Results 241 to 250 of about 11,914 (280)
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The Role of Staged Cryosurgery and Three-Dimensional Computed Tomography Integrated Navigation System in the Surgical Management of Severe Involvement of Craniofacial Polyostotic Fibrous Dysplasia.

The Journal of craniofacial surgery (Print), 2020
Fibrous dysplasia (FD) is a developmental bone disorder caused by the hamartamatous proliferation of bone-forming cells. A 29-year-old male patient with diagnosis of FD was admitted to our clinic with the symptoms of severe craniomaxillofacial ...
Kemalettin Yildiz   +5 more
semanticscholar   +1 more source

Polyostotic Fibrous Dysplasia

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.
openaire   +3 more sources

Craniofacial polyostotic fibrous dysplasia

Journal of Maxillofacial Surgery, 1985
Three cases of gross craniofacial polyostotic fibrous dysplasia are presented, together with a brief review of the condition, and pertinent points regarding the cases are discussed. As complete excision of the lesion and immediate reconstruction is rarely feasible or possible, and partial excision may result in accelerated growth of the lesion during ...
Owen C. Sparrow, Glenn E. Lello
openaire   +3 more sources

Polyostotic Fibrous Dysplasia Mimicking Bone Involvement in Hodgkin Lymphoma: A Pediatric Case and Literature Review

Acta Haematologica, 2020
Bone involvement in Hodgkin lymphoma (HL) is rare. The differential diagnosis between HL bone localization and other malignant or benign skeletal diseases is challenging.
G. Lapietra   +9 more
semanticscholar   +1 more source

Polyostotic Fibrous Dysplasia and Acromegaly

Journal of Pediatric Orthopaedics, 1991
A review of the recent orthopaedic literature reveals little information on the endocrinopathic associations of polyostotic fibrous dysplasia. This article illustrates the need for endocrinologic evaluations at both initial diagnosis and at follow-up examinations. Two patients with polyostotic fibrous dysplasia and acromegaly are presented.
P. C. Kupcha   +3 more
openaire   +3 more sources

Polyostotic fibrous dysplasia

Irish Journal of Medical Science, 1944
A fairly typical example of polyostotic fibrous dysplasia is recorded in a girl of 4 1/2 years. There were some unusual features about the patient, such as retarded mental development, very extensive lesions in the bones, predominance of cartilage in bone biopsy and anaemia with nucleated red cells in the peripheral blood.
F. Duff   +3 more
openaire   +2 more sources

Polyostotic fibrous dysplasia: A case report

RGUHS Journal of Dental Sciences, 2020
Fibrous dysplasia (FD) is a fibro-osseous anomaly, where in normal bone is substituted with fibrous stroma. It is of unknown etiology but recently reported to be associated with mutation in GNAS1 gene (20q13.2) and consists of three subtypes monostotic ...

semanticscholar   +1 more source

Jaffe Lichtenstein Type of Polyostotic Skeletal Fibrous Dysplasia With the Involvement of Cranial Bones.

The Journal of craniofacial surgery (Print), 2021
Fibrous dysplasia (FD), a benign fibro-osseous bone tumor commonly involving the craniofacial region, presents a wide spectrum of radiographic patterns.
O. Akkemik   +3 more
semanticscholar   +1 more source

Polyostotic fibrous dysplasia

Indian Journal of Otolaryngology, 1966
A case of fibrous dysplasia of polyostotic variety involving cervical spines, both sides of occipital bone besides mandible, maxilla, parietal, humerus, ulna, and radius of the left side is presented and briefly discussed.
Prem K. Kakar   +2 more
openaire   +2 more sources

Familial polyostotic fibrous dysplasia

Oral Surgery, Oral Medicine, Oral Pathology, 1975
A case of polyostotic fibrous dysplasia of the craniofacial type is presented, together with substantial evidence that this condition had a genetic basis in this patient. A review of the literature indicates that there is absolutely no previous evidence of a genetic basis to this condition.
M. Reitzik, J.F. Lownie
openaire   +2 more sources

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