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Updated: Jan 7, 2026

Tumor Engraftment in a Xenograft Mouse Model of Human Mantle Cell Lymphoma
Published on: March 30, 2018
慢性リンパ性白血病を伴う単クローン性免疫タクチド糸球体症:症例報告
Gholamreza Badiee1, Atefeh Kalantary1, Sina Shafiei1
1Internal Medicine, David Geffen School of Medicine at UCLA (University of California, Los Angeles), Los Angeles, USA.
Abstract:
Immunotactoid glomerulopathy (ITG) is exceedingly rare in clinical practice. A majority of cases are associated with an underlying hematological disorder and specifically chronic lymphocytic leukemia (CLL). The treatment consists of managing the underlying disease and supportive therapy. We present the case of an 80-year-old patient with a history of CLL who presented with proteinuria and acute kidney injury and eventually developed hematuria. His renal biopsy revealed monoclonal ITG. He began a course of chemotherapy for CLL and achieved remission with improved renal function.
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