Department of Radiology, Korea University Ansan Hospital, Kyunggi-do, Korea.
AJNR Am J Neuroradiol. 2010 Mar;31(3):498-503. doi: 10.3174/ajnr.A1864. Epub 2009 Oct 29.
Most intramedullary astrocytomas have been known to exhibit at least some enhancement on MR imaging regardless of cell type or tumor grade. The purpose of this study was to evaluate the incidence of nonenhancing intramedullary astrocytomas through a retrospective study within our institutions and a systematic review of the medical literature.
A total of 19 consecutive patients (male to female ratio, 11:8; mean age, 27.84 +/- 19.0 years) with primary intramedullary astrocytomas (3 WHO grade I, 13 WHO grade II, 3 WHO grade III) who underwent preoperative MR imaging with contrast enhancement were included in this retrospective study from 4 institutions. The tumor-enhancement patterns were classified into the following categories: 1) no enhancement, 2) focal nodular enhancement, 3) patchy enhancement, 4) inhomogeneous diffuse enhancement, and 5) homogeneous diffuse enhancement. Seven articles including MR imaging enhancement studies of intramedullary astrocytomas were eligible for literature review.
In the retrospective study, 6 astrocytomas (32%), including 2 anaplastic astrocytomas, did not enhance at all. Focal nodular enhancement was identified in 5 astrocytomas (26%); patchy enhancement, in 3 (16%); inhomogeneous diffuse enhancement, in 5 (26%); and homogeneous diffuse enhancement, in none. In the literature review, the frequency of nonenhancing intramedullary astrocytomas was 14 of 76 (18%), including 2 anaplastic astrocytomas.
Nonenhancing intramedullary astrocytomas are not uncommon and comprise between 20% and 30% of intramedullary astrocytomas. Therefore, astrocytoma must remain in the differential diagnosis of nonenhancing intramedullary lesions, particularly if the lesion demonstrates a prominent mass effect or cord expansion.
大多数脊髓内星形细胞瘤在磁共振成像(MR)上至少有一定程度的强化,无论细胞类型或肿瘤级别如何。本研究的目的是通过对我们机构内的回顾性研究和对医学文献的系统回顾,评估非增强性脊髓内星形细胞瘤的发生率。
本研究共纳入了 19 例连续的原发性脊髓内星形细胞瘤患者(男/女比例为 11:8;平均年龄为 27.84 ± 19.0 岁),这些患者均在 4 家机构接受了术前 MR 成像增强检查。肿瘤强化模式分为以下几类:1)无强化,2)局灶性结节强化,3)斑片状强化,4)不均匀弥漫性强化,5)均匀弥漫性强化。有 7 篇包括脊髓内星形细胞瘤 MR 成像增强研究的文章符合文献综述的纳入标准。
在回顾性研究中,6 例星形细胞瘤(32%)完全无强化,其中包括 2 例间变性星形细胞瘤。5 例星形细胞瘤表现为局灶性结节强化(26%);3 例表现为斑片状强化(16%);5 例表现为不均匀弥漫性强化(26%);无一例表现为均匀弥漫性强化。在文献综述中,非增强性脊髓内星形细胞瘤的发生率为 76 例中的 14 例(18%),其中包括 2 例间变性星形细胞瘤。
非增强性脊髓内星形细胞瘤并不少见,占脊髓内星形细胞瘤的 20%至 30%。因此,星形细胞瘤必须是无强化性脊髓内病变的鉴别诊断之一,特别是如果病变表现出明显的占位效应或脊髓扩张。