Abstract
Objectives:
Kidney lesions at lymphoproliferative diseases mainly described with disease progression or relapse. Renal involvement in the manifestation of lymphoproliferative diseases were observed rarely. Pathogenesis of renal damage is obscure.
Aim: To determine especially renal damage in the manifestation of lymphoproliferative diseases.
Subjects and methods. The study included 19 patients (13 males, and 6 females, age 63.3±8.8 years) with lymphoproliferative diseases accompanied by renal failure: chronic lymphocytic leukemia (n=12), marginal zone lymphoma (n=4), follicular lymphoma (n=1), Waldenstrom's macroglobulinemia (n=1), diffuse large B-cell lymphoma (n=1). Nephrotic syndrome was observed in 3 patients and renal failure in 18 ones. The average creatinine level was 330.9±152.3 μmol/l, glomerular filtration rate was 25.7±12.9 ml/min. The presence of monoclonal IgMk secretion (n=6), Bence Jones protein kappa (n=9), increased level of free light chains (n=4), cryoglobulin (n=4). The renal biopsy was studied by histological, immunohistochemical, immunofluorescence, and electron microscopy.
Results:Glomerulonephritises were revealed in 10 cases (52.6%): membranoproliferative glomerulonephritis (n=2), membranous (n=2), mesangiocapillary (n=3), fibrillary (n=1), immunotactoid glomerulonephritis (n=1), minimal-change disease (n=1). Neoplastic lymphoid infiltration of renal parenchyma was detected in 10 (52.6%) cases. The massive diffuse small cell lymphoid proliferation was determined in 1 case, focal infiltration in 9 ones. Neoplastic lymphoid infiltration was associated with glomerulonephritis in 3 cases and with carcinoma of the kidney in 4 cases. Large focal lymphoid proliferation was found in 1 case in a patient with diffuse large B-cell lymphoma. AL - amyloidosis was identified in 2 cases and the thrombotic microangiopathies in 2 ones.
Conclusion. Glomerular disease, lymphoid tumor infiltration, sometimes AL - amyloidosis, thrombotic microangiopathy were detected in the manifestation of lymphatic tumor. In all cases examined, there was a secretion of monoclonal immunoglobulin, protein Bence Jones, free light chains and cryoglobulin, pathogenetic value in the development of glomerulopathy should be clarified.
No relevant conflicts of interest to declare.
Author notes
Asterisk with author names denotes non-ASH members.