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分泌生长激素和促肾上腺皮质激素的垂体腺瘤:一项组织学、免疫细胞化学、电子显微镜及原位杂交研究。病例报告。

Pituitary adenoma producing growth hormone and adrenocorticotropin: a histological, immunocytochemical, electron microscopic, and in situ hybridization study. Case report.

作者信息

Kovacs K, Horvath E, Stefaneanu L, Bilbao J, Singer W, Muller P J, Thapar K, Stone E

机构信息

Department of Laboratory Medicine, St. Michael's Hospital, University of Toronto, Ontario, Canada.

出版信息

J Neurosurg. 1998 Jun;88(6):1111-5. doi: 10.3171/jns.1998.88.6.1111.

Abstract

The authors report on the morphological features of a pituitary adenoma that produced growth hormone (GH) and adrenocorticotropic hormone (ACTH). This hormone combination produced by a single adenoma is extremely rare; a review of the available literature showed that only one previous case has been published. The tumor, which was removed from a 62-year-old man with acromegaly, was studied by histological and immunocytochemical analyses, transmission electron microscopy, immunoelectron microscopy, and in situ hybridization. When the authors used light microscopy, the tumor appeared to be a bimorphous mixed pituitary adenoma composed of two separate cell types: one cell population synthesized GH and the other ACTH. The cytogenesis of pituitary adenomas that produce more than one hormone is obscure. It may be that two separate cells--one somatotroph and one corticotroph--transformed into neoplastic cells, or that the adenoma arose in a common stem cell that differentiated into two separate cell types. In this case immunoelectron microscopy conclusively demonstrated ACTH in the secretory granules of several somatotrophs. This was associated with a change in the morphological characteristics of secretory granules. Thus it is possible that the tumor was originally a somatotropic adenoma that began to produce ACTH as a result of mutations that occurred during tumor progression.

摘要

作者报告了一例分泌生长激素(GH)和促肾上腺皮质激素(ACTH)的垂体腺瘤的形态学特征。由单一腺瘤产生的这种激素组合极为罕见;对现有文献的回顾显示,此前仅发表过一例相关病例。该肿瘤取自一名患有肢端肥大症的62岁男性,通过组织学和免疫细胞化学分析、透射电子显微镜、免疫电子显微镜及原位杂交进行研究。作者使用光学显微镜观察时,肿瘤似乎是一种双形态混合垂体腺瘤,由两种不同的细胞类型组成:一种细胞群体合成GH,另一种合成ACTH。分泌多种激素的垂体腺瘤的细胞发生机制尚不清楚。可能是两个独立的细胞——一个生长激素细胞和一个促肾上腺皮质激素细胞——转变为肿瘤细胞,或者腺瘤起源于一个分化为两种不同细胞类型的共同干细胞。在该病例中,免疫电子显微镜确凿地证实在一些生长激素细胞的分泌颗粒中有ACTH。这与分泌颗粒形态特征的改变有关。因此,该肿瘤有可能原本是一种生长激素腺瘤,在肿瘤进展过程中由于发生突变而开始分泌ACTH。

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