Results 211 to 220 of about 11,182 (240)
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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
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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 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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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
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: A case report
RGUHS Journal of Dental Sciences, 2020Fibrous 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
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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