Magnetic Resonance Imaging Evaluation of Common Spinal Intramedullary Tumours: Ependymoma and Astrocytoma.

Mymensingh medical journal : MMJ Pub Date : 2023-07-01
N Sultana, S Jabeen, S Rima, U K Nag, S K Sarkar
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Abstract

This cross-sectional study was carried out in the Department of Radiology and Imaging, Bangabandhu Sheikh Mujib Medical University (BSMMU), Dhaka, Bangladesh, from January 2015 to June 2016 in collaboration with Department of Neurosurgery and Department of Pathology of same hospital, to assess MRI findings of common IMSCTs and to find out the validity of MRI in the diagnosis of spinal ependymoma and astrocytoma, thereby differentiating these two common intramedullary entities. For this purpose, 40 patients aged from 15 to 60 years, who were diagnosed or suspected cases of having intramedullary spinal cord tumours were enrolled. These patients underwent preoperative MRI for evaluation of the spinal cord tumours during the study period in department of Radiology and Imaging. Also, patients were diagnosed by MRI as having IMSCTs incidentally was included. All of them were followed by histopathological examination of the same lesions after surgery. Among these 40 patients after exclusion for valid reason 28 cases were included as study population. MR images were obtained on a 1.5 Tesla (Avanto Magnatom, Siemens) unit with a spine surface coil. MRI findings were compared with histopathology after surgery keeping histopathology as gold standard. Out of 28 clinically and MRI diagnosed IMSCTs cases, 19 cases of ependymoma, 8 cases of astrocytoma and one diagnosed as hemangioblastoma by MRI. The mean age was 34.11±9.55 years, ranging from 15 to 56 years for ependymoma, 26.88±8.08 years ranging from 16 to 44 years for astrocytoma. Highest incidence (47.4%) was in between 31 to 40 years for ependymoma, 50.0% were in between 21-30 for Astrocytoma. On MRI majority 12(63.2%) of the cord ependymomas and majority 5(62.5%) of astrocytomas were in cervical region. While considering axial location ependymomas are mostly 17(89.5%) central and astrocytomas 5(62.5%) are eccentric in location. It was observed that out of 19 cases of ependymoma more than half 10(52.6%) had elongated shape, 12(63.1%) had well defined margin. Associated syringohydromyelia was present in 16(84.2%) cases. On T1WI 11(57.9%) and 8(42.1%) cases were iso and hypo respectively. On T2WI 14(73.7%) cases were hyper intense. After Gd-DTPA in most cases, 13(68.4%) cases showed diffuse enhancement. Noticeable and sizeable solid component observed among 13(68.4%) of the cases. Hemorrhage with cap sign was found in more than one third 7(36.8%) cases. Out of 8 cases of astrocytomas 4(50.0%) had lobulated shape, ill-defined margin 5(62.5%). T1WI: Iso 5(62.5%), hypo 3(37.5%), T2WI: hyper 5(62.5%), After Gd-DTPA: focal and heterogenous enhancement 3(37.5%) and rim enhancement 4(50.0%). Component: mixed 4(50.0%), cystic 3(37.5%) and solid 1(12.5%). Hemorrhage without cap sign 2(25.0%), associated syringohydromyelia 1(12.5%). In the case of evaluation of intramedullary ependymoma sensitivity of MRI in the present series is 94.44%, specificity 80.0%, Positive predictive value (PPV) 89.5%, Negative predictive value (NPV) 88.9% and accuracy 89.28%. In case of MRI evaluation of intramedullary astrocytoma sensitivity of MRI in the present study is 85.71%, specificity 90.47%, PPV 75%, NPV 95% and accuracy 89.2%. Thus present study shows MRI is a sensitive and effective noninvasive imaging modality in diagnosing common intramedullary spinal cord tumours.

常见脊髓髓内肿瘤:室管膜瘤和星形细胞瘤的磁共振成像评价。
本横断面研究于2015年1月至2016年6月在孟加拉国达卡班班杜谢赫穆吉布医科大学(BSMMU)放射与影像科与该院神经外科、病理科合作开展,评估常见IMSCTs的MRI表现,探讨MRI诊断脊髓室管膜瘤和星形细胞瘤的有效性,从而鉴别这两种常见的髓内实体。为此,研究人员招募了40名年龄在15至60岁之间、被诊断或疑似患有髓内脊髓肿瘤的患者。这些患者在研究期间在放射与影像科接受术前MRI评估脊髓肿瘤。此外,通过MRI诊断的患者顺便包括了imsct。所有患者术后均对同一病灶进行组织病理学检查。经合理排除的40例患者中有28例纳入研究人群。在带有脊柱表面线圈的1.5 Tesla (Avanto Magnatom, Siemens)设备上获得MR图像。术后以组织病理学为金标准,与MRI检查结果进行比较。在28例临床及MRI诊断的IMSCTs病例中,19例室管膜瘤,8例星形细胞瘤,1例MRI诊断为血管母细胞瘤。平均年龄34.11±9.55岁,室管膜瘤15 ~ 56岁,星形细胞瘤16 ~ 44岁,26.88±8.08岁。室管膜瘤31 ~ 40岁发生率最高(47.4%),星形细胞瘤21 ~ 30岁发生率最高(50.0%)。MRI显示,脊髓室管膜瘤12例(63.2%),星形细胞瘤5例(62.5%)位于宫颈。考虑轴位时,室管膜瘤17例(89.5%)位于中心,星形细胞瘤5例(62.5%)位于偏心位置。我们观察到在19例室管膜瘤中,超过半数(52.6%)呈细长状,12例(63.1%)边缘清晰。16例(84.2%)合并脊髓灰质炎。T1WI呈阳性11例(57.9%),阴性8例(42.1%)。T2WI高强度14例(73.7%)。多数Gd-DTPA后,13例(68.4%)呈弥漫性强化。13例(68.4%)观察到明显且较大的实性成分。出血伴帽征者超过1 / 3(36.8%)。8例星形细胞瘤中4例(50.0%)呈分叶状,边缘不清5例(62.5%)。T1WI: Iso 5(62.5%),低3(37.5%),T2WI:高5(62.5%),Gd-DTPA后:局灶和异质增强3(37.5%)和边缘增强4(50.0%)。成分:混合型4(50.0%),囊性3(37.5%),实性1(12.5%)。无帽征2型出血(25.0%),伴脊髓水肿1型(12.5%)。本系列MRI对髓内室管膜瘤的敏感性为94.44%,特异性为80.0%,阳性预测值(PPV)为89.5%,阴性预测值(NPV)为88.9%,准确率为89.28%。本研究MRI对髓内星形细胞瘤的敏感性为85.71%,特异性为90.47%,PPV为75%,NPV为95%,准确率为89.2%。因此,本研究表明MRI是诊断常见脊髓髓内肿瘤的一种灵敏、有效的无创成像方式。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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