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Primary Aortoduodenal Fistula

机译:原发性十二指肠瘘

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Primary aortoduodenal fistula is a rare cause of gastrointestinal bleeding that is difficult to diagnose. A “herald” bleed often precedes fatal hemorrhage. Endoscopy, ultrasound, angiography and CT scan have all been utilized in an attempt to confirm this diagnosis with limited success. We report a 51-year-old male who presented with occasional melanotic stools, and then developed massive upper gastrointestinal bleeding. A primary aortoduodenal fistula was identified between an atherosclerotic abdominal aortic aneurysm, and the third portion of the duodenum in surgery. The aneurysm was resected and grafted and the duodenum repaired. The patient developed a severe coagulopathy and expired post-operatively. This case illustrates a rare presentation of both abdominal aortic aneurysm and gastrointestinal bleeding. We will discuss the challenges in diagnosis and management of this unusual problem. Introduction Primary aortoduodenal fistula (PADF) is a communication between the aorta and the enteric tract without any previous vascular intervention, e.g., aortic grafting. Although rare, PADF is a lethal condition that requires a high index of suspicion. Delay in diagnosis and treatment has been historically associated with extremely high mortality .We present a case of PADF due to an abdominal aortic aneurysm. Diagnosis was made at surgical exploration. Despite the use of angiography, and repeated computed tomography (CT) scans, the diagnosis of a PADF secondary to an abdominal aortic aneurysm is often difficult to make, leading to a delay in diagnosis until the time of surgery [2]. This extremely rare condition requires a high index of clinical suspicion even in a patient with undiagnosed aortic disease. Case Report A 51-year old male presented to the emergency room with a chief complaint of rectal bleeding. The patient reported intermittent bleeding for one year which had worsened over the past two days. He also reported feeling “dizzy” with occasional bright red blood per rectum.PMH was significant for hypertension, non-insulin dependent diabetes, peptic ulcer disease, GERD, and osteomyelitis of his cervical spine. No surgical history. Current medications included Glucophage, Lipitor, and Lisinopril. No history of drug, alcohol or tobacco use. Review of systems was otherwise non-contributory.The patient appeared in mild distress, was well hydrated, alert and oriented heart rate 108, blood pressure 106/61 with no orthostatic changes. Pulses were palpable at 2+ throughout. Abdomen was soft and mildly tender in the epigastrium. Rectal exam revealed gross blood.Lab work was unremarkable except for hemoglobin of 11g/dl and BUN/Cr 33/l.4. A nasogastric tube was placed. His stomach was lavaged with no blood. The patient was admitted with the diagnosis of GI bleeding of unknown etiology. EGD was performed which showed mild gastritis and duodenitis but no bleeding. Two days later the patient passed another 500ml of melana, received two units of PRBC and underwent colonoscopy which was unremarkable. His bleeding stopped and a subsequent barium small bowel study failed to show a mass or lesion. Plans were made for CT/ angiogram.Day six after admission, the patient had abdominal pain, a large upper GI bleed and melena. Repeat EGD showed a large clot in the third portion of the duodenum. Exploratory laparotomy revealed a communication between the aorta and third portion of the duodenum. The aneurysm was resected and grafted and the duodenum repaired. Unfortunately, the patient developed severe coagulopathy and expired six hours postoperatively. Discussion The most common site of aortoenteric fistulization is at the third portion of the duodenum because of its fixed retroperitoneal location overlying the aorta. While this condition is extremely rare with an incidence rate at autopsy of 0.04 to 0.07%, secondary ADF occurs much more commonly (post-operative incidence -0.5 to 2.3%), and is due to prior aortic surgery and/or the placement of a synt
机译:原发性主动脉十二指肠瘘是胃肠道出血的罕见原因,难以诊断。致命出血通常先于“先驱”出血。内窥镜检查,超声检查,血管造影检查和CT扫描均已被用于尝试以有限的成功率来证实该诊断。我们报告了一名51岁的男性,偶尔出现黑色素粪便,然后出现大量上消化道出血。在手术中,在动脉粥样硬化腹主动脉瘤与十二指肠第三部分之间发现了原发性主动脉十二指肠瘘。切除和移植动脉瘤并修复十二指肠。该患者出现严重的凝血病,术后死亡。该病例说明了腹部主动脉瘤和胃肠道出血的罕见表现。我们将讨论此异常问题在诊断和管理方面的挑战。简介主动脉十二指肠瘘(PADF)是主动脉与肠道之间的连通,而无需任何先前的血管干预,例如主动脉移植。尽管很少见,但PADF是一种致命疾病,需要高度怀疑。历史上,诊断和治疗的延迟一直与极高的死亡率相关。我们目前由于腹主动脉瘤而导致PADF病例。在手术探查时进行诊断。尽管使用了血管造影术和重复的计算机断层扫描(CT)扫描,腹主动脉瘤继发的PADF的诊断通常还是很困难,导致诊断延迟到手术时间[2]。即使在患有未确诊的主动脉疾病的患者中,这种极为罕见的疾病也需要高度的临床怀疑。病例报告一名51岁的男性因直肠出血而主诉急诊室。该患者报告了一年的间歇性出血,在过去两天内恶化了。他还报告说感到“头晕”,偶尔每个直肠有鲜红色的血液。PMH对高血压,非胰岛素依赖型糖尿病,消化性溃疡疾病,GERD和颈椎骨髓炎很重要。无手术史。当前的药物包括Glucophage,Lipitor和Lisinopril。没有药物,酒精或烟草使用史。否则,系统检查无贡献。患者出现轻度不适,身体水分充足,心律敏锐,定向心律108,血压106/61,无立位性改变。整个脉搏可触及2+。腹部柔软,上腹部轻柔。直肠检查发现血液量大,除血红蛋白为11g / dl和BUN / Cr 33 / l.4外,实验室工作无异常。放置鼻胃管。他的肚子没血了。该患者被确诊为病因不明的胃肠道出血。进行的EGD表现为轻度胃炎和十二指肠炎,但无出血。两天后,患者又通过了500毫升的黑色素,接受了两单位PRBC的治疗,并接受了结肠镜检查。他的出血停止了,随后进行的钡小肠检查未能显示肿块或病变。计划进行CT /血管造影。入院后第六天,患者出现腹痛,上消化道大出血和黑斑。重复EGD显示十二指肠第三部分有大血块。探索性剖腹术揭示了主动脉和十二指肠第三部分之间的连通。切除和移植动脉瘤并修复十二指肠。不幸的是,患者出现了严重的凝血病,术后六个小时死亡。讨论由于十二指肠的固定腹膜后位置覆盖主动脉,因此最常见的主动脉瘘部位是十二指肠的第三部分。虽然这种情况极为罕见,尸检时的发生率为0.04至0.07%,但继发性ADF的发生率更高(术后发生率-0.5至2.3%),这是由于先前的主动脉手术和/或放置了ADF而引起的。句法

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