Vitturi Bruno Kusznir, Frias Amanda, Sementilli Raphael, Racy Marcelo de Castro Jorge, Caffaro Roberto Augusto, Pozzan Geanete
Santa Casa de São Paulo, Faculdade de Ciências Médicas. São Paulo, SP, Brazil.
Santa Casa de São Paulo, Faculdade de Ciências Médicas, Department of Pathology. São Paulo, SP, Brazil.
Autops Case Rep. 2017 Jun 30;7(2):27-34. doi: 10.4322/acr.2017.015. eCollection 2017 Apr-Jun.
Firstly described in the 19th century by Sir William Osler, the mycotic aneurysm (MA) is a rare entity characterized by an abnormal arterial dilation, which is potentially fatal, and is associated with the infection of the vascular wall. Elderly patients are mostly involved, especially when risk factors like chronic diseases, immunosuppression, neoplasia, and arterial manipulation are associated. The authors report the case of a young male patient diagnosed with an aortic aneurysm of infectious origin in the presence of repeated negative blood cultures. The diagnostic hypothesis was raised when the patient was hospitalized for an inguinal hernia surgery. The diagnosis was confirmed based on imaging findings consistent with mycotic aneurism. The patient was treated with an endovascular prosthesis associated with a long-lasting antibiotic therapy. Five months later, the patient attended the emergency unit presenting an upper digestive hemorrhage and shock, from which he died. The autopsy revealed a huge aneurysm of the abdominal aorta with an aortoduodenal fistula. The histological examination of the arterial wall revealed a marked inflammatory process, extensive destruction of the arterial wall, and the presence of Gram-positive bacteria. This case highlights the atypical presentation of a MA associated with an aortoduodenal fistula. Besides the early age of the patient, no primary arterial disease could be found, and no source of infection was detected.
霉菌性动脉瘤(MA)最早于19世纪由威廉·奥斯勒爵士描述,是一种罕见的疾病,其特征为动脉异常扩张,有潜在致命风险,且与血管壁感染有关。老年患者居多,尤其是伴有慢性病、免疫抑制、肿瘤及动脉操作等危险因素时。作者报告了一例年轻男性患者,在多次血培养阴性的情况下被诊断为感染性主动脉瘤。该患者因腹股沟疝手术住院时,诊断假说被提出。基于与霉菌性动脉瘤相符的影像学表现确诊。患者接受了血管内假体治疗并辅以长期抗生素治疗。五个月后,患者因上消化道出血和休克就诊于急诊科,最终死亡。尸检发现腹主动脉巨大动脉瘤并伴有主动脉十二指肠瘘。动脉壁组织学检查显示有明显炎症过程、动脉壁广泛破坏以及革兰氏阳性菌存在。该病例突出了与主动脉十二指肠瘘相关的霉菌性动脉瘤的非典型表现。除患者年龄较轻外,未发现原发性动脉疾病,也未检测到感染源。