阴茎内翻阴道成形术后的术后脓皮病:病例与诊断和管理策略回顾。

Eplasty Pub Date : 2024-05-23 eCollection Date: 2024-01-01
Michael M Talanker, Jessica R Nye, David T Mitchell, Daniel J Freet
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引用次数: 0

摘要

背景:手术后脓皮病(PSPG)是一种非常罕见且难以预测的伤口愈合并发症。切口处溃疡的快速发展可导致不受约束的开裂。PSPG 最常见于乳房手术,但在本研究中,我们详细介绍了一例阴茎内翻阴道成形术后 10 天出现 PSPG 的患者:本例患者按照标准方式接受了阴茎内翻阴道成形术和睾丸切除术。她没有 PSPG 的危险因素。住院期间并无大碍,但术后第 10 天患者出现疼痛难以控制、血清引流增多等症状。再次入院时,发现患者会阴伤口边缘出现大面积轻度化脓性溃疡。在麻醉状态下进行检查时,发现新阴道口通畅完好。切口开裂的部分保持开放,并用乙醇铋敷料重新包扎。由于怀疑是 PSPG,患者立即就诊于皮肤科。患者开始接受为期 18 天的强的松减量治疗,同时使用环孢素以及强力霉素和环丙沙星:免疫抑制治疗 5 天后,溃疡明显转变为健康的肉芽组织,不再活跃化脓。再次冲洗后,已开裂的伤口边缘重新接近。随访时,患者没有 PSPG 复发的迹象,并继续按计划扩张。我们的患者从 PSPG 中康复,没有出现其他并发症,美观效果令人满意:这个独特的病例强调了在怀疑有 PSPG 的情况下及时进行皮肤科会诊、免疫抑制和避免进一步拍片的重要性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Postsurgical Pyoderma Gangrenosum After Penile Inversion Vaginoplasty: Case With Review of Diagnostic and Management Strategies.

Background: Postsurgical pyoderma gangrenosum (PSPG) is a highly uncommon and unpredictable wound healing complication. Rapid progression of ulcers at incisions can cause unfettered dehiscence. Most commonly, PSPG involves breast procedures; however, in this work, we detail a case of a patient who developed PSPG 10 days postoperatively after penile inversion vaginoplasty.

Methods: The patient in this case underwent a penile inversion vaginoplasty with orchiectomy in the standard fashion. She had no risk factors for PSPG. Following an uncomplicated hospital stay, the patient developed difficulty with pain control and increasing serous drainage on the 10th postoperative day. On readmission, the patient was found to have developed large, mildly purulent ulcers throughout the perineal wound edges. On exam under anesthesia, the neovaginal canal was found to be patent and intact. The dehisced portions of the incisions were left open and redressed with occlusive bismuth-petrolatum dressing. Dermatology was promptly consulted with suspicion for PSPG. The patient was started on an 18-day prednisone taper with cyclosporine, along with doxycycline and ciprofloxacin.

Results: After 5 days of immunosuppressive treatment, the ulcers visibly converted to healthy granulation tissue and were no longer actively purulent. Following another washout, the dehisced wound edges were reapproximated. At follow-up, the patient had no evidence of PSPG recurrence and continued dilating on schedule. Our patient recovered from PSPG without further complications and a satisfactory aesthetic result.

Conclusions: This unique case highlights the importance of prompt dermatological consultation, immunosuppression, and avoidance of further pathergy in the setting of suspicion for PSPG.

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