Cyclophosphamide therapy in Sweet's syndrome complicating refractory Crohn's disease - Efficacy and mechanism of action

被引:5
|
作者
Meinhardt, Christian [1 ]
Buening, Juergen [1 ]
Fellermann, Klaus [1 ]
Lehnert, Hendrik [1 ]
Schmidt, Klaus J. [1 ]
机构
[1] Univ Hosp Schleswig Holstein, Dept Internal Med 1, D-23538 Lubeck, Germany
关键词
Sweets syndrome; Crohn's disease; Apoptosis; TUNEL; INFLAMMATORY-BOWEL-DISEASE; NECROSIS-FACTOR; AZATHIOPRINE HYPERSENSITIVITY; ULCERATIVE-COLITIS; ERYTHEMA-NODOSUM; PULSE THERAPY; MANIFESTATION; LYMPHOCYTES; APOPTOSIS;
D O I
10.1016/j.crohns.2011.07.014
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Background: Sweet's syndrome is a rare extraintestinal manifestation of Crohn's disease that is usually treated by corticosteroids. Cyclophosphamide therapy has been shown to be effective in steroid-refractory Crohn's disease with extraintestinal manifestations. The mechanism of action remains obscure. Here, we report about a case of steroid-refractory Sweet's syndrome accompanying Crohn's colitis treated by cyclophosphamide. Methods: At baseline and two weeks after initiating cyclophosphamide pulse therapy, clinical symptoms were evaluated and apoptosis in mononuclear cells of the colon mucosa was quantified via immunofluorescence TUNEL-labeling. Ongoing clinical follow-up lasts for more than three years. Results: Cyclophosphamide pulse therapy resulted in complete resolution of luminal activity and extraintestinal manifestations. TUNEL-marked CD4(+), CD8(+) and CD68(+) cells in intestinal biopsies showed a 338% increase as compared to baseline. Conclusions: Cyclophosphamide therapy was highly effective in steroid-refractory Crohn's colitis accompanied by Sweets syndrome for induction of remission. Furthermore, apoptosis of mononuclear cells in the colon mucosa, including CD68(+) macrophages as well as CD4(+) and CD8(+) cells, appears to be a component of the anti-inflammatory effect of cyclophosphamide in Crohn's disease. (C) 2011 European Crohn's and Colitis Organisation. Published by Elsevier B.V. All rights reserved.
引用
收藏
页码:633 / 637
页数:5
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