Song Ethan Y, Wallace Sean J, Teixeira Robert M, Mansour Ahmed, Naktin Jaan P, Miles Marshall, Low Yee Cheng, Wojcik Randolph
University of South Florida Morsani College of Medicine, Tampa, Fla.
Department of Surgery - Division of Plastic and Reconstructive Surgery, Lehigh Valley Health Network, Allentown, Pa.
Plast Reconstr Surg Glob Open. 2020 Nov 20;8(11):e3223. doi: 10.1097/GOX.0000000000003223. eCollection 2020 Nov.
Pyoderma gangrenosum (PG) is a rare and painful inflammatory skin disorder that has been recently associated with breast surgery. It is commonly mistaken for postoperative ischemia or wound infection and does not show response to antibiotics or debridement. We describe the first case of post-surgical PG (PSPG) after alloplastic breast reconstruction involving fat grafting. A 47-year-old woman underwent bilateral mastectomy and 2-stage alloplastic breast reconstruction, with fat grafting from the abdomen. Two days post-surgery, she developed bilateral erythema with tender grouped pustules that progressed rapidly into necrotic ulcerations. She did not respond to antibiotics and serial debridement. Subsequent biopsy confirmed a diagnosis of PG. She was started on steroid therapy and responded well. She was discharged on a steroid regimen, local wound care, and eventually a T-cell inhibitor. Over the next 12 months, her wounds healed without surgical intervention. PSPG has been observed in a variety of reconstructive breast surgeries, but never reported in the setting of fat grafting. As PG involves subcutaneous fat, fat grafting may accelerate and exacerbate the course of disease. Treatment for PSPG includes systemic steroid therapy or other immunomodulatory agents (or both). Surgical management remains controversial, as serial debridement and reconstruction have shown to exacerbate and stimulate disease progression. A long-term follow-up is recommended to monitor for wound healing. Delayed diagnosis of PG in breast reconstruction patients can lead to severe morbidity and disfigurement. This is first case of PSPG following fat grafting in the literature.
坏疽性脓皮病(PG)是一种罕见且疼痛的炎症性皮肤病,最近被发现与乳房手术有关。它常被误诊为术后缺血或伤口感染,对抗生素或清创治疗无反应。我们描述了首例在进行包含脂肪移植的乳房假体再造术后发生的手术后坏疽性脓皮病(PSPG)。一名47岁女性接受了双侧乳房切除术和两阶段乳房假体再造术,并从腹部进行了脂肪移植。术后两天,她出现双侧红斑,伴有触痛性成簇脓疱,迅速发展为坏死性溃疡。她对抗生素和系列清创治疗均无反应。随后的活检确诊为PG。她开始接受类固醇治疗,反应良好。她出院时采用类固醇治疗方案、局部伤口护理,最终使用了一种T细胞抑制剂。在接下来的12个月里,她的伤口未经手术干预就愈合了。PSPG在各种乳房重建手术中均有观察到,但从未有在脂肪移植情况下的报道。由于PG累及皮下脂肪,脂肪移植可能会加速并加重疾病进程。PSPG的治疗包括全身类固醇治疗或其他免疫调节药物(或两者并用)。手术管理仍存在争议,因为系列清创和重建已显示会加重并刺激疾病进展。建议进行长期随访以监测伤口愈合情况。乳房重建患者中PG的延迟诊断可导致严重的发病率和毁容。这是文献中首例脂肪移植后发生的PSPG。