Literature DB >> 9884419

Poor renal accumulation of 99mTc-DMSA in idiopathic tubular proteinuria.

S Suzuki1, J Suzuki, K Kume, K Yoshida, H Suyama, Y Kawasaki, R Nozawa, H Suzuki, T Fujiki, S Kamiyama, A Suzuki.   

Abstract

In Japanese patients idiopathic tubular proteinuria presents mainly as asymptomatic tubular low molecular weight proteinuria. This disease has recently been shown to resemble Dent's disease which is characterized by tubular proteinuria, hypercalciuria, rickets and eventual renal failure. We report on 4 children with idiopathic tubular proteinuria. Although they had normal renal function, as evidenced by serum creatinine or creatinine clearance, they had very poor renal accumulation of 99mTc-DMSA and the presence of large amounts of tracer in the bladder. Additionally, the patient with the largest amounts of tubular proteinuria had the poorest renal accumulation of the 4 patients. The renal accumulation of tracer decreased with time from a maximum at 10 min after injection. These findings demonstrate that the tracer, once taken to be confined to the proximal tubular cells, is immediately excreted to the tubular lumen. We suggest that poor renal accumulation of 99mTc-DMSA is very important in elucidating the mechanism of idiopathic tubular proteinuria, and that 99mTc-DMSA renoscintigraphy is useful in the evaluation of the patient's renal function over time.

Entities:  

Mesh:

Substances:

Year:  1999        PMID: 9884419     DOI: 10.1159/000045245

Source DB:  PubMed          Journal:  Nephron        ISSN: 1660-8151            Impact factor:   2.847


  7 in total

1.  An unusual DMSA scan: answer.

Authors:  Alison Timmis; Caroline Jones; Fauzia Paize
Journal:  Pediatr Nephrol       Date:  2011-06-08       Impact factor: 3.714

Review 2.  Novel techniques and newer markers for the evaluation of "proximal tubular dysfunction".

Authors:  Michael Ludwig; Sidharth K Sethi
Journal:  Int Urol Nephrol       Date:  2011-03-01       Impact factor: 2.370

3.  Clinical and laboratory features of Macedonian children with OCRL mutations.

Authors:  Velibor Tasic; Vladimir J Lozanovski; Petar Korneti; Nadica Ristoska-Bojkovska; Vesna Sabolic-Avramovska; Zoran Gucev; Michael Ludwig
Journal:  Pediatr Nephrol       Date:  2011-01-20       Impact factor: 3.714

Review 4.  Hereditary causes of kidney stones and chronic kidney disease.

Authors:  Vidar O Edvardsson; David S Goldfarb; John C Lieske; Lada Beara-Lasic; Franca Anglani; Dawn S Milliner; Runolfur Palsson
Journal:  Pediatr Nephrol       Date:  2013-01-20       Impact factor: 3.714

5.  Decreased renal uptake of (99m)Tc-DMSA in patients with tubular proteinuria.

Authors:  Beom Hee Lee; So Hee Lee; Hyun Jin Choi; Hee Gyung Kang; So Won Oh; Dong Soo Lee; Il Soo Ha; Yong Choi; Hae Il Cheong
Journal:  Pediatr Nephrol       Date:  2009-07-05       Impact factor: 3.714

6.  Dent's disease manifesting as focal glomerulosclerosis: Is it the tip of the iceberg?

Authors:  Yaacov Frishberg; Dganit Dinour; Ruth Belostotsky; Rachel Becker-Cohen; Choni Rinat; Sofia Feinstein; Paulina Navon-Elkan; Efrat Ben-Shalom
Journal:  Pediatr Nephrol       Date:  2009-12       Impact factor: 3.714

Review 7.  The oculocerebrorenal syndrome of Lowe: an update.

Authors:  Arend Bökenkamp; Michael Ludwig
Journal:  Pediatr Nephrol       Date:  2016-03-24       Impact factor: 3.714

  7 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.