1. A case of monoclonal gammopathy of renal significance presenting as atypical amyloidosis with IgA lambda paraproteinemia
- Author
-
James Nolan, John Brealey, Anjelo Jobert, and Chankyung Kim
- Subjects
0301 basic medicine ,Immunoglobulin A ,Paraproteinemia ,Pathology ,medicine.medical_specialty ,Histology ,Amyloid ,Atypical amyloidosis ,Plasma cell ,Immunofluorescence ,Renal amyloidosis ,Pathology and Forensic Medicine ,03 medical and health sciences ,0302 clinical medicine ,lcsh:Pathology ,medicine ,Kidney ,Case Study ,medicine.diagnostic_test ,biology ,business.industry ,Amyloidosis ,medicine.disease ,AHL amyloidosis ,030104 developmental biology ,medicine.anatomical_structure ,030220 oncology & carcinogenesis ,biology.protein ,Monoclonal gammopathy of renal significance ,business ,lcsh:RB1-214 - Abstract
Monoclonal gammopathy of renal significance is defined as any B cell or plasma cell clonal lymphoproliferation which neither causes tumor complications nor meets any current hematological criteria for specific therapy, with one or more kidney lesions related to the produced monoclonal immunoglobulin, such as amyloidosis. A 50-year-old male presented with heavy proteinuria and blood tests showing IgA and Lambda paraproteinemia. Light microscopy showed mesangial eosinophilic ground substance extending into the capillary loops, and positive staining within the glomeruli and vessel walls for amyloid P immunohistochemistry was also noted. Immunofluorescence showed positive staining for IgA and Lambda in the mesangia and capillary loops. Electron microscopy exhibited organized fibrils measuring 4–5 nm in diameter in the mesangia, glomerular basement membranes and vessel walls. We interpreted the overall findings as atypical renal amyloidosis with IgA and Lambda deposition on immunofluorescence. Further amyloid typing using laser microdissection-liquid chromatography and mass spectrometry will be useful.
- Published
- 2020