Literature DB >> 23858622

Fibrous dysplasia.

Steven A Lietman1, Michael A Levine.   

Abstract

Fibrous dysplasia is a developmental abnormality of bone that is characterized by a highly disorganized mixture of immature fibrous tissue and fragments of immature trabecular bone. Fibrous dysplasia may arise as a single, discrete (monostotic) lesion or can occur with a more widespread distribution with multiple lesions that affect many bones (oligo- or polyostotic). Fibrous dysplasia is usually an isolated skeletal finding but can sometimes occur as a component of a multisystem developmental disorder known as McCune-Albright syndrome (MAS) that is also associated with endocrine hyperfunction (e.g. precocious puberty) and caf au lait cutaneous macules. The identification of activating mutations in GNAS in a subset of human GH-secreting pituitary tumors and autonomously functioning human thyroid tumors provided the initial basis for understanding the molecular pathophysiology of McCune-Albright syndrome and fibrous dysplasia. These observations led to the concept that activating mutations of the GNAS gene convert it into a putative oncogene referred to as gsp (Gsa or Gas). The classic radiographic feature of fibrous dysplasia is a hazy, radiolucent, or ground-glass, pattern resulting from the defective mineralization of immature dysplastic bone; it is usually strikingly different from the radiographic appearance of normal bone, calcified cartilage, or soft tissue. The surgical approach to fibrous dysplasia should in general be conservative. Recent research suggests that the WntlB-catenin pathway may play a role in fibrous dysplasia as patients with activating GNAS mutations specifically showed that Gas mutations activated Wnt/B-catenin signaling. Thus inhibition of 8-catenin signaling or silencing GNAS alleles that encode constitutively active Gsa molecules in fibrous dysplasia and McCune-Albright syndrome offer potential therapeutic promise and deserve further study. In summary fibrous dysplasia is a developmental abnormality of bone with a known molecular etiology; Further knowledge about the molecular pathology of fibrous dysplasia may lead to improved conservative therapies in the near future.

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Mesh:

Year:  2013        PMID: 23858622

Source DB:  PubMed          Journal:  Pediatr Endocrinol Rev        ISSN: 1565-4753


  8 in total

1.  Gene expression profiling of craniofacial fibrous dysplasia reveals ADAMTS2 overexpression as a potential marker.

Authors:  Shang-Hui Zhou; Wen-Jun Yang; Sheng-Wen Liu; Jiang Li; Chun-Ye Zhang; Yun Zhu; Chen-Ping Zhang
Journal:  Int J Clin Exp Pathol       Date:  2014-12-01

2.  Treatment of Girls and Boys with McCune-Albright Syndrome with Precocious Puberty - Update 2017.

Authors:  Anna Neyman; Erica A Eugster
Journal:  Pediatr Endocrinol Rev       Date:  2017-12

Review 3.  Wnts' fashion statement: from body stature to dysplasia.

Authors:  Deepti Malhotra; Yingzi Yang
Journal:  Bonekey Rep       Date:  2014-06-11

4.  Disrupted bone remodeling leads to cochlear overgrowth and hearing loss in a mouse model of fibrous dysplasia.

Authors:  Omar Akil; Faith Hall-Glenn; Jolie Chang; Alfred Li; Wenhan Chang; Lawrence R Lustig; Tamara Alliston; Edward C Hsiao
Journal:  PLoS One       Date:  2014-05-01       Impact factor: 3.240

5.  Monostotic fibrous dysplasia presenting in maxilla: a case report.

Authors:  Taha Emre Kose; Onur Dincer Kose; Mehmet Ali Erdem; Abdulkadir Burak Cankaya; Ilknur Ozcan Duman
Journal:  J Istanb Univ Fac Dent       Date:  2016-04-01

6.  Response to Zoledronic Acid Infusion in Children With Fibrous Dysplasia.

Authors:  Sujit Kumar Tripathy; Shakti Swaroop; Sandeep Velagada; Debashree Priyadarshini; Rashmi Ranjan Das; Amit Kumar Satpathy; Kanhaiyalal Agrawal
Journal:  Front Pediatr       Date:  2020-11-24       Impact factor: 3.418

7.  Surgical Treatment of Fibrous dysplasia in the Maxillary Bone of a 12 Year-Old Girl: A Case Report.

Authors:  Sahand Samieirad; Mohammad Mehdi Momtaz; Nooshin Mohtasham; Farzaneh Mohammadzadeh; Niloofar Ebrahimzadeh; Elahe Tohidi
Journal:  World J Plast Surg       Date:  2021-09

Review 8.  Genetics and Epigenetics of Bone Remodeling and Metabolic Bone Diseases.

Authors:  Lucia Oton-Gonzalez; Chiara Mazziotta; Maria Rosa Iaquinta; Elisa Mazzoni; Riccardo Nocini; Lorenzo Trevisiol; Antonio D'Agostino; Mauro Tognon; John Charles Rotondo; Fernanda Martini
Journal:  Int J Mol Sci       Date:  2022-01-28       Impact factor: 5.923

  8 in total

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