J Korean Soc Pediatr Nephrol.  2002 Oct;6(2):155-168.

Clinical Manifestation and Treatment Outcome of Lupus Nephritis in Children

Affiliations
  • 1Department of Pediatrics, Yonsei University College of Medicine, Seoul, Korea. jsyonse@yumc.yonsei.ac.kr

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.

Keyword

Lupus nephritis; WHO class IV; Aggressive treatment

MeSH Terms

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*
Cyclophosphamide
DNA
Prednisolone
gamma-Globulins
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