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Review
. 2008 Apr;29(4):311-4.
doi: 10.1016/j.revmed.2007.09.028. Epub 2007 Oct 22.

[Osteomalacia revealing Sjögren's syndrome: a case report]

[Article in French]
Affiliations
Review

[Osteomalacia revealing Sjögren's syndrome: a case report]

[Article in French]
M Jallouli et al. Rev Med Interne. 2008 Apr.

Abstract

Introduction: The most common renal disease in Sjögren's syndrome is tubulo-interstitial nephritis, responsible for tubular acidosis in around 20 % of patients. Osteomalacia exceptionally occurs as the first manifestation of a renal tubule disorder due to a Sjögren's syndrome.

Exegesis: We report a case of a 20-year-old woman with tubular acidosis induced osteomalacia secondary to primary Sjögren's syndrome. Improvement was obtained with bicarbonates, vitamin D, calcium and high-dose steroid therapy.

Conclusion: During Sjögren's syndrome, osteomalacia can complicate the distal renal tubular acidosis. In spite of the rare cases of osteomalacia revealing Sjögren's syndrome, this auto-immune disease must appear in the list of the aetiologies of osteomalacia.

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