Reasner C A, Ghiatas A A, Sirinek K R, Yee R W
Department of Medicine/Endocrinology, University of Texas Health Science Center, San Antonio 78284-7877.
South Med J. 1990 Mar;83(3):343-5. doi: 10.1097/00007611-199003000-00023.
Ectopic, epinephrine-secreting pheochromocytomas are rare and difficult to diagnose. In our case, MRI was able to show the lesion, which could not be clearly identified by CT. The histologic specificity provided by T2-weighted images confirmed the biochemical diagnosis of pheochromocytoma. MRI should be considered as an alternative to CT in the diagnosis of familial pheochromocytomas.
异位分泌肾上腺素的嗜铬细胞瘤罕见且难以诊断。在我们的病例中,磁共振成像(MRI)能够显示出该病变,而计算机断层扫描(CT)却无法清晰识别。T2加权图像所提供的组织学特异性证实了嗜铬细胞瘤的生化诊断。在家族性嗜铬细胞瘤的诊断中,应考虑将MRI作为CT的替代检查方法。