Nishimura R, Takahashi M, Morishita S, Sumi M, Uozumi H, Sakamoto Y
Department of Radiology, Kumamoto University School of Medicine, Japan.
Radiat Med. 1992 May-Jun;10(3):109-16.
MR examinations of 104 patients who had undergone radiotherapy to the brain were reviewed. Thirty-six patients received Gd-DTPA enhanced study during the course of MR evaluation and six of the patients showed enhancing radiation necrosis. Histopathological confirmations were obtained in three patients. Gd-DTPA enhancing radiation lesions were multiple and patchy in three patients, multiple and patchy with cyst formation in two and ring shaped in one. In terms of their distribution, enhancing lesions in four patients were seen only in the white matter within the irradiated field and these patients had undergone radiotherapy within five years. The interval after radiotherapy was more than eight years in two patients and their enhanced lesions were observed in both the white and gray matter. Histopathological findings of Gd-DTPA enhancing radiation necrosis were gliosis and coalescing vacuoles of the neural tissue. None of these enhanced radiation lesions showed significant mass effects. Patterns of the enhancement were not specific. It was considered to be difficult to differentiate tumor recurrence from radiation necrosis with conventional Gd-DTPA enhanced MR examinations. In one patient, delayed MR images after Gd-DTPA administration showed increases in the size and number of radiation enhanced lesions. Dynamic and delayed MR study might add more information to conventional imaging after Gd-DTPA. Further studies are necessary to differentiate radiation lesions from tumor recurrences.
对104例接受过脑部放疗的患者的磁共振成像(MR)检查进行了回顾。36例患者在MR评估过程中接受了钆喷酸葡胺(Gd-DTPA)增强检查,其中6例显示有放射性坏死增强。3例患者获得了组织病理学证实。Gd-DTPA增强的放射性病变在3例患者中为多发且呈斑片状,2例为多发斑片状伴囊肿形成,1例为环形。就其分布而言,4例患者的增强病变仅见于照射野内的白质,且这些患者在5年内接受了放疗。2例患者放疗后的间隔时间超过8年,其增强病变在白质和灰质中均有观察到。Gd-DTPA增强的放射性坏死的组织病理学表现为神经组织的胶质增生和融合性空泡。这些增强的放射性病变均未显示明显的占位效应。增强模式不具有特异性。认为用传统的Gd-DTPA增强MR检查很难区分肿瘤复发和放射性坏死。在1例患者中,Gd-DTPA给药后的延迟MR图像显示放射性增强病变的大小和数量增加。动态和延迟MR研究可能会为Gd-DTPA后的传统成像增加更多信息。需要进一步研究以区分放射性病变和肿瘤复发。