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Filgrastim-Induced Crescentic Transformation of Recurrent IgG2λ GN
Ibrahim Batal1, Glen S Markowitz2, Waichi Wong3
1Renal Pathology, Department of Pathology and Cell Biology, ib2349@columbia.edu.
This case study highlights a rare proliferative glomerulonephritis with monoclonal IgG deposits. Filgrastim (G-CSF) exacerbated the patient's kidney disease and led to allograft failure, suggesting a link to plasma cell neoplasms.
Area of Science:
- Nephrology
- Hematology
- Immunology
Background:
- Proliferative glomerulonephritis with monoclonal IgG deposits is an emerging entity.
- Its association with hematologic malignancies requires further elucidation.
- Granulocyte colony-stimulating factor (G-CSF) is used for hematopoietic progenitor cell mobilization.
Observation:
- A young man presented with slow-progressing proliferative GN and monoclonal IgG2λ deposits.
- He developed recurrent GN post-kidney transplant and a plasma cell neoplasm 9 years later.
- G-CSF administration for stem cell mobilization coincided with severe crescentic transformation of the GN.
Findings:
- The patient experienced rapid allograft failure following G-CSF treatment.
- This suggests G-CSF may exacerbate pre-existing GN in patients with monoclonal IgG deposits.
- A potential link between G-CSF, GN, and plasma cell neoplasms is indicated.
Implications:
- This case underscores the importance of considering hematologic malignancies in proliferative GN with monoclonal IgG deposits.
- It raises concerns about the use of G-CSF in patients with underlying renal disease and potential plasma cell neoplasms.
- Further research is needed to understand the pathophysiologic role of G-CSF in GN exacerbation.
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