Hewitt Daniel, Tait Clare
Department of Dermatology, Royal Perth Hospital, Western Australia, Australia.
Australas J Dermatol. 2007 May;48(2):95-8. doi: 10.1111/j.1440-0960.2007.00344.x.
A 57-year-old man, with a 2-year history of Crohn's disease, presented with a rapidly progressive abdominal ulcer. It was clinically and histologically consistent with pyoderma gangrenosum but it did not respond to either high-dose oral prednisolone or intravenous hydrocortisone. Infliximab resulted in an early, dramatic and sustained improvement. His bowel symptoms, which flared a few weeks prior to the onset of pyoderma gangrenosum, only partially improved. Despite six infliximab infusions, the inflammatory bowel disease is poorly controlled, whereas the pyoderma gangrenosum remains healed.
一名57岁男性,有2年克罗恩病病史,出现迅速进展的腹部溃疡。临床和组织学表现均符合坏疽性脓皮病,但对大剂量口服泼尼松龙或静脉注射氢化可的松均无反应。英夫利昔单抗治疗后早期即有显著且持续的改善。他在坏疽性脓皮病发作前几周出现的肠道症状仅部分改善。尽管进行了6次英夫利昔单抗输注,炎症性肠病仍控制不佳,而坏疽性脓皮病已愈合。