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伴有肛门癌的福尼埃坏疽:一例报告及文献综述

Fournier's gangrene with anal cancer: a case report and literature review.

作者信息

Lee Yunmin, Kim Kyeongeui, Park Chanhee, Lee Jeongwoo, Bae Sunguk, Baek Seongkyu, Jeong Woonkyung

机构信息

Department of Surgery, Keimyung University Dongsan Medical Center, 1035 Dalgubeol-daero, Dalseo-gu, Daegu, 42601, Republic of Korea.

Department of Surgery, Armed Forces Yangju Hospital, 483 Pyeonghwa-ro, Yangju-si, Gyeonggi-do, 11430, Republic of Korea.

出版信息

J Surg Case Rep. 2025 Aug 12;2025(8):rjaf573. doi: 10.1093/jscr/rjaf573. eCollection 2025 Aug.

Abstract

Fournier's gangrene (FG) is a rapidly progressing necrotizing fasciitis affecting the perineum and perianal area, often necessitating urgent surgical intervention. While commonly associated with diabetes, immunosuppression, and infections, malignancy-related FG is uncommon. A 59-year-old female presented with severe left buttock pain and perianal erythema. Imaging studies revealed perineal abscess formation and severe emphysema, leading to a diagnosis of FG. Despite initial surgical debridement and intensive care, persistent perianal induration prompted a biopsy, which confirmed squamous cell carcinoma with HPV 16 positivity. Chemoradiotherapy was administered, achieving significant regression of the tumor and lymph nodes. Robotic abdominoperineal resection was subsequently performed, achieving complete tumor regression (ypT0N0). The patient recovered well initially, but systemic recurrence occurred 10 months after surgery. This case illustrates the infrequent coexistence of FG and anal cancer, highlighting the necessity for early malignancy evaluation in patients with FG.

摘要

福尼尔坏疽(FG)是一种迅速进展的坏死性筋膜炎,累及会阴和肛周区域,常常需要紧急手术干预。虽然FG通常与糖尿病、免疫抑制及感染相关,但与恶性肿瘤相关的FG并不常见。一名59岁女性因左侧臀部剧痛及肛周红斑就诊。影像学检查显示会阴脓肿形成及严重气肿,诊断为FG。尽管初期进行了手术清创及重症监护,但肛周持续硬结促使进行活检,结果证实为HPV 16阳性的鳞状细胞癌。给予放化疗后,肿瘤及淋巴结显著消退。随后进行了机器人辅助腹会阴切除术,实现了肿瘤完全消退(ypT0N0)。患者最初恢复良好,但术后10个月出现全身复发。该病例说明了FG与肛管癌罕见的共存情况,凸显了对FG患者进行早期恶性肿瘤评估的必要性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5eef/12343007/eedb9110da23/rjaf573f1.jpg

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