Amor Imed Ben, Kassir Radwan, Bachir Elias, Katharina Hufschmidt, Debs Tarek, Gugenheim Jean
Department of General Surgery, Archet 2 Hospital, University Hospital of Nice, Nice, France.
Department of General Surgery, CHU Hospital, Jean Monnet University, Avenue Albert Raimond 42270, Saint Etienne, France.
Int J Surg Case Rep. 2015;8C:73-5. doi: 10.1016/j.ijscr.2014.12.034. Epub 2015 Jan 8.
Diverticular disease of the colon is a frequent pathology; however, perforated diverticulitis with a spontaneous sigmoidocutaneous fistula revealed by a perianal abscess is an uncommon presentation. We present this extremely rare case of a perforated sigmoid diverticulum in the perianal area, which is the first case that we have encountered in our practice and in the literature, along with the accompanying diagnostic and therapeutic issues and a review of the literature.
We report the case of a 47-year-old man who was admitted to the emergency room due to a perianal abscess. The patient was taken to the operating room on an emergency basis. In the lithotomy position, the abscess was located at the 4 o'clock position. Incision and drainage was performed. Intraoperatively, the abscess was found to be deep, and considered an ischiorectal abscess. No fistulous tract was identified. An MRI of the pelvis was performed one month postoperatively which revealed a perforated diverticulitis of the sigmoid colon causing a perianal fistula. After the abscess was successfully treated, a sigmoidectomy was performed. Fifteen centimeters of the colon were resected. No postoperative complications occurred.
Perianal fistula is an obvious physical sign but its etiology is complex to determine. The pathophysiological mechanism involved is the emergence of a pressure gradient between the peritoneum and surrounding structures, causing rupture of the perianal tissue, allowing gas from a perforation to diffuse along tissue planes.
General surgeons should bear in mind this rare presentation of a sigmoid diverticulitis.
结肠憩室病是一种常见的病理状况;然而,由肛周脓肿揭示的伴有自发性乙状结肠皮肤瘘的穿孔性憩室炎是一种不常见的表现。我们呈现这例极其罕见的肛周区域乙状结肠穿孔病例,这是我们在临床实践及文献中首次遇到的病例,同时还介绍了相关的诊断和治疗问题并对文献进行综述。
我们报告一例47岁男性患者,因肛周脓肿入住急诊室。患者紧急被送往手术室。在截石位时,脓肿位于4点钟位置。进行了切开引流。术中发现脓肿较深,考虑为坐骨直肠窝脓肿。未发现瘘管。术后一个月进行了骨盆MRI检查,结果显示乙状结肠穿孔性憩室炎导致肛周瘘管形成。脓肿成功治疗后,进行了乙状结肠切除术。切除了15厘米的结肠。未发生术后并发症。
肛周瘘管是一个明显的体征,但其病因难以确定。涉及的病理生理机制是腹膜与周围结构之间出现压力梯度,导致肛周组织破裂,使穿孔处的气体沿组织平面扩散。
普通外科医生应牢记这种罕见的乙状结肠憩室炎表现。