2001
DOI: 10.1053/ajot.2001.24829
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Fibrous dysplasia, chondrosarcoma, and McCune-Albright syndrome

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Cited by 30 publications
(20 citation statements)
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“…McCune and Bruch and Albright and co-workers in separate publications mentioned about the term osteodystrophia fi brosa disseminate, characterized by endocrinopathies, cutaneous hyperpigmentation and precocious puberty in females in 1937. [1] In the following year Lichtenstein coined the terms fi brous dysplasia and polyostotic fi brous dysplasia.…”
Section: Discussionmentioning
confidence: 99%
See 1 more Smart Citation
“…McCune and Bruch and Albright and co-workers in separate publications mentioned about the term osteodystrophia fi brosa disseminate, characterized by endocrinopathies, cutaneous hyperpigmentation and precocious puberty in females in 1937. [1] In the following year Lichtenstein coined the terms fi brous dysplasia and polyostotic fi brous dysplasia.…”
Section: Discussionmentioning
confidence: 99%
“…It occurs as one of three clinical patterns: [1] involvement of a single bone (monostotic); [2] involvement of multiple bones (polyostotic) and [3] polyostotic disease, associated with café au lait skin pigmentations and endocrine abnormalities, especially precocious puberty (McCune-Albright syndrome). Management of temporal bone fibrous dysplasia is conservative.…”
Section: Introductionmentioning
confidence: 99%
“…A traumatic etiology has been suggested but not widely supported [14]. Malignant transformation within a focus of fibrous dysplasia is very infrequent [15]. The prevalence of sarcomatous changes has been reported to be 0.4% [16, 17].…”
Section: Discussionmentioning
confidence: 99%
“…Eine seltene Sonderform der polyostotischen FD mit einer Inzidenz von 3 % aller Fälle mit FD wird als McCune-Albright-Syndrom bezeichnet. Hierbei imponiert klinisch eine Trias aus der polyostotischen Variante der FD, Pigmentanomalien meist in Form von CafØ-au-lait-Flecken, eventuell auch an Lippen-und Mundschleimhaut sowie Endokrinopathien, beispielsweise im Sinne einer Pubertas praecox oder Akromegalie [2,18,19]. Differenzialdiagnostisch kommen zahlreiche andere gutartige Knochenerkrankungen wie Fibrome, Chondrome oder der Morbus Paget in Betracht [5,8,15].…”
Section: Patienten Und Methodenunclassified
“…Die Ätiologie der Fibrösen Dysplasie (FD) im Gesichtsschädelbereich gilt immer noch als nicht restlos aufgeklärt. Die mit 1 : 4000 -10 000 äu-ßerst geringe Zahl von Erkrankungsfällen mag hierfür einer der Gründe sein [1,2]. Pathophysiologisch wird die FD als eine mesenchymale Knochenentwicklungsstörung gedeutet [3].…”
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