Wcisło-Dziadecka Dominika, Bergler-Czop Beata, Brzezińska-Wcisło Ligia, Arasiewicz Hubert
Medical Univesity of Silesia, School of Medicine in Katowice, Department of Cosmetology, Institute of Structural Research of Skin, Katowice, Poland. Head of Department: Krzysztof Jasik PhD.
Medical Univesity of Silesia, School of Medicine in Katowice, Chair and Department of Dermatology, Katowice, Poland. Head of Department: Prof. Ligia Brzezińska-Wcisło MD, PhD.
Postepy Dermatol Alergol. 2015 Feb;32(1):46-50. doi: 10.5114/pdia.2014.40947. Epub 2015 Feb 4.
Pyoderma gangrenosum (PG) is a relatively rare neutrophilic dermatosis, characterized by progressive skin necrosis. It typically has a chronic course, of unknown etiology. Pyoderma gangrenosum diagnosis can be difficult because both histopathological examination and results of additional laboratory tests are not specific and the clinical state is conclusive, as for other physicians it poses a number of diagnostic dilemmas. Therefore, this condition should be treated interdisciplinary. We present a case of a 40-year-old patient with a diagnosis of PG, which in the early stages of the disease was treated as an extensive phlegmon by physicians of other specialties and it presented a serious diagnostic as well as therapeutic problem.
坏疽性脓皮病(PG)是一种相对罕见的嗜中性皮肤病,其特征为进行性皮肤坏死。它通常病程慢性,病因不明。坏疽性脓皮病的诊断可能很困难,因为组织病理学检查和其他实验室检查结果均不具有特异性,而临床状况才是决定性的,对其他医生而言,这会带来许多诊断难题。因此,这种疾病应采用多学科治疗。我们报告一例40岁诊断为PG的患者,在疾病早期,其他专科医生将其当作广泛蜂窝织炎治疗,这带来了严重的诊断及治疗问题。