小儿罕见部位坏疽性脓皮病1例:病例报告及文献复习

Z. Mehsas, S. Sektaoui, B. Boubnane, M. Meziane, N. Ismaili, L. Benzekri, K. Senouci
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引用次数: 0

摘要

一个12岁的女孩,她的脸上有三个溃疡病变,红色,肿胀,边缘向前推进,破坏。尽管进行了静脉注射和局部抗生素治疗,溃疡并没有改善,培养也没有显示出微生物的生长。患者没有任何潜在的全身性疾病,皮肤活检显示中性粒细胞皮炎。开始口服强的松,导致病变愈合。皮肤活检和皮质类固醇阳性反应证实了坏疽性脓皮病(PG)的诊断。PG是一种罕见的皮肤炎症性疾病,面部病变是罕见的表现。早期开始免疫抑制治疗对于完全愈合和减少显著的心理影响至关重要。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Pyoderma Gangrenosum at Uncommon Site in a Pediatric Patient: Case Report and Review of Literature
A 12-year-old girl presented with three ulcerated lesions on her face that were red, swollen, had advancing borders, and undermined. Despite treatment with intravenous and topical antibiotics, the ulcers did not improve, and cultures showed no growth of organisms. The patient did not have any underlying systemic disease, and a skin biopsy revealed neutrophilic dermatitis. Oral prednisone was started, which resulted in the healing of the lesions. The skin biopsy and positive response to corticosteroids confirmed the diagnosis of Pyoderma Gangrenosum (PG). PG is a rare inflammatory skin condition, and facial lesions are a rare presentation. Early initiation of immunosuppressive therapy is crucial for complete healing and to minimize the significant psychological impact.
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