Saito Ayano, Kameoka Yoshihiro, Ubukawa Kumi, Ohtani Hiroshi, Abe Fumito, Saito Masaya, Hashimoto Mako, Kanazawa Tatsuro, Komatsuda Atsushi, Takahashi Naoto
Department of Hematology, Nephrology, and Rheumatology, Akita University Graduate School of Medicine, Japan.
Department of Internal Medicine, Yuri-Kumiai General Hospital, Japan.
Intern Med. 2025 May 1;64(9):1388-1392. doi: 10.2169/internalmedicine.3902-24. Epub 2024 Oct 4.
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.
一名71岁女性在慢性淋巴细胞白血病10年随访期间出现肾病综合征。肾活检样本分析显示为IgG1-λ阳性单克隆免疫触须样肾小球病(mITG)。该患者接受了布鲁顿酪氨酸激酶抑制剂伊布替尼治疗,24个月后实现了完全肾脏缓解。免疫触须样肾小球病是一种以肾小球沉积为特征的罕见疾病。特别是mITG,其呈现出具有轻链限制的免疫沉积物,常与血液系统疾病相关。大多数mITG患者接受免疫抑制治疗和/或化疗;然而,据我们所知,尚无伊布替尼治疗的报道。