Daldrup-Link Heike E, Rummeny Ernst J, Ihssen Bettina, Kienast Joachim, Link Thomas M
Department of Radiology, Technical University of Munich, Ismaninger Strasse 22, 81675 Munich, Germany.
Eur Radiol. 2002 Jun;12(6):1557-66. doi: 10.1007/s00330-001-1270-5. Epub 2002 Feb 5.
The aim of this study was to differentiate normal, hypercellular, and neoplastic bone marrow based on its MR enhancement after intravenous administration of superparamagnetic iron oxides in patients with cancer of the hematopoietic system. Eighteen patients with cancer of the hematopoietic system underwent MRI of the spine before and after infusion of ferumoxides ( n=9) and ferumoxtran ( n=9) using T1- and T2-weighted turbo spin-echo (TSE) and short tau inversion recovery sequences (STIR). In all patients diffuse or multifocal bone marrow infiltration was suspected, based on iliac crest biopsy and imaging such as conventional radiographs, MRI, and positron emission tomography. In addition, all patients had a therapy-induced normocellular ( n=7) or hypercellular ( n=11) reconversion of the normal non-neoplastic bone marrow. The MRI data were analyzed by measuring pre- and post-contrast signal intensities (SI) of hematopoietic and neoplastic marrow and by calculating the enhancement as deltaSI(%) data and the tumor-to-bone-marrow contrast as contrast-to-noise ratios (CNR). Changes in bone marrow signal intensity after iron oxide administration were more pronounced on STIR images as compared with T1- and T2-weighted TSE images. The STIR images showed a strong signal decline of normal and hypercellular marrow 45-60 min after iron oxide infusion, but no or only a minor signal decline of neoplastic bone marrow lesions; thus, deltaSI% data were significantly higher in normal and hypercellular reconverted marrow compared with neoplastic bone marrow lesions ( p<0.05). Additionally, the contrast between focal or multifocal neoplastic bone marrow infiltration and normal bone marrow, quantified by CNR data, increased significantly on post-contrast STIR images compared with precontrast images ( p<0.05). Superparamagnetic iron oxides are taken up by normal and hypercellular reconverted bone marrow, but not by neoplastic bone marrow lesions, thereby providing significantly different enhancement patterns on T2-weighted MR images; thus, superparamagnetic iron oxides are useful to differentiate normal and neoplastic bone marrow and to increase the bone marrow-to-tumor contrast.
本研究的目的是,基于静脉注射超顺磁性氧化铁后骨髓的磁共振增强情况,对造血系统癌症患者的正常、细胞增多和肿瘤性骨髓进行鉴别。18例造血系统癌症患者在输注菲立磁(n = 9)和 ferumoxtran(n = 9)前后,使用T1加权和T2加权快速自旋回波(TSE)序列以及短tau反转恢复序列(STIR)进行了脊柱MRI检查。根据髂嵴活检以及传统X线片、MRI和正电子发射断层扫描等影像学检查,所有患者均怀疑存在弥漫性或多灶性骨髓浸润。此外,所有患者的正常非肿瘤性骨髓均出现了治疗诱导的正常细胞(n = 7)或细胞增多(n = 11)再转换。通过测量造血和肿瘤性骨髓对比剂注射前后的信号强度(SI),并计算增强率作为deltaSI(%)数据以及肿瘤与骨髓的对比度作为对比噪声比(CNR),对MRI数据进行分析。与T1加权和T2加权TSE图像相比,氧化铁给药后骨髓信号强度的变化在STIR图像上更为明显。STIR图像显示,氧化铁输注后45 - 60分钟,正常和细胞增多的骨髓信号强烈下降,但肿瘤性骨髓病变无信号下降或仅有轻微信号下降;因此,正常和细胞增多再转换骨髓的deltaSI%数据显著高于肿瘤性骨髓病变(p < 0.05)。此外,与对比前图像相比,通过CNR数据量化的局灶性或多灶性肿瘤性骨髓浸润与正常骨髓之间的对比度在对比后STIR图像上显著增加(p < 0.05)。超顺磁性氧化铁被正常和细胞增多再转换的骨髓摄取,但不被肿瘤性骨髓病变摄取,从而在T2加权MR图像上提供显著不同的增强模式;因此,超顺磁性氧化铁有助于鉴别正常和肿瘤性骨髓,并增加骨髓与肿瘤的对比度。