Spontaneous colocutaneous diverticular fistula presenting as perianal abscessA 76-year-old man presented with a recurrent perianal abscess, following 1 month of diarrhoea, perianal pain and reduced appetite. Absence of an anal fistula and the high extent of the abscess cavity prompted a magnetic resonance imaging scan, which demonstrated a tract extending from sigmoid colon to the ischioanal abscess. Colonoscopy was performed to confirm diverticular disease and exclude malignancy. The patient underwent an elective laparoscopic-assisted anterior resection and temporary defunctioning loop ileostomy.Bilateral ureteric stents were inserted due to hydronephrosis from left ureteric obstruction and to assist intraoperative identification of ureters. Laparoscopic mobilization of the splenic flexure was undertaken first. Dissection of the sigmoid colon and mesorectum was difficult due to surrounding fibrosis and residual purulent inflammation, and was performed through a lower midline incision. Subsequent resection, anastomosis and loop ileostomy proceeded uneventfully. The patient was discharged on post-operative day 16, having had issues with high stoma output.Diverticular colocutaneous fistulae are rare, and usually follow operation or percutaneous drainage of diverticular abscesses. Spontaneous diverticular colocutaneous fistulae, especially to the perineum are even rarer, with only four cases found in the literature since 2000. [1][2][3][4] Elective operations for diverticular fistulae are usually difficult. They are often performed open due to issues with abdominal access and difficulties identifying dissection planes. In our case, laparoscopic mobilization of the splenic flexure reduced the required extent of the midline wound. Ureteric stents were vital to preservation of the ureters while dissecting out the fistula, and for treatment of the hydronephrosis.Spontaneous colocutaneous diverticular fistula presenting with perianal abscess is exceedingly rare. An intra-abdominal source of sepsis should be considered in recurrent perianal abscess without anal fistula. Anticipation of a difficult dissection should prompt consideration of ureteric stents, but a laparoscopic approach, at least initially, is feasible. References 1. Amor IB, Kassir R, Bachir E, Katharina H, Debs T, Gugenheim J. Perforated diverticulitis of the sigmoid colon revealed by a perianal fistula. Int. J. Surg. Case Rep. 2015; 8c: 73-5. 2. Chadwick T, Katti A, Arthur J. Sigmoid-gluteal fistula: a rare complication of fistulating diverticular disease. J. Surg. Case Rep. 2017; 2017: rjw237. 3. Evaristo-Mendez G, Sanchez-Hernandez AT, Melo-Velazquez A, Ventura-Sauceda FA, Sepulveda-Castro RR. Sigmoido-buttock fistula by diverticulitis: report of a rare complication. Cir. Cir. 2013; 81: 158-62. 4. Fehmer T, Citak M, Schildhauer TA. Sigmoido-gluteal fistulaa rare complication in clinically asymptomatic chronic diverticulitis. Acta Chir.