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Correlation Between Aspirin Intake and Reduced Growth of Human Vestibular Schwannoma: Volumetric Analysis.阿司匹林摄入与人类前庭神经鞘瘤生长减缓之间的相关性:体积分析
Otol Neurotol. 2016 Oct;37(9):1428-34. doi: 10.1097/MAO.0000000000001180.
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Volumetric analysis of tumor control following subtotal and near-total resection of vestibular schwannoma.前庭神经鞘瘤次全切除和近全切除术后肿瘤控制的容积分析。
Laryngoscope. 2016 Aug;126(8):1877-82. doi: 10.1002/lary.25779. Epub 2015 Nov 24.
3
Microsurgical management of vestibular schwannoma after failed previous surgery.前庭神经鞘瘤初次手术后复发的显微外科治疗。
J Neurosurg. 2016 Nov;125(5):1198-1203. doi: 10.3171/2015.8.JNS151350. Epub 2016 Jan 15.
4
Facial Nerve Outcome and Tumor Control Rate as a Function of Degree of Resection in Treatment of Large Acoustic Neuromas: Preliminary Report of the Acoustic Neuroma Subtotal Resection Study (ANSRS).大型听神经瘤治疗中面神经预后和肿瘤控制率与切除程度的关系:听神经瘤次全切除研究(ANSRS)初步报告
Neurosurgery. 2016 Aug;79(2):194-203. doi: 10.1227/NEU.0000000000001162.
5
Functional Preservation After Planned Partial Resection Followed by Gamma Knife Radiosurgery for Large Vestibular Schwannomas.大型前庭神经鞘瘤计划行部分切除术后联合伽玛刀放射外科治疗后的功能保留
World Neurosurg. 2015 Aug;84(2):292-300. doi: 10.1016/j.wneu.2015.03.012. Epub 2015 Mar 16.
6
Nonsteroidal anti-inflammatory medications are cytostatic against human vestibular schwannomas.非甾体抗炎药对人前庭神经鞘瘤具有细胞抑制作用。
Transl Res. 2015 Jul;166(1):1-11. doi: 10.1016/j.trsl.2014.12.007. Epub 2015 Jan 7.
7
Aspirin intake correlates with halted growth of sporadic vestibular schwannoma in vivo.阿司匹林摄入与散发性前庭神经鞘瘤体内生长停止相关。
Otol Neurotol. 2014 Feb;35(2):353-7. doi: 10.1097/MAO.0000000000000189.
8
Vestibular schwannoma microsurgery for recurrent tumors after radiation therapy or previous surgical resection.听神经鞘瘤经放射治疗或先前手术切除后复发的显微手术治疗。
Otol Neurotol. 2014 Jan;35(1):171-81. doi: 10.1097/MAO.0000000000000174.
9
Tumor-associated macrophages are related to volumetric growth of vestibular schwannomas.肿瘤相关巨噬细胞与前庭神经鞘瘤的体积增长有关。
Otol Neurotol. 2013 Feb;34(2):347-52. doi: 10.1097/MAO.0b013e31827c9fbf.
10
Intratumoral hemorrhage, vessel density, and the inflammatory reaction contribute to volume increase of sporadic vestibular schwannomas.肿瘤内出血、血管密度和炎症反应导致散发性前庭神经鞘瘤体积增大。
Virchows Arch. 2012 Jun;460(6):629-36. doi: 10.1007/s00428-012-1236-9. Epub 2012 May 4.

巨噬细胞密度可预测前庭神经鞘瘤次全切除术后的面神经预后和肿瘤生长。

Macrophage Density Predicts Facial Nerve Outcome and Tumor Growth after Subtotal Resection of Vestibular Schwannoma.

作者信息

Graffeo Christopher S, Perry Avital, Raghunathan Aditya, Kroneman Trynda N, Jentoft Mark, Driscoll Colin L, Neff Brian A, Carlson Matthew L, Jacob Jeffrey, Link Michael J, Van Gompel Jamie J

机构信息

Department of Neurologic Surgery, Mayo Clinic, Rochester, Minnesota, United States.

Department of Laboratory Medicine & Pathology, Mayo Clinic, Rochester, Minnesota, United States.

出版信息

J Neurol Surg B Skull Base. 2018 Oct;79(5):482-488. doi: 10.1055/s-0038-1627474. Epub 2018 Feb 7.

DOI:10.1055/s-0038-1627474
PMID:30210976
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6133670/
Abstract

Vestibular schwannoma (VS) behavior following subtotal resection (STR) is highly variable. Overall progression rates have been reported as high as 44%, and optimal treatment is controversial. Correspondingly, identification of a reliable clinical or pathologic marker associated with progression after STR would help guide decision-making.  A prospectively maintained institutional VS registry from 1999 to 2014 was retrospectively reviewed for sporadic VS patients who underwent primary STR without preceding stereotactic radiosurgery (SRS) by a single neurosurgery-neurotology team. Primary endpoints included tumor progression and postoperative facial nerve function. Pathologic specimens were stained for Ki67, CD68, S100, and SOX10 and were quantitated by digital imaging analysis. was defined as the ratio of CD68 macrophages to S100 macrophages and Schwannian tumor cells. Clinical outcomes were correlated with pathologic markers.  Forty-six patients met the study inclusion criteria. Thirteen (28%) progressed during a mean 57 months of follow-up (range 15-149). Favorable postoperative facial nerve function (House-Brackmann I-II) was achieved in 37 (80%). CD68 cells were present at significantly higher concentrations in tumors that progressed (  = 0.03). Higher was significantly associated with both tumor progression (  = 0.02) and unfavorable facial nerve function (  = 0.02). Ki67 percent positivity was not significantly associated with either primary endpoint (  = 0.83;  = 0.58).   may provide an important marker for individuals at the highest risk for progression of VS after STR, potentially prompting closer surveillance or consideration for upfront SRS following STR. This finding supports preceding conclusions that an intratumoral macrophage-predominant inflammatory response may be a marker for tumor growth and a potential therapeutic target.

摘要

次全切除(STR)后前庭神经鞘瘤(VS)的行为具有高度变异性。据报道,总体进展率高达44%,最佳治疗方法存在争议。相应地,识别与STR后进展相关的可靠临床或病理标志物将有助于指导决策。 对1999年至2014年前瞻性维护的机构VS登记册进行回顾性研究,纳入由单一神经外科 - 神经耳科学团队进行初次STR且未先行立体定向放射外科手术(SRS)的散发性VS患者。主要终点包括肿瘤进展和术后面神经功能。病理标本进行Ki67、CD68、S100和SOX10染色,并通过数字成像分析进行定量。 定义为CD68巨噬细胞与S100巨噬细胞及施万细胞瘤细胞的比例。临床结果与病理标志物相关。 46例患者符合研究纳入标准。在平均57个月的随访期间(范围15 - 149个月),13例(28%)出现进展。37例(80%)术后面神经功能良好(House - Brackmann I - II级)。进展的肿瘤中CD68细胞浓度显著更高( = 0.03)。较高的 与肿瘤进展( = 0.02)和不良面神经功能( = 0.02)均显著相关。Ki67阳性百分比与两个主要终点均无显著相关性( = 0.83; = 0.58)。   可能为STR后VS进展风险最高的个体提供一个重要标志物,可能促使在STR后进行更密切的监测或考虑先行SRS。这一发现支持了之前的结论,即肿瘤内以巨噬细胞为主的炎症反应可能是肿瘤生长的标志物和潜在的治疗靶点。