Cuijpers Anne C M, de Boer Sanne W, van der Leij Christiaan, Coolsen Marielle M E
Department of Surgery, Maastricht University Medical Centre, PO Box 5800, 6202 AZ Maastricht, the Netherlands.
Department of Radiology, Maastricht University Medical Centre, PO Box 5800, 6202 AZ Maastricht, the Netherlands.
Int J Surg Case Rep. 2021 Feb;79:331-334. doi: 10.1016/j.ijscr.2021.01.064. Epub 2021 Jan 20.
Mycotic aneurysms are a severe and sometimes life-threatening complication of infections or sepsis. However, mycotic aneurysms of mesenteric arteries caused by a purulent peritonitis following perforated appendicitis are very rare and not previously reported. This case report contributes to the awareness and treatment of this rare complication.
We present a case of a middle aged patient with a purulent peritonitis after perforated appendicitis. Postoperatively, recovery was not as expected. One week after laparoscopic appendectomy, CRP increased and haemoglobin levels dropped. Abdominal CT imaging revealed several mesenteric mycotic aneurysms. Because of aneurysmatic rupture, coiling of several mesenteric arteries was performed, despite the risk of bowel ischemia. After long-term antibacterial and antifungal treatment, the patient recovered completely.
Formation of mycotic aneurysms in mesenteric arteries is very rare and optimal treatment options are debatable. Given the high mortality of conservative therapy with antibiotics alone, treatment of mycotic aneurysms by surgery or endovascular treatment is strongly advised. In our case, it was decided to treat the aneurysms by endovascular coil embolization and to observe whether bowel ischemia would occur, because aneurysms were present in multiple mesenteric arteries.
Mycotic aneurysms of several mesenteric arteries should be considered as a rare but potential complication of perforated appendicitis with purulent peritonitis. In case of rupture, successful treatment can be achieved by embolization followed by long-term antibiotics. A multidisciplinary approach including surgery, interventional radiology and microbiology is highly recommended and transfer to a tertiary referral centre should be considered.
真菌性动脉瘤是感染或脓毒症的一种严重且有时危及生命的并发症。然而,由穿孔性阑尾炎后脓性腹膜炎引起的肠系膜动脉真菌性动脉瘤非常罕见,此前未见报道。本病例报告有助于提高对这种罕见并发症的认识和治疗。
我们报告一例中年患者,穿孔性阑尾炎后发生脓性腹膜炎。术后恢复未达预期。腹腔镜阑尾切除术后一周,CRP升高,血红蛋白水平下降。腹部CT成像显示多个肠系膜真菌性动脉瘤。由于动脉瘤破裂,尽管存在肠缺血风险,仍对多条肠系膜动脉进行了栓塞治疗。经过长期抗菌和抗真菌治疗,患者完全康复。
肠系膜动脉真菌性动脉瘤的形成非常罕见,最佳治疗方案存在争议。鉴于单独使用抗生素进行保守治疗的高死亡率,强烈建议通过手术或血管内治疗真菌性动脉瘤。在我们的病例中,决定通过血管内线圈栓塞治疗动脉瘤,并观察是否会发生肠缺血,因为多个肠系膜动脉存在动脉瘤。
多条肠系膜动脉真菌性动脉瘤应被视为穿孔性阑尾炎合并脓性腹膜炎的一种罕见但潜在的并发症。一旦破裂,可通过栓塞治疗,随后长期使用抗生素实现成功治疗。强烈建议采用包括外科手术、介入放射学和微生物学在内的多学科方法,并应考虑转诊至三级转诊中心。