Results 161 to 170 of about 2,105 (203)
Polyostotic Fibrous Dysplasia in a Dog [PDF]
Veterinary and Comparative Orthopaedics and Traumatology, 1998 SummaryA young Dobermann Pincher dog with severe right hind leg lameness was admitted to our clinic. A complete radiographic examination showed the presence of cystic lesions in the right tibia and femur and polyostotic fibrous dysplasia was diagnosed.The distal tibial lesion, associated with an incomplete cortical fracture, was treated by surgical ...
DI MEO, Antonio +3 more
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Craniofacial polyostotic fibrous dysplasia
Journal of Maxillofacial Surgery, 1985Three 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
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Proceedings of the Royal Society of Medicine, 1951
A case of polyostotic fibrous dysplasia in an African male is described. The case also had bilateral congenital cataracts and nerve deafness on the side affected by the dysplasia.
S, MEYERSOHN, I J, GREK
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A case of polyostotic fibrous dysplasia in an African male is described. The case also had bilateral congenital cataracts and nerve deafness on the side affected by the dysplasia.
S, MEYERSOHN, I J, GREK
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Polyostotic fibrous dysplasia involving the thoracic spine with myelopathy: case report and review of the literature [PDF]
Spine Journal, 2014 BACKGROUND CONTEXT: Polyostotic fibrous dysplasia (PFD) seldom involves the thoracic spine and usually presents with back pain. PURPOSE: To describe an extremely rare presentation of an uncommon disease.
Zhong Jun Liu +2 more
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Orthopedics, 2014
An 18-year-old man was referred to the authors’ institution’s thoracic cancer specialists for further consultation after abnormal findings were seen on chest radiograph.
Terrence C. Demos +4 more
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An 18-year-old man was referred to the authors’ institution’s thoracic cancer specialists for further consultation after abnormal findings were seen on chest radiograph.
Terrence C. Demos +4 more
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Familial polyostotic fibrous dysplasia
Oral Surgery, Oral Medicine, Oral Pathology, 1975A 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
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Polyostotic Fibrous Dysplasia And Acromegaly
Archives of Internal Medicine, 1964In 1937 Albright and co-workers1described a syndrome consisting of disseminated fibrous dysplasia of bones, cutaneous pigmentation, and precocious menstruation. There has been considerable interest in this syndrome since that time because of its unexplained pathogenesis and relationship between the endocrine abnormality and the bone disease.
M T, SCURRY, J M, BICKNELL, S S, FAJANS
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Polyostotic Fibrous Dysplasia and Acromegaly
Journal of Pediatric Orthopaedics, 1991A 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
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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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The British Journal of Radiology, 1953
A case of polyostotic fibrous dysplasia in an African female is described. The case also had bilateral loss of smell sense and involvement of left paranasal sinuses, but no evidence of hormonal derangement or other changes in the skeleton.
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A case of polyostotic fibrous dysplasia in an African female is described. The case also had bilateral loss of smell sense and involvement of left paranasal sinuses, but no evidence of hormonal derangement or other changes in the skeleton.
openaire +2 more sources