Interstitial cystitis: a rare manifestation of primary Sjögren’s syndrome, successfully treated with low dose cyclosporine
Makaleler > Vaka Takdimi · 2012
Yazarlar: Hakan Emmungil, Melike Kalfa, Figen YARGUCU ZİHNİ, Gonca KARABULUT, Gökhan KESER, Sait ŞEN, Kenan AKSU
RHEUMATOLOGY INTERNATIONAL, SCI Expanded İndekslerine Giren Dergi, Uluslararası, 2012, cilt 32, ss 1215-1218
Özet
<p>Chronic interstitial cystitis (IC), mostly affecting middle-aged women, is a very rare manifestation of primary Sjögren’s syndrome (pSS). Hereby, we report a 42-year-old woman with pSS, presenting with dysuria, urinary frequency, and suprapubic pain. She was diagnosed to have chronic IC, based upon the cystoscopic biopsy finding of chronic inflammation in the bladder wall. Systemic corticosteroid and azathioprine treatments together with local intravesical therapies were not effective. Therefore, cyclosporine (CSA) therapy was initiated. Initial low dose of CSA (1.5 mg/kg/d) improved the symptoms of the patient, with no requirement for dose increment. After 4 months of therapy, control cystoscopic biopsy showed that bladder inflammation regressed and IC improved. This case suggests that even low doses of CSA may be beneficial for treating chronic IC associated with pSS syndrome.</p>