Skip to main content
Log in

A rare case of nephrotic syndrome associated with Dent’s disease: a case report

  • Case Report
  • Published:
CEN Case Reports Aims and scope Submit manuscript

Abstract

Dent’s disease is a rare X-linked condition caused by a mutation in CLCN5 and OCRL gene, which impair the megalin-cubilin receptor-mediated endocytosis in kidney’s proximal tubules. Thus, it may manifest as nephrotic-range low-molecular-weight proteinuria (LMWP). On the other hand, glomerular proteinuria, hypoalbuminemia, and edema formation are the key features of nephrotic syndrome that rarely found in Dent’s disease. Here, we reported a man in his 30 s with Dent’s disease presented with leg edema for 5 days. The laboratory results revealed hypoalbuminemia and a decrease of urine β2-microglobulin/urine protein ratio (Uβ2-MG /UP), indicating that the primary origin of proteinuria shifted from LMWP to glomerular proteins. The kidney biopsy revealed glomerular abnormality and calcium deposition in the renal medulla. Electron microscopy of the kidney tissue indicated extensive foot-process effacement of the glomerular podocytes and degeneration of tubular epithelium. After a combination of treatment with prednisolone and cyclosporine (CyA), the nephrotic syndrome was remitted. Given the atypical clinical presentation and the shift of LMWP to glomerular proteinuria in this patient, glomerulopathy and the Dent’s disease existed separately in this patient.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Fig. 1
Fig. 2
Fig. 3
Fig. 4

Similar content being viewed by others

References

  1. van Berkel Y, Ludwig M, van Wijk JAE, Bökenkamp A. Proteinuria in Dent disease: a review of the literature. Pediatr Nephrol. 2017;32(10):1851–9. https://doi.org/10.1007/s00467-016-3499-x.

    Article  PubMed  Google Scholar 

  2. Devuyst O, Thakker RV. Dent’s disease. Orphanet J Rare Desease. 2010;5(28):1–8. https://doi.org/10.1186/1750-1172-5-28.

    Article  Google Scholar 

  3. Peterson PA, Evrin PE, Berggård I. Differentiation of glomerular, tubular, and normal proteinuria: determinations of urinary excretion of beta-2-macroglobulin, albumin, and total protein. J Clin Invest. 1969;48(7):1189–98. https://doi.org/10.1172/JCI106083.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  4. Yu H, Yanagisawa Y, Forbes MA, Cooper EH, Crockson RA, MacLennan IC. Alpha-1-microglobulin: an indicator protein for renal tubular function. J Clin Pathol. 1983;36(3):253–9. https://doi.org/10.1136/jcp.36.3.253.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  5. Bernard AM, Moreau D, Lauwerys R. Comparison of retinol-binding protein and β2-microglobulin determination in urine for the early detection of tubular proteinuria. Clin Chim Acta. 1982;126(1):1–7. https://doi.org/10.1016/0009-8981(82)90356-4.

    Article  CAS  PubMed  Google Scholar 

  6. Wang X, Anglani F, Beara-Lasic L, Mehta AJ, Vaughan LE, Herrera Hernandez L, et al. Glomerular pathology in dent disease and its association with kidney function. Clin J Am Soc Nephrol. 2016;11(12):2168–76. https://doi.org/10.2215/CJN.03710416.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  7. Fervenza FC. A patient with nephrotic-range proteinuria and focal global glomerulosclerosis. Clin J Am Soc Nephrol. 2013;8(11):1979–87. https://doi.org/10.2215/CJN.03400313.

    Article  PubMed  PubMed Central  Google Scholar 

  8. Copelovitch L, Nash MA, Kaplan BS. Hypothesis: Dent disease is an underrecognized cause of focal glomerulosclerosis. Clin J Am Soc Nephrol. 2007;2(5):914–8. https://doi.org/10.2215/CJN.00900207.

    Article  CAS  PubMed  Google Scholar 

  9. Beara-Lasic L, Cogal A, Mara K, Enders F, Mehta RA, Haskic Z, et al. Prevalence of low molecular weight proteinuria and Dent disease 1 CLCN5 mutations in proteinuric cohorts. Pediatr Nephrol. 2019. https://doi.org/10.1007/s00467-019-04210-0.

    Article  PubMed  PubMed Central  Google Scholar 

  10. Ceol M, Tiralongo E, Baelde HJ, Vianello D, Beetto G, Marangellis A, et al. Involvement of the tubular ClC-Type exchanger ClC-5 in glomeruli of human proteinuric nephropathies. PLoS ONE. 2012;7(9):3–9. https://doi.org/10.1371/journal.pone.0045605.

    Article  CAS  Google Scholar 

  11. Hryciw DH, Ekberg J, Pollock CA, Poronnik P. ClC-5: a chloride channel with multiple roles in renal tubular albumin uptake. Int J Biochem Cell Biol. 2006;38(7):1036–42. https://doi.org/10.1016/j.biocel.2005.09.009.

    Article  CAS  PubMed  Google Scholar 

  12. Norden AGW, Scheinman SJ, Deschodt-Lanckman MM, Lapsley M, Nortier JL, Thakker RV, et al. Tubular proteinuria defined by a study of Dent’s (CLCN5 mutation) and other tubular diseases. Kidney Int. 2000;57(1):240–9. https://doi.org/10.1046/j.1523-1755.2000.00847.x.

    Article  CAS  PubMed  Google Scholar 

  13. He G, Zhang H, Cao S, Xiao H, Yao Y. Dent’s disease complicated by nephrotic syndrome: a case report. Intractable Rare Dis Res. 2016;5(4):297–300. https://doi.org/10.5582/irdr.2016.01058.

    Article  PubMed  PubMed Central  Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Corresponding author

Correspondence to Katsuhiko Asanuma.

Ethics declarations

Conflicts of interest

No author has a direct conflict of interest that is relevant to this study. Outside the contents of the study, Katsuhiko Asanuma received research funding from Mitsubishi Tanabe Pharmaceutical Corporation.

Informed consent

Written informed consent was obtained from the patients, including consent to participate in a clinical study approved by Ethics Committee of Chiba University (approval number: Life-856) and to publish the findings.

Additional information

Publisher's Note

Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.

About this article

Check for updates. Verify currency and authenticity via CrossMark

Cite this article

Makino, S., Empitu, M.A., Naito, T. et al. A rare case of nephrotic syndrome associated with Dent’s disease: a case report. CEN Case Rep 9, 380–384 (2020). https://doi.org/10.1007/s13730-020-00491-9

Download citation

  • Received:

  • Accepted:

  • Published:

  • Issue Date:

  • DOI: https://doi.org/10.1007/s13730-020-00491-9

Keywords

Navigation