A Case of Type 1 Renal Tubular Acidosis and Osteomalacia in a Patient with Sjogren's Syndrome.
10.4078/jrd.2012.19.4.220
- Author:
Ho Jun LEE
1
;
Sung Ji LEE
;
Seong Chang PARK
;
Dong Jin PARK
;
Tae Jong KIM
;
Shin Seok LEE
;
Yong Wook PARK
Author Information
1. Department of Rheumatology, Chonnam National University Medical School and Hospital, Gwangju, Korea. parkyw@jnu.ac.kr
- Publication Type:Case Report
- Keywords:
Sjogren's syndrome;
Renal tubular acidosis;
Osteomalacia
- MeSH:
Acidosis, Renal Tubular;
Adult;
Autoimmune Diseases;
Female;
Humans;
Lower Extremity;
Muscle Weakness;
Osteomalacia;
Salivary Glands;
Sjogren's Syndrome
- From:Journal of Rheumatic Diseases
2012;19(4):220-224
- CountryRepublic of Korea
- Language:Korean
-
Abstract:
Sjogren's syndrome is a chronic autoimmune disease characterized by decreased function of the lacrimal and salivary glands. In addition, many other organs can be involved in patients with Sjogren's syndrome. Overt or latent renal tubular acidosis is an uncommon extraglandular manifestation in Sjogren's syndrome, and osteomalacia is a rare complication of renal tubular acidosis. It has been rarely reported that osteomalacia is associated with distal renal tubular acidosis in patients with Sjogren's syndrome. We report a case of a 34-year-old female patient who was initially presented with muscle weakness in both lower extremities. The patient was then diagnosed with Sjogren's syndrome complicated by osteomalacia and renal tubular acidosis
