Kim S E, Cho J T, Lee D S, Chung J K, Kim S, Lee M C, Lee J S, Koh C S
Department of Nuclear Medicine and Internal Medicine, Seoul National University College of Medicine, Korea.
J Korean Med Sci. 1994 Feb;9(1):29-34. doi: 10.3346/jkms.1994.9.1.29.
We present a patient with Fanconi syndrome who demonstrated poor renal uptake of 99mTc-DMSA and high urinary concentration of the tracer. A 99mTc-DTPA scan was normal and the creatinine clearance only minimally decreased. These findings suggest that 99mTc-DMSA may be accumulated in the kidney by glomerular filtration and subsequent tubular reabsorption, with the nonabsorbed fraction appearing in the urine. In Fanconi Syndrome the tubular reabsorption of DMSA may also be reduced, thus explaining the poor renal uptake in this patient. A 99mTc-MDP bone scan showed faint renal uptake and diffuse high uptake mainly in the spine, demonstrating that the metabolic bone disease associated with Fanconi Syndrome can be another mechanism for poor renal visualization on bone scan.
我们报告一名患有范科尼综合征的患者,其表现为肾脏对99mTc-DMSA摄取不佳且示踪剂在尿液中的浓度较高。99mTc-DTPA扫描正常,肌酐清除率仅略有下降。这些发现表明,99mTc-DMSA可能通过肾小球滤过及随后的肾小管重吸收在肾脏中蓄积,未被吸收的部分则出现在尿液中。在范科尼综合征中,DMSA的肾小管重吸收也可能减少,这就解释了该患者肾脏摄取不佳的原因。99mTc-MDP骨扫描显示肾脏摄取微弱,主要在脊柱出现弥漫性高摄取,表明与范科尼综合征相关的代谢性骨病可能是骨扫描时肾脏显影不佳的另一种机制。