Skip to main content

Advertisement

Log in

Diagnosis of monoclonal immunotactoid glomerulopathy with positive λ chain by immunoelectron microscopy

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

Abstract

We report the case of a 73-year-old-man who developed immunotactoid glomerulopathy (ITG). ITG is a rare disease characterized by proliferative glomerulonephritis and capillary wall deposits with a 10–60 nm diameter microtubular substructure. In monoclonal ITG, immunofluorescence analysis typically exhibits IgG with light chain restriction. Recent reviews recommend distinguishing monoclonal ITG from polyclonal ITG because monoclonal ITG is associated with a higher incidence of hematological disorders and better responsiveness to clone-directed therapy and renal prognosis. In our case, IgG, IgA, and IgM were negative by routine immunofluorescence; however, immunoelectron microscopy revealed positive λ chain. At 6 months after renal biopsy, the IgG λ chain was detected in the serum and urine, reflecting possible monoclonality. Therefore, it is useful to perform immunoelectron microscopy and follow-up with serum and urine protein electrophoresis and immunofixation to diagnose monoclonal ITG, even when routine immunofluorescence shows negative or nonspecific findings.

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.

Institutional subscriptions

Fig. 1
Fig. 2
Fig. 3
Fig. 4
Fig. 5

Similar content being viewed by others

References

  1. Korbet SMSM, Lewis EJ. Immunotactoid glomerulopathy. Am J Kidney Dis. 1991;17(3):247–57.

    Article  CAS  Google Scholar 

  2. Rosenstock JLMG, Valeri AM, Sacchi G, Appel GB, D’Agati VD. Fibrillary and immunotactoid glomerulonephritis: distinct entities with different clinical and pathologic features. Kidney Int. 2003;63(4):1450–61.

    Article  Google Scholar 

  3. Nasr SH, Kudose SS, Said SM, Santoriello D, Fidler ME, Williamson SR, et al. Immunotactoid glomerulopathy is a rare entity with monoclonal and polyclonal variants. Kidney Int. 2021;99(2):410–20. https://doi.org/10.1016/j.kint.2020.07.037.

    Article  CAS  Google Scholar 

  4. Nasr SHFM, Cornell LD, Leung N, Cosio FG, Sheikh SS, Amir AA, Vrana JA, Theis JD, Dogan A, Sethi S. Immunotactoid glomerulopathy: clinicopathologic and proteomic study. Nephrol Dial Transplant. 2012;27(11):4137–46.

    Article  CAS  Google Scholar 

  5. Schwartz MMKS, Lewis EJ. Immunotactoid glomerulopathy. J Am Soc Nephrol. 2002;13(5):1390–7.

    Article  Google Scholar 

  6. Yang GC, Nieto R, Stachura I, Gallo GR. Ultrastructural immunohistochemical localization of polyclonal IgG, C3, and amyloid P component on the Congo red-negative amyloid-like fibrils of fibrillary glomerulopathy. Am J Pathol. 1992;141(2):409–19.

    CAS  Google Scholar 

  7. Kinomura MMY, Makino H. A case of immunotactoid glomerulopathy exhibiting nephrotic syndrome successfully treated with corticosteroids and antihypertensive therapy. Clin Exp Nephrol. 2009;13(4):7.

    Article  Google Scholar 

  8. Inotani S, Horino T, Ishihara M, Ichii O, Matsumori A. Immunotactoid glomerulopathy associated with monoclonal gammopathy. Lancet. 2021;397(10289):2081. https://doi.org/10.1016/s0140-6736(21)00477-3.

    Article  Google Scholar 

  9. Hirashio S. A case of immunotactoid glomerulopathy with false-negative IgG staining. BMC Nephrol. 2018;19:143.

    Article  Google Scholar 

  10. Nasr SH, Larsen CP, Sirac C, Theis JD, Domenger C, Chauvet S, et al. Light chain only variant of proliferative glomerulonephritis with monoclonal immunoglobulin deposits is associated with a high detection rate of the pathogenic plasma cell clone. Kidney Int. 2020;97(3):589–601. https://doi.org/10.1016/j.kint.2019.10.025.

    Article  CAS  Google Scholar 

  11. Komatsuda A, Nara M, Ohtani H, Nimura T, Sawada K, Wakui H. Proliferative glomerulonephritis with monoclonal immunoglobulin light chain deposits: a rare entity mimicking immune-complex glomerulonephritis. Intern Med. 2012;51(23):3273–6. https://doi.org/10.2169/internalmedicine.51.8513.

    Article  Google Scholar 

  12. Hogan JJ, Vogl DT. Untangling immunotactoid glomerulopathy in the MGRS era. Kidney Int. 2021;99(2):303–5. https://doi.org/10.1016/j.kint.2020.09.013.

    Article  CAS  Google Scholar 

  13. Leung N, Bridoux F, Batuman V, Chaidos A, Cockwell P, D’Agati VD, et al. The evaluation of monoclonal gammopathy of renal significance: a consensus report of the International Kidney and Monoclonal Gammopathy Research Group. Nat Rev Nephrol. 2019;15(1):45–59. https://doi.org/10.1038/s41581-018-0077-4.

    Article  Google Scholar 

  14. Sethi S, Theis JD, Vrana JA, Fervenza FC, Sethi A, Qian Q, et al. Laser microdissection and proteomic analysis of amyloidosis, cryoglobulinemic GN, fibrillary GN, and immunotactoid glomerulopathy. Clin J Am Soc Nephrol. 2013;8(6):915–21. https://doi.org/10.2215/cjn.07030712.

    Article  CAS  Google Scholar 

  15. Morimoto N, Nagahama K, Oyama S, Tsuura Y, Fukutomi T, Terai A, et al. Immunotactoid glomerulonephritis in a patient with cold agglutinins: causal association or mere coincidence? CEN Case Rep. 2021;10(4):515–22. https://doi.org/10.1007/s13730-021-00600-2.

    Article  Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Corresponding author

Correspondence to Takeshi Kanda.

Ethics declarations

Conflict of interest

The authors declare that they have no conflicts of interest.

Ethical approval

This article does not contain any studies with human participants performed by any of the authors.

Informed consent

The authors obtained informed consent from the patient for publication of this case report and accompanying images.

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

Sugita, E., Sonoda, H., Ryuzaki, M. et al. Diagnosis of monoclonal immunotactoid glomerulopathy with positive λ chain by immunoelectron microscopy. CEN Case Rep 12, 7–13 (2023). https://doi.org/10.1007/s13730-022-00714-1

Download citation

  • Received:

  • Accepted:

  • Published:

  • Issue Date:

  • DOI: https://doi.org/10.1007/s13730-022-00714-1

Keywords

Navigation