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基于 2017 年 WHO 分类的垂体腺瘤分类。

Delineating the Spectrum of Pituitary Adenoma Based on the WHO 2017 Classification.

机构信息

Department of Neuropathology, National Institute of Mental Health and Neurosciences, Bengaluru, Karnataka, India.

出版信息

Neurol India. 2024 Jan 1;72(1):96-101. doi: 10.4103/neuroindia.NI_913_20. Epub 2024 Feb 29.

Abstract

BACKGROUND

The WHO 2017 classification of endocrine tumors incorporates lineage-specific transcription factors (TF) and hormone expression for the classification of pituitary adenoma (PA). There is paucity of reports describing the spectrum of PA based on this classification.

OBJECTIVE

The aim of this study was to delineate the spectrum of PA based on WHO 2017 classification of endocrine tumors.

MATERIALS AND METHODS

PA diagnosed in the year 2018 were studied. H and E and hormonal immunohistochemistry (IHC) for GH, PRL, ACTH, TSH, FSH, LH, CK, T-Pit and MIB-1 were performed and the results were analyzed.

RESULTS

The cohort included 88 cases. M: F ratio was 2:1. Clinically, 22 (25%) were functional and 66 (75%) were non-functional adenomas. Amongst the clinically functional adenomas, GH secreting adenomas were the commonest (68%). Majority (83%) of non-functional adenomas were hormone positive with gonadotroph adenomas being the commonest (72.7%). Eleven (12.5%) PA were clinically and hormonally silent. Three of these showed intense nuclear T-Pit positivity, classifying them under silent corticotroph adenoma. Lineage of the remaining eight adenomas remained undetermined, since, IHC for Pit-1 and SF-1 was not performed. The aggressive adenomas identified by IHC included sparsely granulated somatotroph adenoma, Crooke cell adenoma, silent corticotroph adenoma, densely granulated lactotroph adenoma in men and constituted 17% of the PA. Four (4/88) cases were clinically invasive.

CONCLUSION

A large majority of PA including aggressive adenomas can be identified by IHC. Addition of T-Pit helped to identify silent corticotroph adenoma. Pit -1 and SF-1 TF would help identify plurihormonal Pit-1 PA and null cell adenomas.

摘要

背景

世界卫生组织 2017 年内分泌肿瘤分类纳入了谱系特异性转录因子(TF)和激素表达,用于垂体腺瘤(PA)的分类。基于这一分类,描述 PA 谱的报道很少。

目的

本研究旨在根据世界卫生组织 2017 年内分泌肿瘤分类来描绘 PA 的谱。

材料和方法

研究了 2018 年诊断的 PA。进行了 H&E 和 GH、PRL、ACTH、TSH、FSH、LH、CK、T-Pit 和 MIB-1 的激素免疫组织化学(IHC),并对结果进行了分析。

结果

该队列包括 88 例患者。M:F 比例为 2:1。临床上,22 例(25%)为功能性腺瘤,66 例(75%)为非功能性腺瘤。在临床上功能性腺瘤中,GH 分泌腺瘤最常见(68%)。大多数(83%)非功能性腺瘤为激素阳性,其中促性腺激素腺瘤最常见(72.7%)。11 例(12.5%)PA 临床上和激素上均无活性。其中 3 例显示强烈的核 T-Pit 阳性,将其归类为无活性促肾上腺皮质激素腺瘤。由于未进行 Pit-1 和 SF-1 的 IHC,其余 8 例腺瘤的谱系仍未确定。通过 IHC 确定的侵袭性腺瘤包括稀疏颗粒生长激素腺瘤、Crooke 细胞腺瘤、无活性促肾上腺皮质激素腺瘤、男性致密颗粒催乳素腺瘤,占 PA 的 17%。4 例(4/88)为临床侵袭性。

结论

大多数 PA,包括侵袭性腺瘤,都可以通过 IHC 识别。添加 T-Pit 有助于识别无活性促肾上腺皮质激素腺瘤。Pit-1 和 SF-1 TF 将有助于识别多激素 Pit-1 PA 和无细胞腺瘤。

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