Osteomalacia revealing Sjogren's syndrome: A case report

被引：7

作者：

Jallouli, M. ^{[1
]}

Frigui, M. ^{[1
]}

Marzouk, S. ^{[1
]}

Kaddour, N. ^{[1
]}

Kechaou, M. ^{[1
]}

Frikha, F. ^{[1
]}

Bahloul, Z. ^{[1
]}

机构：

[1] CHU Hedi Chaker, Serv Med Interne, Sfax 3029, Tunisia

来源：

REVUE DE MEDECINE INTERNE | 2008年 / 29卷 / 04期

关键词：

Sjogren's syndrome; Osteomalacia; renal tubular acidosis;

D O I：

10.1016/j.revmed.2007.09.028

中图分类号：

R5 [内科学];

学科分类号：

1002 ; 100201 ;

摘要：

Introduction. - The most common renal disease in Sjogren'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 Sjogren's syndrome. Exegesis. - We report a case of a 20-year-old woman with tubular acidosis induced osteomalacia secondary to primary Sjogren's syndrome. Improvement was obtained with bicarbonates, vitamin D, calcium and high-dose steroid therapy. Conclusion: During Sjogren's syndrome, osteomalacia can complicate the distal renal tubular acidosis. In spite of the rare cases of osteomalacia revealing Sjogren's syndrome, this auto-immune disease must appear in the list of the aetiologies of osteomalacia. (C) 2007 Elsevier Masson SAS. Tous droits reserves.

引用

页码：311 / 314

页数：4

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