Gaudin P B, Sherman M E, Brat D J, Zahurak M, Erozan Y S
Department of Pathology, Johns Hopkins Hospital, Baltimore, MD 21287-6940, USA.
Diagn Cytopathol. 1997 Dec;17(6):461-6. doi: 10.1002/(sici)1097-0339(199712)17:6<461::aid-dc16>3.0.co;2-k.
The accuracy of using a combination of cytopathologic and histopathologic techniques to diagnose stereotactically guided brain biopsies was investigated in 74 patients. Diagnostic accuracy was assessed by determining whether classification of the biopsies as gliosis, astrocytoma (A), anaplastic astrocytoma (AA), or glioblastoma multiforme (GBM) predicted survival. The utility of on-site evaluation using Diff-Quik-stained crush preparations was also assessed. The patients ranged in age from 5 to 88 years (mean, 55 years) and were followed for over 2 years in most cases. Four cases (5%) were classified as gliosis (G), 7 (9%) as atypical gliosis (AG), 4 (5%) as high-grade mixed oligodendroglioma/astrocytoma (OA), 11 (15%) as astrocytoma (A), 21 (28%) as anaplastic astrocytoma (AA), and 27 (36%) as glioblastoma multiforme (GBM). Median survival was 11 months in patient with OA, 57 months in patients with A, 10 months in patients with AA, and 5 months in patients with GBM. Diagnosis of Diff-Quik-stained crush preparations made during the biopsy procedure was highly correlated with the final diagnosis and survival. We conclude that the diagnosis of stereotactic brain biopsies using cytopathology with on-site evaluation in combination with histopathological evaluation of needle cores is accurate based on a survival analysis. However, A and G may be difficult to distinguish.
对74例患者进行了研究,以探讨采用细胞病理学和组织病理学技术相结合的方法诊断立体定向脑活检的准确性。通过确定将活检分类为胶质增生、星形细胞瘤(A)、间变性星形细胞瘤(AA)或多形性胶质母细胞瘤(GBM)是否能预测生存情况来评估诊断准确性。还评估了使用Diff-Quik染色压片标本进行现场评估的效用。患者年龄在5至88岁之间(平均55岁),大多数病例随访超过2年。4例(5%)被分类为胶质增生(G),7例(9%)为非典型胶质增生(AG),4例(5%)为高级别混合性少突胶质细胞瘤/星形细胞瘤(OA),11例(15%)为星形细胞瘤(A),21例(28%)为间变性星形细胞瘤(AA),27例(36%)为多形性胶质母细胞瘤(GBM)。OA患者的中位生存期为11个月,A患者为57个月,AA患者为10个月,GBM患者为5个月。活检过程中制作的Diff-Quik染色压片标本的诊断与最终诊断及生存情况高度相关。我们得出结论,基于生存分析,采用细胞病理学结合现场评估以及针芯组织病理学评估来诊断立体定向脑活检是准确的。然而,A和G可能难以区分。