A Case of Distal Renal Tubular Acidosis with Systemic Lupus Erythematosus (SLE).
- Author:
Jeong Hwa CHOI
1
;
Sung Hun KIM
;
Young Tak LIM
;
Su Yung KIM
Author Information
1. Department of Pediatrics, College of Medicine, Pusan National University, Pusan, Korea.
- Publication Type:Case Report
- Keywords:
Distal renal tubular acidosis;
Systemic lupus erythematosus
- MeSH:
Abdominal Pain;
Acidosis;
Acidosis, Renal Tubular*;
Adolescent;
Alkalies;
Anemia, Hemolytic;
Atrophy;
Biopsy;
Chest Pain;
Child, Preschool;
Diagnosis*;
Exanthema;
Female;
Fever;
Fibrosis;
Hospitalization;
Humans;
Hypergammaglobulinemia;
Hypokalemia;
Intestinal Volvulus*;
Leukopenia;
Liver Diseases;
Lupus Erythematosus, Systemic*;
Lymphopenia;
Melena;
Mesentery;
Molecular Weight;
Multiple Myeloma;
Nephrotic Syndrome;
Neutrophils;
Potassium;
Prednisolone;
Proteinuria;
Thyroid Diseases;
Tomography, X-Ray Computed*
- From:Journal of the Korean Pediatric Society
1997;40(1):140-145
- CountryRepublic of Korea
- Language:Korean
-
Abstract:
Distal renal tubular acidosis (RTA) is well-recognized complication of immunologically mediated condition such as Sj ogren's syndrome, SLE, idiopathic hypergammaglobulinemia, autoimmune liver disease, autoimmune thyroid disease, multiple myeloma, and renal tranplant rejection. Tubulointerstitial involvement frequently occurrs in SLE. A sepctrum of abnormalities including impaired uriary concentration or acidification, increased fractional excretion of low molecular weight protein, hyporeinaemic hypoaldosteroniam and impaired tubular potassium excretion can occur in SLE. But complete distal RTA associated wih SLE is rare. We report a 13 year-old female with SLE and distal RTA which was diagnosed by NaHCO3 loading test. She had nephrotic syndrome, hypokalemia, hyperchloremic metabolic acidosis with alkali urine. She had fatiquebility, general weakness, intermittent fever and chest pain for at least 12months. And then, the butterfly-shaped malar rash was developed, so pediatrician suspected SLE and she was refer to us. At hospitalization. She had malar rash, percardial effusion, persistent proteinuria greater than 3+, hemolytic anemia, lymphopenia, leukopenia, positive LE cell, Anti-DNA Ab and posotive ANA. So her clinical data are satisfied ARA criteria for SLE. Her renal biopsy showed diffuse proliferative SLE nephpritis and marked focal tubular atrophy with localized heavy mononuclear cell infiltration and fibrosis. We performed NaHCO3 loading test to confirm distal RTA. During the test, we detected the inability to achieve a high urinary PCO2. This result is the most sensitive index of impaired distal acidification, so we can diagnose distal RTA. She had a good response to the therapy with prednisolone NaHCO3 and oral KCL supplement.
