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促性腺激素细胞肿瘤

Gonadotrope Tumors.

作者信息

Asa S L, Ezzat S

机构信息

Department of Laboratory Medicine and Pathobiology, University of Toronto, Toronto, ON, Canada; Department of Pathology, Laboratory Medicine Program, University Health Network, Toronto, ON, Canada.

Department of Medicine, University of Toronto, Endocrine Oncology, Princess Margaret Cancer Centre, University Health Network, Toronto, ON, Canada.

出版信息

Prog Mol Biol Transl Sci. 2016;143:187-210. doi: 10.1016/bs.pmbts.2016.08.005. Epub 2016 Sep 7.

Abstract

Gonadotrope tumors arise from the gonadotropes of the adenohypophysis. These cells rarely give rise to hyperplasia, usually only in the setting of long-standing premature gonadal failure. In contrast, gonadotrope tumors represent one of the most frequent types of pituitary tumors. Despite their relatively common occurrence, the pathogenesis of gonadotrope tumors remains unknown. Effective nonsurgical therapies remain out of reach. We review the pituitary gonadotrope from the morphologic and functional perspectives to better understand its involvement as the cell of origin of a frequent type of pituitary tumor.

摘要

促性腺激素细胞肿瘤起源于腺垂体的促性腺激素细胞。这些细胞很少发生增生,通常仅在长期存在的性腺功能早衰情况下才会出现。相比之下,促性腺激素细胞肿瘤是最常见的垂体肿瘤类型之一。尽管其相对常见,但促性腺激素细胞肿瘤的发病机制仍不清楚。有效的非手术治疗方法仍然难以实现。我们从形态学和功能角度对垂体促性腺激素细胞进行综述,以更好地了解其作为一种常见垂体肿瘤起源细胞的情况。

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