ArticleBMJ case reports2025
The challenges of managing distal renal tubular acidosis in pregnant patients with primary Sjögren's disease.
Article in BMJ case reports, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.
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Who cites it
2 citing papers in PubMed.
- Sjögren's Disease-Associated Renal Tubular Acidosis: An Integrated Immuno-Tubular Model of Tubular Dysfunction.International journal of medical sciences · 2026Review
- Distal Renal Tubular Acidosis in Pregnancy: A Case Report and Systematic Literature Review.European journal of case reports in internal medicine · 2026Article
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Authors and funding
4 authors.
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Abstract
We present a case of a pregnant woman in her 40 s diagnosed with primary Sjögren's disease (pSjD) complicated by distal type I renal tubular acidosis. At 12 weeks' gestation, she exhibited dry eyes, dry mouth and renal dysfunction for the first time. Electrolyte studies confirmed hyperchloraemic normal anion gap metabolic acidosis with elevated urine pH. Positive serologies included +ANA, +SSA and +RF. Schirmer's test was positive. Renal biopsy indicated chronic tubulointerstitial nephritis with 40% interstitial fibrosis. Hydroxychloroquine and prednisone (60 mg daily) improved renal function, but rapid tapering led to mild worsening in renal function, sicca symptoms and fetal growth restriction. Steroid dose escalation and azathioprine initiation led to clinical improvements. At 35 weeks' gestation, she delivered preterm due to pre-eclampsia and intrahepatic cholestasis. The neonate had cutaneous neonatal lupus but was otherwise healthy. This case highlights the clinical complexity of managing distal renal tubular acidosis in pregnant patients with pSjD and the need for evidence-based treatment guidelines.
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