Clinical Manifestation and Treatment Outcome of Lupus Nephritis in Children.
- Author:
Jee Min PARK
1
;
Jae IL SHIN
;
Jae Seung LEE
;
Pyung Kil KIM
Author Information
1. Department of Pediatrics, Yonsei University College of Medicine, Seoul, Korea. jsyonse@yumc.yonsei.ac.kr
- Publication Type:Original Article
- Keywords:
Lupus nephritis;
WHO class IV;
Aggressive treatment
- MeSH:
Acute Kidney Injury;
Adult;
Autoimmune Diseases;
Biopsy;
Child*;
Classification;
Cyclophosphamide;
Diagnosis;
DNA;
Exanthema;
Female;
Follow-Up Studies;
gamma-Globulins;
Gonads;
Hematuria;
Humans;
Lupus Nephritis*;
Male;
Mortality;
Nephrotic Syndrome;
Plasma Exchange;
Prednisolone;
Prognosis;
Proteinuria;
Retrospective Studies;
Risk Factors;
Treatment Outcome*
- From:Journal of the Korean Society of Pediatric Nephrology
2002;6(2):155-168
- CountryRepublic of Korea
- Language:Korean
-
Abstract:
PURPOSE: Systemic lupus erythematosus(SLE) is an autoimmune disease with multi-system involvement and renal damage is a major cause of morbidity and mortality in children. Renal involvement is more common and severe in children than in adults. Therefore, renal biopsy plays a crucial role in planning effective therapy. In this study, we investigated the clinical and pathological findings of lupus nephritis in children to aid clinical care of the disease. METHODS: The clinical and pathological data of 40 patients who were diagnosed as SLE with renal involvement in Shinchon Severance Hospital from Jan. 1990 to Sep. 2002 were analyzed retrospectively. RESULTS: The ratio of male to female patients was 1:3 and the median age at diagnosis was 12.1 (2-18) years old. FANA(95.0%), anti-ds DNA antibody (87.5%), malar rash (80.0%) were the most common findings among the classification criteria by ARA. Microscopic hematuria with proteinuria (75.0%), nephrotic syndrome (55.0%), and microscopic hematuria alone (15.0%) were the most common renal presentations in the respective order at diagnosis. There were 27 cases with WHO class IV lupus nephritis confirmed by renal biopsy and 3 cases with pathological changes of WHO class type. Different treatment modalities were carried out : prednisolone only in 5 cases, prednisol-one+azat-hioprine in 9 cases, prednisolone+azathioprine+intravenous cyclophosphamide in 14 cases, prednisolone+cyclosporine A+intravenous cyclophosphamide in 12 cases, plasma exchange in 9 cases and intravenous gamma-globulin in 2 cases. The average follow-up period was 51.8 40.5 months. During 51.8+/-40.5 months. During follow-up, 4 patients expired. The risk factors associated with mortality were male, WHO class IV and acute renal failure at diagnosis. CONCLUSION: Renal involvement was noted in 63.5% of childhood SLE, and 67.5% of renal lesion was WHO class IV lupus nephritis which is known to be associated with a poor prognosis. Therefore aggressive treatment employing immunosuppressant during the early stages of disease could be helpful in improving long-term prognosis. But careful attention should be given to optimize the treatment due to unique problems associated with growth, psychosocial development and gonadal toxicity, especially in children.
