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.
Similar content being viewed by others
References
Korbet SMSM, Lewis EJ. Immunotactoid glomerulopathy. Am J Kidney Dis. 1991;17(3):247–57.
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.
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.
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.
Schwartz MMKS, Lewis EJ. Immunotactoid glomerulopathy. J Am Soc Nephrol. 2002;13(5):1390–7.
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.
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.
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.
Hirashio S. A case of immunotactoid glomerulopathy with false-negative IgG staining. BMC Nephrol. 2018;19:143.
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.
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.
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.
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.
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.
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.
Author information
Authors and Affiliations
Corresponding author
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
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
Received:
Accepted:
Published:
Issue Date:
DOI: https://doi.org/10.1007/s13730-022-00714-1