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CO2-Lasertonsillotomy Under Local Anesthesia in Adults
Published on: November 6, 2019
MPO-ANCA-positive IgA nephropathy successfully treated with tonsillectomy
Noriko Ogawa1, Shozo Yano2, Yuko Yamane2
1First Department of Internal Medicine, Shimane University Faculty of Medicine, 89-1 Enya-cho, Izumo, Shimane, 693-8501, Japan. noriko.o@med.shimane-u.ac.jp.
IgA nephropathy activity and myeloperoxidase (MPO)-antineutrophil cytoplasmic antibody (ANCA) production may be linked to tonsillitis. Tonsillectomy improved IgA nephropathy and resolved MPO-ANCA positivity in this case.
Area of Science:
- Nephrology
- Immunology
- Internal Medicine
Background:
- IgA nephropathy (IgAN) is a common cause of glomerulonephritis, often associated with hematuria and proteinuria.
- Myeloperoxidase (MPO)-antineutrophil cytoplasmic antibody (ANCA) positivity can indicate systemic vasculitis but its role in IgAN is less understood.
- Recurrent infections, such as tonsillitis, have been implicated in IgAN flares.
Observation:
- A 20-year-old Japanese woman with IgAN presented with gross hematuria and crescents on biopsy, initially negative for MPO-ANCA.
- Despite treatment, proteinuria increased, coinciding with recurrent tonsillitis and the emergence of MPO-ANCA positivity.
- Following tonsillectomy and low-dose prednisolone, proteinuria significantly improved, creatinine clearance normalized, and MPO-ANCA became undetectable.
Findings:
- This case demonstrates a potential association between tonsillitis, IgA nephropathy activity, and MPO-ANCA production.
- Resolution of tonsillitis correlated with clinical improvement in IgAN and serological normalization of MPO-ANCA.
- The findings suggest that infections may trigger or exacerbate IgAN and influence MPO-ANCA status.
Implications:
- Tonsillectomy may be a therapeutic option for IgA nephropathy patients with concurrent tonsillitis and MPO-ANCA positivity.
- Further research is warranted to elucidate the mechanisms linking infection, IgAN, and MPO-ANCA.
- This case highlights the importance of considering infectious triggers in the management of IgA nephropathy.
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