Membranous Nephropathy in a 13-Year-Old Boy with Common Variable Immunodeficiency.
10.3346/jkms.2012.27.11.1436
- Author:
Hyung Eun YIM
1
;
Kee Hwan YOO
Author Information
1. Department of Pediatrics, Korea University Medical Center, Seoul, Korea. guroped@korea.ac.kr
- Publication Type:Case Reports
- Keywords:
Autoimmunity;
Common Variable Immunodeficiency;
Immunoglobulins;
Membranous Glomerulonephritis
- MeSH:
Adolescent;
Bronchiectasis/etiology;
Common Variable Immunodeficiency/complications/*diagnosis/drug therapy;
Cyclosporine/therapeutic use;
Drug Therapy, Combination;
Glomerulonephritis, Membranous/complications/*diagnosis/drug therapy;
Humans;
Immunoglobulins/therapeutic use;
Immunosuppressive Agents/therapeutic use;
Injections, Intravenous;
Kidney/pathology;
Male;
Pneumonia/etiology;
Proteinuria/etiology;
Steroids/therapeutic use
- From:Journal of Korean Medical Science
2012;27(11):1436-1438
- CountryRepublic of Korea
- Language:English
-
Abstract:
Various forms of hypogammaglobulinemia can occur in patients with autoimmune diseases and vice versa. We report a 13-yr-old boy with membranous nephropathy and common variable immunodeficiency. He presented with the nephrotic syndrome, pneumonia with bronchiectasis, and profound hypogammaglobulinemia. Renal biopsy showed diffusely thickened glomerular capillary walls with 'spikes' suggesting a membranous nephropathy. Secondary causes were ruled out by laboratory studies; however, heavy proteinuria persisted with steroid therapy. Cyclosporine and intravenous immunoglobulin were added, and the patient was discharged with decreased proteinuria. Hypogammaglobulinemia may have a deleterious impact on the immune dysregulation in some patients with membranous nephropathy.
