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[激活型GNAS突变:骨纤维发育不良、其相关综合征及其他骨骼和骨骼外病变的综述]

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

作者信息

Ostertag H, Glombitza S

机构信息

Pathologisches Institut, Klinikum Region Hannover, Haltenhoffstraße 41, 30167, Hannover, Deutschland.

出版信息

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

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.

摘要

骨纤维发育不良是一种先天性而非遗传性疾病,有单骨型或多骨型表现,可能与骨骼外疾病McCune - Albright综合征相关,或与骨骼肌黏液瘤(称为Mazabraud综合征)相关。反复染色体畸变的证实可能导致这样的结论:骨纤维发育不良是一种肿瘤形成,而非发育异常的骨骼疾病。所有所述疾病的主要病因是GNAS激活突变,几乎在所有病变中都可检测到。对这种突变影响的研究增进了对这些迄今为止仅通过描述性定义的疾病的理解,也使得更容易区分各种纤维性骨病变。目前的见解表明,这种突变在其他骨骼外肿瘤形成中可能也起关键作用。

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