Literature DB >> 16305106

[Distal renal tubular acidosis as a cause of osteomalacia in a patient with primary Sjögren's syndrome].

Aleksandra Jovelić1, Dusan Stefanović.   

Abstract

BACKGROUND: One half of the patients with primary Sjögren's syndrome has extraglandular manifestations, including renal involvement. The most frequent renal lesion is tubulo-interstitial nephritis, which manifests clinically as distal tubular acidosis and may result in the development of osteomalacia. CASE REPORT: In a 29-year-old female patient, with bilateral nephrolithiasis, the diagnosis of primary Sjögren's syndrome, tubulo-interstitial nephritis, distal renal tubular acidosis, and hypokalemia were established. She was treated for hypokalemia. Two years later she developed bone pains and muscle weakness, she wasn't able to walk, her proximal muscles and pelvic bones were painful, with radiological signs of pelvic bones osteopenia and pubic bones fractures. The diagnosis of osteomalacia was established and the treatment started with Schol's solution, vitamin D and calcium. In the following two months, acidosis was corrected, and the patient started walking.
CONCLUSION: In our patient with primary Sjögren's syndrome and interstitial nephritis, osteomalacia was a result of the long time decompensate acidosis, so the correction of acidosis, and the supplementation of vitamin D and calcium were the integral part of the therapy.

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Year:  2005        PMID: 16305106     DOI: 10.2298/vsp0510769j

Source DB:  PubMed          Journal:  Vojnosanit Pregl        ISSN: 0042-8450            Impact factor:   0.168


  1 in total

1.  Acquired hypophosphatemia osteomalacia associated with Fanconi's syndrome in Sjögren's syndrome.

Authors:  Yi-Sun Yang; Chiung-Huei Peng; Sung-Kien Sia; Chien-Ning Huang
Journal:  Rheumatol Int       Date:  2006-11-09       Impact factor: 2.631

  1 in total

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