PDF(Pubmed)
Abstract：
Pyoderma gangrenosum (PG) is a rare and persistent neutrophilic dermatosis with an unknown cause. The condition typically manifests clinically as a pustule or plaque that quickly evolves into a necrotic ulcer with undermined violet-colored margins. A surgical debridement might worsen the disease due to the pathergy phenomenon. This case report presents a 48-year-old woman who underwent a late breast reconstruction with a transverse rectus abdominis myocutaneous flap and was subsequently diagnosed with PG. The report details the delays in the diagnosis and management of the disease, providing a comprehensive account of the course of events.
摘要：
坏疽性脓皮病（PG）是一种罕见且持续的中性粒细胞性皮肤病，原因不明。这种情况通常在临床上表现为脓疱或斑块，迅速演变为坏死性溃疡，紫色边缘受损。手术清创术可能会由于动脉粥样硬化现象而使疾病恶化。该病例报告介绍了一名48岁的妇女，该妇女接受了腹直肌肌皮瓣的晚期乳房重建，随后被诊断为PG。该报告详细介绍了该疾病的诊断和管理方面的延误，提供事件过程的全面描述。
