Successful Treatment of Monoclonal Immunotactoid Glomerulopathy Associated with Chronic Lymphocytic Leukemia Using Ibrutinib
A 71-year-old woman developed nephrotic syndrome during 10-year follow-up for chronic lymphocytic leukemia. A renal biopsy sample analysis revealed IgG1-lambda-positive monoclonal immunotactoid glomerulopathy (mITG). The patient was treated with ibrutinib, a Bruton tyrosine kinase inhibitor, and complete renal remission was achieved after 24 months. ITG is a rare disease that is characterized by glomerular deposition. In particular, mITG, which presents immune deposits that exhibit light-chain restriction, is often associated with hematologic disorders. Most patients with mITG receive immunosuppressive therapy and/or chemotherapy; however, to our knowledge, there have been no reports of treatment with ibrutinib.
Authors
- Kumi Ubukawa
- Masaya Saito (ORCID: https://orcid.org/0000-0002-4840-6515)
- Fumito Abe (ORCID: https://orcid.org/0000-0002-8427-5604)
- Naoto Takahashi (ORCID: https://orcid.org/0000-0002-6758-3787)
- Yoshihiro Kameoka (ORCID: https://orcid.org/0000-0002-6786-3439)
- Atsushi Komatsuda (ORCID: https://orcid.org/0000-0003-1477-8131)
- Hiroshi Ohtani (ORCID: https://orcid.org/0000-0002-8951-159X)
- Ayano Saito
- Tatsuro Kanazawa
- Mako Hashimoto
Institutions
- Akita University (JP)
- Kumiai Chemical Industry (Japan) (JP)
Publication Details
- Journal
- Internal Medicine
- Published
- 2024-10-03
- DOI
- https://doi.org/10.2169/internalmedicine.3902-24
- Primary Topic
- Chronic Lymphocytic Leukemia Research
- Type
- article
- Field-Weighted Citation Impact
- 0.00