Staffen W, Hondl N, Trinka E, Iglseder B, Unterrainer J, Ladurner G
Department of Neurology, Landesnervenklinik Salzburg, Austria.
Nucl Med Commun. 1998 Apr;19(4):335-40. doi: 10.1097/00006231-199804000-00007.
Magnetic resonance imaging (MRI) and computed tomography (CT) may not be reliable in the differential diagnosis of tumour necrosis, scar and recurrent tumour. We compared 201Tl-chloride SPET with CT and MRI for the differential diagnosis of these cerebral lesions. Brain SPET was performed in 40 patients after the intravenous injection of 201Tl-chloride. All 40 patients also had a CT or MRI scan, and a histological diagnosis was available for 27 of the patients. For each patient, the ratio of counts in the lesion region of interest (ROI) to counts in the contralateral ROI was calculated and found to be between 0.58 and 9.60. The ratios for high-grade gliomas, metastases and meningiomas were high (> 2.7), especially in tumours with good vascularization. A low ratio (< 1.7) was noted in patients with low-grade astrocytoma, necrosis or ischaemic lesions. There were two exceptional cases of ischaemic lesions in the luxury perfusion stage (ratios of 3.61 and 3.87), as verified by HMPAO-SPET. We found that 201Tl-chloride SPET helps to differentiate between malignant tumours, poorly vascularized benign lesions and necrosis. Differentiation between low-grade astrocytoma and non-malignant lesions was not possible, but there was a trend towards differentiating between low-grade astrocytoma and ischaemic infarction. The timing of the investigation is important to avoid false-positive results in hyperperfused ischaemic tissue.
磁共振成像(MRI)和计算机断层扫描(CT)在肿瘤坏死、瘢痕和肿瘤复发的鉴别诊断中可能并不可靠。我们比较了氯化铊201单光子发射计算机断层显像(201Tl-chloride SPET)与CT和MRI对这些脑病变的鉴别诊断。40例患者在静脉注射氯化铊201后进行了脑SPET检查。所有40例患者均进行了CT或MRI扫描,其中27例患者有组织学诊断结果。对每位患者,计算病变感兴趣区(ROI)与对侧ROI的计数比值,发现该比值在0.58至9.60之间。高级别胶质瘤、转移瘤和脑膜瘤的比值较高(>2.7),尤其是在血管化良好的肿瘤中。低级别星形细胞瘤、坏死或缺血性病变患者的比值较低(<1.7)。有两例处于过度灌注期的缺血性病变例外情况(比值分别为3.61和3.87),经锝-99m六甲基丙烯胺肟单光子发射计算机断层显像(HMPAO-SPET)证实。我们发现氯化铊201 SPET有助于鉴别恶性肿瘤、血管化不良的良性病变和坏死。无法区分低级别星形细胞瘤与非恶性病变,但有区分低级别星形细胞瘤和缺血性梗死的趋势。检查时机很重要,以避免在过度灌注的缺血组织中出现假阳性结果。