Xu Ran, Rösler Judith, Teich Wanda, Radke Josefine, Früh Anton, Scherschinski Lea, Onken Julia, Vajkoczy Peter, Misch Martin, Faust Katharina
Department of Neurosurgery, Charité-Universitätsmedizin Berlin, Corporate Member of Freie Universität Berlin, and Humboldt-Universität zu Berlin, and Berlin Institute of Health, 13353 Berlin, Germany.
BIH Charité (Junior) (Digital) Clinician Scientist Program, Berlin Institute of Health at Charité-Universitätsmedizin Berlin, BIH Biomedical Innovation Academy, Charitéplatz 1, 10117 Berlin, Germany.
J Clin Med. 2022 Jun 10;11(12):3330. doi: 10.3390/jcm11123330.
The utilization of fluorescein-guided biopsies has recently been discussed to improve and expedite operative techniques in the detection of tumor-positive tissue, as well as to avoid making sampling errors. In this study, we aimed to report our experience with fluorescein-guided biopsies and elucidate distribution patterns in different histopathological diagnoses in order to develop strategies to increase the efficiency and accuracy of this technique. We report on 45 fluorescence-guided stereotactic biopsies in 44 patients (15 female, 29 male) at our institution from March 2016 to March 2021, including 25 frame-based stereotactic biopsies and 20 frameless image-guided biopsies using VarioGuide. A total number of 347 biopsy samples with a median of 8 samples (range: 4-18) per patient were evaluated for intraoperative fluorescein uptake and correlated to definitive histopathology. The median age at surgery was 63 years (range: 18-87). Of the acquired specimens, 63% were fluorescein positive. Final histopathology included glioblastoma (n = 16), B-cell non-Hodgkin lymphoma (n = 10), astrocytoma, IDH-mutant WHO grade III (n = 6), astrocytoma, IDH-mutant WHO grade II (n = 1), oligodendroglioma, IDH-mutant and 1p/19q-codeleted WHO grade II (n = 2), reactive CNS tissue/inflammation (n = 4), post-transplantation lymphoproliferative disorder (PTLD; n = 2), ependymoma (n = 1), infection (toxoplasmosis; n = 1), multiple sclerosis (n = 1), and metastasis (n = 1). The sensitivity for high-grade gliomas was 85%, and the specificity was 70%. For contrast-enhancing lesions, the specificity of fluorescein was 84%. The number needed to sample for contrast-enhancing lesions was three, and the overall number needed to sample for final histopathological diagnosis was five. Interestingly, in the astrocytoma, IDH-mutant WHO grade III group, 22/46 (48%) demonstrated fluorescein uptake despite no evidence for gadolinium uptake, and 73% of these were tumor-positive. In our patient series, fluorescein-guided stereotactic biopsy increases the likelihood of definitive neuropathological diagnosis, and the number needed to sample can be reduced by 50% in contrast-enhancing lesions.
最近,人们讨论了利用荧光素引导活检来改进和加快肿瘤阳性组织检测中的手术技术,并避免出现采样误差。在本研究中,我们旨在报告我们在荧光素引导活检方面的经验,并阐明不同组织病理学诊断中的分布模式,以便制定提高该技术效率和准确性的策略。我们报告了2016年3月至2021年3月期间在我们机构对44例患者(15名女性,29名男性)进行的45次荧光引导立体定向活检,包括25次基于框架的立体定向活检和20次使用VarioGuide的无框架图像引导活检。对总共347个活检样本(每位患者中位数为8个样本,范围:4 - 18个)进行术中荧光素摄取评估,并与最终组织病理学结果相关联。手术时的中位年龄为63岁(范围:18 - 87岁)。在获取的标本中,63%为荧光素阳性。最终组织病理学结果包括胶质母细胞瘤(n = 16)、B细胞非霍奇金淋巴瘤(n = 10)、异柠檬酸脱氢酶(IDH)突变的WHO III级星形细胞瘤(n = 6)、IDH突变的WHO II级星形细胞瘤(n = 1)、IDH突变且1p/19q共缺失的WHO II级少突胶质细胞瘤(n = 2)、反应性中枢神经系统组织/炎症(n = 4)、移植后淋巴细胞增殖性疾病(PTLD;n = 2)、室管膜瘤(n = 1)、感染(弓形虫病;n = 1)、多发性硬化症(n = 1)和转移瘤(n = 1)。高级别胶质瘤的敏感性为85%,特异性为70%。对于强化病变,荧光素的特异性为84%。强化病变的采样数量为3个,最终组织病理学诊断的总体采样数量为5个。有趣的是,在IDH突变的WHO III级星形细胞瘤组中,22/46(48%)尽管没有钆摄取的证据,但显示有荧光素摄取,其中73%为肿瘤阳性。在我们的患者系列中,荧光素引导立体定向活检增加了明确神经病理学诊断的可能性,对于强化病变,采样数量可减少50%。