| Literature DB >> 35699924 |
Erina Sugita1, Homare Sonoda1, Masaki Ryuzaki1, Akinori Hashiguchi2, Hirobumi Tokuyama3, Shu Wakino4, Takeshi Kanda5, Hiroshi Itoh1.
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.Entities:
Keywords: Clinical nephrology; Immunotactoid glomerulopathy; Nephrotic syndrome
Year: 2022 PMID: 35699924 DOI: 10.1007/s13730-022-00714-1
Source DB: PubMed Journal: CEN Case Rep ISSN: 2192-4449