| Literature DB >> 33392216 |
Giacomo Quattrocchio1, Antonella Barreca2, Antonella Vaccarino3, Giulio Del Vecchio1, Emanuele De Simone1, Roberta Fenoglio1, Michela Ferro1, Maria Pagliaro3, Massimo Pini3, Massimo Manes4, Dario Roccatello1,5.
Abstract
Monoclonal Gammopathy of Renal Significance (MGRS) is a group of heterogeneous disorders characterized by renal dysfunction secondary to the production of a monoclonal immunoglobulin by a nonmalignant B cell or plasma cell clone. We report the clinical and histological outcomes of two patients with biopsy-proven MGRS: one patient showed membranoproliferative glomerulonephritis with monoclonal k-light chain and C3 deposits, the second patient showed immunotactoid glomerulopathy. Both patients were treated with a 9-month chemotherapy protocol including bortezomib, cyclophosphamide, and dexamethasone. Renal biospy was repeated after 1 year. The estimated glomerular filtration rate (eGFR) increased from 22.5 (baseline) to 40 ml/min per 1.73 m2 after 12 months, then to 51.5 ml/min per 1.73 m2 after 24 months; proteinuria decreased from 4.85 (baseline) to 0.17 g/day after 12 months, then to 0.14 g/day after 24 months. Repeat renal biopsies showed a dramatic improvement of the glomerular proliferative lesions and near complete disappearance of the immune deposits. A bortezomib-based treatment proved very effective and was well-tolerated in the two patients presenting with clinically and histologically aggressive MGRS.Entities:
Keywords: C3 glomerulonephritis (C3GN); Immunotactoid glomerulonephritis; bortezomib; glomerulonephritis; monoclonal gammopathy of renal significance (MGRS)
Year: 2020 PMID: 33392216 PMCID: PMC7772466 DOI: 10.3389/fmed.2020.587345
Source DB: PubMed Journal: Front Med (Lausanne) ISSN: 2296-858X