EFFICACY AND SAFETY OF ORAL CYCLOSPORIN IN TREATMENT OF PYODERMA GANGRENOSUM
Abstract
INTRODUCTION: Pyoderma gangrenosum (PG) is an idiopathic, non-infectious ulcerating disorder predominantly involving skin, with primarily neutrophilic inflammatory infiltrate. The mainstay of therapy for PG has been high-dose corticosteroids but systemic agents such as cyclophosphamide, cyclosporine or azathioprine can be used.
AIMS: To evaluate efficacy and safety of oral cyclosporine in patients with pyoderma gangrenosum.
MATERIALS AND METHOD: A retrospective study of patients presenting with pyoderma gangrenosum from February 2014 to February 2018 was carried out. All patients were given oral cyclosporine 3 mg/kg/day for minimum 6 weeks to maximum 12 weeks as per requirement. At the end of therapy patients were classified according to response and reduction ulcer area score.
RESULTS: Ulcer area in each patient reduced above 60% with minimal side effects after giving cyclosporine for 12 weeks. Out of 27 patients, 12 had excellent response (>90%). While 10 patients had good response (70-90 %) and 5 had good response (50-70%).
CONCLUSION: This study shows that systemic low dose cyclosporine is an effective and safe treatment option available for pyoderma gangrenosum.
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