多激素垂体腺瘤亚型的临床特征。

Christie G Turin, Katja Kiseljak-Vassiliades, Margaret E Wierman, Kevin Lillehei, B K Kleinschmidt-DeMasters
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引用次数: 0

摘要

多激素垂体神经内分泌肿瘤/垂体腺瘤(PitNET/PAs)表达多种激素和/或转录因子。多激素肿瘤中最常见的两种亚型是未成熟的PIT-1(垂体特异性poo -class同源结构域因子-1)谱系肿瘤和成熟的PIT-1多激素肿瘤,其中大多数肿瘤显示PIT-1/SF-1(甾体生成因子1)共表达。我们的目的是在人口学、放射学、神经外科和内分泌学特征方面对这两种PIT-1多激素肿瘤类型进行直接比较。对2018年至2024年间接受切除术的多激素PitNET/PAs患者进行数据库检索和图表回顾。共鉴定出26个多激素PitNET/PAs(12个未成熟的PIT-1谱系,14个成熟的PIT-1/SF-1共表达者)。未成熟的PIT-1谱系肿瘤大于成熟的PIT-1/SF-1共表达者(中位尺寸27.5 mm vs 16 mm, p=0.02)。两组在性别(女性67%对50%)、中位年龄(45对50岁)、激素活性(83%对79%)、海绵窦侵袭(各50%)、术后残留肿瘤(55%对43%)或复发率(9%对7%)方面均无显著差异。与成熟的PIT-1/SF-1共表达物相比,未成熟的PIT-1谱系肿瘤倾向于更高的Ki-67水平(30%对0%,p=0.21),以及手术后激素过量的药物治疗需求(33%对7%,p=0.15),但这没有统计学意义。总之,与成熟的PIT-1/SF-1共表达者相比,未成熟的PIT-1谱系肿瘤表现出更大的体积,并且对术后药物治疗的需求增加,这强调了仔细的组织学分析的重要性。相反,这两种多激素亚型术前不能通过性别、年龄或激素谱来预测。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Clinical Features of Plurihormonal Pituitary Adenoma Subtypes.

Plurihormonal pituitary neuroendocrine tumors/pituitary adenomas (PitNET/PAs) express multiple hormones and/or transcription factors. The two most common subtypes within the plurihormonal category are immature PIT-1 (pituitary-specific POU-class homeodomain factor-1) lineage tumors and mature PIT-1 plurihormonal tumors, most of which show PIT-1/SF-1 (steroidogenic factor 1) co-expression. Our aim is to provide direct comparison between these two PIT-1 plurihormonal tumor types in terms of demographic, radiological, neurosurgical, and endocrinological features. A database search and chart review of patients with plurihormonal PitNET/PAs who underwent resection between 2018 and 2024 was performed. Twenty-six plurihormonal PitNET/PAs (12 immature PIT-1-lineage, 14 mature PIT-1/SF-1 co-expressors) were identified. Immature PIT-1 lineage tumors were larger than mature PIT-1/SF-1 co-expressors (median size 27.5 mm vs 16 mm, p=0.02). No significant differences were detected between the two groups in terms of gender (females 67% vs. 50%), median age (45 vs 50 years), hormonal activity (83% vs 79%), invasion of the cavernous sinuses (50% each), residual tumor after surgery (55% vs 43%) or rate of recurrence (9% vs 7%), respectively. Immature PIT-1 lineage tumors trended towards higher Ki-67 levels when compared to mature PIT-1/SF-1 co-expressors (30% vs 0%, p=0.21) as well as need for medical therapy after surgery for hormone excess (33% vs 7%, p=0.15) but this was not statistically significant. In conclusion, immature PIT-1 lineage tumors exhibit larger size and an increased requirement for postoperative medical therapy than mature PIT-1/SF-1 co-expressors, underscoring the usefulness of careful histologic analysis. In contrast, these two plurihormonal subtypes cannot be predicted pre-operatively by gender, age, or hormonal profile.

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