Interstitial cystitis in case of primary Sjogren's syndrome

M. Higuchi, T. Migita, S. Yoshizawa, T. Horiuchi, H. Nakashima, Y. Niho

研究成果: ジャーナルへの寄稿記事

6 引用 (Scopus)

抜粋

A 53-year-old woman who had xerostomia for ten years was admitted to our hospital because of refractory lower abdominal pain and pollakisuria of five years duration. Although she had undergone surgical treatments including cholecystectomy, ovarian cystectomy and groin hemiorrhaphy, she still suffered from abdominal symptoms. A diagnosis of interstitial cystitis was confirmed by hydraulic distention during a cystoscopic examination and by histopathological examination of the bladder. Her symptoms disappeared soon after the cystoscopic procedure, which also had a therapeutic effect of interstitial cystitis. Laboratory findings revealed hypergammaglobulinemia, a high titer of rheumatoid factor, positive anti-nuclear antibody, and positive anti-SS-A/Ro antibody. She was diagnosed as having primary Sjogren's syndrome based on the results of a gum test (8.5 ml/10 min), sialography (Stage II), and a positive minor salivary gland biopsy. Starting one month after the hydraulic distention, her abdominal symptoms gradully reappeared along with elevation of her serum IgG level. These features were markedly improved with 30 mg/day of oral prednisolone, which was then successfully tapered. These results suggested that interstitial cystitis in this case was caused by immunological abnormalities associated with Sjogren's syndrome.

元の言語英語
ページ(範囲)34-38
ページ数5
ジャーナルRyumachi
38
発行部数1
出版物ステータス出版済み - 5 9 1998

    フィンガープリント

All Science Journal Classification (ASJC) codes

  • Rheumatology

これを引用

Higuchi, M., Migita, T., Yoshizawa, S., Horiuchi, T., Nakashima, H., & Niho, Y. (1998). Interstitial cystitis in case of primary Sjogren's syndrome. Ryumachi, 38(1), 34-38.