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多激素阳性垂体腺瘤:系统评价和单中心系列研究。

Plurihormonal PIT-1-Positive Pituitary Adenomas: A Systematic Review and Single-Center Series.

机构信息

Department of Neurological Surgery, University of California, San Francisco, School of Medicine, San Francisco, California, USA.

Department of Pathology, University of California, San Francisco, School of Medicine, San Francisco, California, USA.

出版信息

World Neurosurg. 2021 Jul;151:e185-e191. doi: 10.1016/j.wneu.2021.04.003. Epub 2021 Apr 20.

Abstract

OBJECTIVE

The 2017 World Health Organization classification of pituitary adenomas identified the plurihormonal PIT-1-positive (PP1) adenoma as a distinct subtype. The reported data suggest that PP1 adenomas encompass the former class of silent subtype 3 (SS3) adenomas and might have an aggressive phenotype. In the present study, we summarized the current clinical data on PP1 and SS3 adenomas and compared the reported data with the data from a single institutional cohort.

METHODS

Medline and Google Scholar were searched from 1990 to 2020 for clinical series of PP1 and SS3 adenomas in accordance with the PRISMA (preferred reporting items for systematic reviews and meta-analyses) guidelines. Studies were included if they had reported pituitary pathology as PP1 or SS3 adenomas and had reported the clinical outcomes after surgical intervention. To better define the PP1 phenotype compared with non-PP1 adenomas, we also reviewed the adenomas treated surgically at our institution from 2012 to 2019.

RESULTS

Of all the tumors reported in the studies as PP1 or SS3, 99% were macroadenomas and 18% were giant adenomas (>4 cm). Of the reported patients, 31.8% had received radiotherapy, and 22.9% had undergone multiple surgeries for their pituitary tumor. In our single-center experience, 20 patients had an adenoma that met the criteria for a PP1 adenoma. Compared with the 1146 non-PP1 tumors, the PP1 tumors did not show statistically significant differences in the extent of resection, size, number of previous surgeries, future reoperations, rate of radiotherapy, p53 staining, or MIB-1 labeling index.

CONCLUSIONS

The findings from the present large, single-center study comparing PP1 and non-PP1 adenomas do not suggest that PP1 tumors are more aggressive. Further work is warranted to identify the pathologic subtypes of pituitary adenomas that are consistently more clinically aggressive.

摘要

目的

2017 年世界卫生组织(WHO)对垂体腺瘤的分类将 PIT-1 阳性(PP1)多激素腺瘤确定为一种独特的亚型。报告的数据表明,PP1 腺瘤包含了前一类静默亚型 3(SS3)腺瘤,并且可能具有侵袭性表型。在本研究中,我们总结了目前关于 PP1 和 SS3 腺瘤的临床数据,并将报告的数据与单机构队列的数据进行了比较。

方法

根据 PRISMA(系统评价和荟萃分析的首选报告项目)指南,我们在 Medline 和 Google Scholar 上检索了 1990 年至 2020 年关于 PP1 和 SS3 腺瘤的临床系列研究。如果研究报告了垂体病理学为 PP1 或 SS3 腺瘤,并报告了手术干预后的临床结果,则纳入研究。为了更好地定义 PP1 表型与非 PP1 腺瘤的区别,我们还回顾了我们机构在 2012 年至 2019 年期间接受手术治疗的腺瘤。

结果

在所报道的作为 PP1 或 SS3 的所有肿瘤中,99%为大腺瘤,18%为巨大腺瘤(>4cm)。在报告的患者中,31.8%接受了放疗,22.9%因垂体瘤接受了多次手术。在我们的单中心经验中,有 20 例患者的腺瘤符合 PP1 腺瘤的标准。与 1146 例非 PP1 肿瘤相比,PP1 肿瘤在切除程度、大小、术前手术次数、未来再次手术、放疗率、p53 染色或 MIB-1 标记指数方面均无统计学差异。

结论

本项来自大型单中心研究比较 PP1 和非 PP1 腺瘤的结果表明,PP1 肿瘤并不具有更强的侵袭性。进一步的工作需要确定在临床上更具侵袭性的垂体腺瘤的病理亚型。

相似文献

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Atypical pituitary adenoma: a clinicopathologic case series.非典型垂体腺瘤:临床病理病例系列。
J Neurosurg. 2018 Apr;128(4):1058-1065. doi: 10.3171/2016.12.JNS162126. Epub 2017 Jun 9.

本文引用的文献

1
Aggressive Pituitary Adenomas and Carcinomas.侵袭性垂体腺瘤和腺癌。
Endocrinol Metab Clin North Am. 2020 Sep;49(3):505-515. doi: 10.1016/j.ecl.2020.05.008. Epub 2020 Jul 8.
2
Definition and diagnosis of aggressive pituitary tumors.侵袭性垂体瘤的定义和诊断。
Rev Endocr Metab Disord. 2020 Jun;21(2):203-208. doi: 10.1007/s11154-019-09531-x.
7

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