功能性皮质营养瘤的肉芽形态与肿瘤大小、增殖活性、T2强度与白质比值以及手术后早期生化缓解相关。

IF 11.3 2区 医学 Q1 ENDOCRINOLOGY & METABOLISM
Endocrine Pathology Pub Date : 2024-09-01 Epub Date: 2024-07-24 DOI:10.1007/s12022-024-09819-y
Elif Tutku Durmuş, Mehmet Kefeli, Ozgur Mete, Sultan Çalışkan, Kerim Aslan, Mustafa Arda Onar, Ramis Çolak, Buğra Durmuş, Cengiz Cokluk, Ayşegül Atmaca
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引用次数: 0

摘要

与体细胞瘤不同,在大多数临床系列中,关于功能性 TPIT 系垂体神经内分泌肿瘤(促皮质素瘤)肿瘤肉芽形态相关性的数据记录并不统一。本研究评估了 41 例特征明确的功能性皮质营养瘤的特征,其中包括 28 例密颗粒皮质营养瘤(DGCTs)和 13 例疏颗粒皮质营养瘤(SGCTs),涉及术前临床和放射学检查结果、肿瘤增殖活性(包括有丝分裂计数和 Ki-67 标记指数)以及术后早期生化缓解率。SGCT组的肿瘤中位数(四分位间距(IQR))明显大于DGCT组[SGCT为16.00(16.00)毫米,DGCT为8.5(9.75)毫米,P = 0.049]。T2加权信号强度和T2强度(定量)在肿瘤肉芽的基础上没有统计学意义;但是,SGCT的T2强度与白质比值明显更高(P = 0.049)。DGCT组的Ki-67标记指数中位数(IQR)为2.00%(IQR为1.00%),SGCT组为4.00%(IQR为7.00%)(p = 0.043)。SGCT 组每 2 平方毫米的有丝分裂计数更高(p = 0.001)。在多变量分析中,无论肿瘤大小和增殖活性如何,稀疏肉芽模式(SGCT)仍是早期生化缓解概率较低的独立预测因子(p = 0.012)。目前的研究进一步证实了肿瘤肉芽模式作为一个生物变量的影响,并认为有必要按照世界卫生组织垂体神经内分泌肿瘤分类的指示,对功能性皮质营养肿瘤进行详细的组织学亚型分类。更重要的是,定量 T2 强度与白质比值的评估可作为 SGCT 的术前放射学预兆。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Granulation Patterns of Functional Corticotroph Tumors Correlate with Tumor Size, Proliferative Activity, T2 Intensity-to-White Matter Ratio, and Postsurgical Early Biochemical Remission.

Granulation Patterns of Functional Corticotroph Tumors Correlate with Tumor Size, Proliferative Activity, T2 Intensity-to-White Matter Ratio, and Postsurgical Early Biochemical Remission.

Unlike somatotroph tumors, the data on correlates of tumor granulation patterns in functional TPIT lineage pituitary neuroendocrine tumors (corticotroph tumors) have been less uniformly documented in most clinical series. This study evaluated characteristics of 41 well-characterized functional corticotroph tumors consisting of 28 densely granulated corticotroph tumors (DGCTs) and 13 sparsely granulated corticotroph tumors (SGCTs) with respect to preoperative clinical and radiological findings, tumor proliferative activity (including mitotic count and Ki-67 labeling index), and postoperative early biochemical remission rates. The median (interquartile range (IQR)) tumor size was significantly larger in the SGCT group [16.00 (16.00) mm in SGCT vs 8.5 (9.75) mm in DGCT, p = 0.049]. T2-weighted signal intensity and T2 intensity (quantitative) did not yield statistical significance based on tumor granulation; however, the T2 intensity-to-white matter ratio was significantly higher in SGCTs (p = 0.049). The median (IQR) Ki-67 labeling index was 2.00% (IQR 1.00%) in the DGCT group and 4.00% (IQR 7.00%) in the SGCT group (p = 0.043). The mitotic count per 2 mm2 was higher in the SGCT group (p = 0.001). In the multivariate analysis, the sparse granulation pattern (SGCT) remained an independent predictor of a lower probability of early biochemical remission irrespective of the tumor size and proliferative activity (p = 0.012). The current study further supports the impact of tumor granulation pattern as a biologic variable and warrants the detailed histological subtyping of functional corticotroph tumors as indicated in the WHO classification of pituitary neuroendocrine tumors. More importantly, the assessment of the quantitative T2 intensity-to-white matter ratio may serve as a preoperative radiological harbinger of SGCTs.

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来源期刊
Endocrine Pathology
Endocrine Pathology 医学-病理学
CiteScore
12.30
自引率
20.50%
发文量
41
审稿时长
>12 weeks
期刊介绍: Endocrine Pathology publishes original articles on clinical and basic aspects of endocrine disorders. Work with animals or in vitro techniques is acceptable if it is relevant to human normal or abnormal endocrinology. Manuscripts will be considered for publication in the form of original articles, case reports, clinical case presentations, reviews, and descriptions of techniques. Submission of a paper implies that it reports unpublished work, except in abstract form, and is not being submitted simultaneously to another publication. Accepted manuscripts become the sole property of Endocrine Pathology and may not be published elsewhere without written consent from the publisher. All articles are subject to review by experienced referees. The Editors and Editorial Board judge manuscripts suitable for publication, and decisions by the Editors are final.
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