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Radiology, 1943
In the course of our examination of candidates for induction into the United States Army an example of a rather rare clinical syndrome was encountered. While this disease has been described in the literature under a variety of names, the one suggested by Lichtenstein (1)—polyostotic fibrous dysplasia—appears satisfactory and has been adopted in ...
Lewis E. Etter, John W. Hurst
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In the course of our examination of candidates for induction into the United States Army an example of a rather rare clinical syndrome was encountered. While this disease has been described in the literature under a variety of names, the one suggested by Lichtenstein (1)—polyostotic fibrous dysplasia—appears satisfactory and has been adopted in ...
Lewis E. Etter, John W. Hurst
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Endocrine Practice, 2019
OBJECTIVE Fibrous dysplasia (FD) is a rare disorder characterized by pain, deformity, and pathologic fractures. McCune-Albright syndrome (MAS) includes a combination of FD, hyperfunctional endocrinopathy, and/or café-au-lait pigmentation.
Yabing Wang +6 more
semanticscholar +1 more source
OBJECTIVE Fibrous dysplasia (FD) is a rare disorder characterized by pain, deformity, and pathologic fractures. McCune-Albright syndrome (MAS) includes a combination of FD, hyperfunctional endocrinopathy, and/or café-au-lait pigmentation.
Yabing Wang +6 more
semanticscholar +1 more source
Polyostotic Fibrous Dysplasia in a Dog
Veterinary and Comparative Orthopaedics and Traumatology, 1998SummaryA 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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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.
Stefan S. Fajans +2 more
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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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Scintigraphic Evaluation of Polyostotic Fibrous Dysplasia
Clinical Nuclear Medicine, 1987Bone scintigraphy is a sensitive imaging modality for detecting early lesions and polyostotic involvement in fibrous dysplasia. Common findings include multiple areas of focal uptake that are often unilateral and typically involve the ribs, tibia, femur, and craniofacial bones.
Shiv M. Gupta +2 more
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Peptiduria in polyostotic fibrous dysplasia
Biochemical Medicine, 1971Abstract Peptiduria has been observed in two children, a male with polyostotic fibrous dysplasia and a female with the McCune-Albright syndrome. Urine from both patients contained relatively large amounts of a unique array of nine unusual ninhydrin-positive compounds which may be distinctive for their clinical condition.
Kenneth N.F. Shaw +5 more
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Malignant Transformation of Polyostotic Fibrous Dysplasia
Southern Medical Journal, 1979We have described an unusual case of polyostotic fibrous dysplasia in a 25-year-old white woman who had malignant transformation into a mesenchymal tumor with widespread metastases and features of rhabdomyosarcoma. Masculinization also occurred with high plasma testosterone levels. A mechanism for the development of masculinizing features is discussed.
Gottlieb Li, Johnson Cb, Gilbert Ef
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Polyostotic fibrous dysplasia involving the sternum
Clinical Rheumatology, 1988The authors present a case of polyostotic fibrous dysplasia involving the sternum as well. The case is well supported the strumental and histological point of view.
Zorzin, L +3 more
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An extensive type of polyostotic fibrous dysplasia [PDF]
Pediatric Radiology, 1997 The case describes an 11-year-old girl affected by an unusually extensive type of polyostotic fibrous dysplasia. The cranium and face and both femurs, tibias, and fibulas were extensively and almost symmetrically involved. Tubulation deformities were noted in the metacarpals and middle phalanges of both hands.
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