Otolaryngology, 1969FIBROUS DYSPLASIA is a term coined by Lichtenstein and Jaffe 1 in 1942 to designate an ill-defined group of bony changes which were previously designated by such varying terms as osteogenic or ossifying fibroma, fibrous osteoma, or osteofibroma. The issue is whether these growths really represent tumors or are merely due to a failure of bone to heal in
Albert Cohen, Harry Rosenwasser
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