[The activating GNAS mutation : A survey of fibrous dysplasia, its associated syndromes, and other skeletal and extraskeletal lesions]

Pathologe. 2018 Mar;39(2):146-153. doi: 10.1007/s00292-018-0417-y.
[Article in German]

Abstract

Fibrous dysplasia of bone is a connatal but not hereditary disease with monostotic or polyostotic manifestations and may be associated either with the extraskeletal disease McCune-Albright syndrome or with myxoma of the skeletal muscle, termed Mazabraud syndrome.The confirmation of recurrent chromosomal aberrations may lead to the conclusion that fibrous dysplasia is a neoplasia rather than a dysplastic skeletal disease.The primary cause of all forms of the described diseases is the activating GNAS mutation, which is detectable in almost all lesions. Research into the impact of this mutation has increased the understanding of these up to now solely descriptively defined diseases and also allowed easier discrimination of various fibro-osseous skeletal lesions. Current insights suggest that this mutation may also play a pivotal role in other extraskeletal neoplasias.

Keywords: Chromosomal aberration; Fibrous Dysplasia; GNAS; Mazabraud; McCune Albright; Mutation; Myxoma.

Publication types

  • Review

MeSH terms

  • Chromogranins / genetics*
  • Fibrous Dysplasia, Polyostotic*
  • GTP-Binding Protein alpha Subunits, Gs / genetics*
  • Humans
  • Muscle Neoplasms*
  • Mutation
  • Surveys and Questionnaires

Substances

  • Chromogranins
  • GNAS protein, human
  • GTP-Binding Protein alpha Subunits, Gs