Case Reports in Infectious Diseases

Case Reports in Infectious Diseases / 2019 / Article

Case Report | Open Access

Volume 2019 |Article ID 4939452 | 3 pages |

Descending Thoracic Aortic Aneurysm due to Brucella melitensis

Academic Editor: Jean-François Faucher
Received26 Jan 2019
Accepted14 Aug 2019
Published25 Sep 2019


Brucellosis is an endemic infection mainly in the Middle East and the Mediterranean region that can involve any system. However, cardiovascular involvement commonly seen as endocarditis is a rare occurrence, but it is one of the main causes of mortality and morbidity. Brucella mycotic aneurysms are extremely rare and carry a higher morbidity and mortality. Here, we present a case of Brucella mycotic aneurysms in the descending aorta complicated by an aortoesophageal fistula in a 52-year-old diabetic man. The diagnosis was made by thoracic CT angiogram showing a saccular aneurysm arising from the descending aorta and two positive cultures of Brucella melitensis. Transthoracic and transesophageal echocardiograms ruled out infective endocarditis. Aortoesophageal fistula complicating a Brucella mycotic aneurysm in the absence of evidence of endocarditis has not yet been reported in the literature.

1. Introduction

Brucellosis is a zoonotic disease found more commonly in endemic areas (Middle East and Mediterranean regions) that can affect virtually any system in the human body. However, cardiovascular complications are a rare occurrence, infective endocarditis (IE) being the most common presentation. A meta-analysis was done in Turkey, evaluating 4204 brucellosis patients reported IE in 1.2% of cases [1]. Furthermore, aortic mycotic aneurysm due to Brucella melitensis is a much rarer condition, a review of literature identified cases [2]. To our knowledge, an aortoesophageal fistula complicating a Brucella mycotic aneurysm has not yet been reported in the literature.

2. Case Description

A 52-year-old male, with long-standing type 2 diabetes mellitus, presented to our emergency department (ED) with a history of central, dull chest pain radiating to the back. He complained of intermittent high-grade fever, chills, rigors, sweating, unintentional weight loss, and dysphagia for three months. History was positive for raw milk ingestion and animal contact. Vitals revealed a temperature of 39.1°C; physical exam was unremarkable. Admission laboratory data showed white blood cells 10 (10e9/L), hemoglobin (16.1 mg/dl), platelet count 350 (10e9/L), C-reactive protein 28.5 (mg/dl), and normal electrolytes and coagulation profile. Thoracic CT angiogram demonstrated a saccular aneurysm arising from the descending aorta, distal to origin of the left subclavian artery, with perianeurysmal hematoma compressing the carina, main bronchi, and esophagus (Figure 1). Two sets of blood cultures were positive for Brucella melitensis. Transthoracic and transesophageal echocardiograms ruled out IE. Brucella mycotic aneurysm was diagnosed; appropriate intravenous and oral antibiotics (rifampin and doxycycline) were initiated. During hospitalization, the patient developed massive hematemesis necessitating transfusion of six units packed red blood cells. Angiography exhibited an aortoesophageal fistula (Figure 2), and urgent endovascular repair of the aneurysm was done (Figure 3). Subsequent angiography demonstrated satisfactory stent position with no endovascular leak. The patient received intravenous gentamicin for sixteen days along with rifampin and doxycycline. Upon discharge, rifampin and doxycycline were continued in an oral form for a total of six months. He returned to ED with recurrent hematemesis. CT and conventional angiography revealed no endovascular leak. The patient was discharged home. He again revisited with massive hematemesis with a hemoglobin drop, but no endovascular leak was found on imaging. Blood transfusions were given. Vascular surgeons decided to re-stent, as the thoracic surgeon deemed patient unsuitable for invasive surgical intervention for the aortoesophageal fistula. Esophageal stenting was done (Figure 4), but the patient could not tolerate oral intake, requiring stent removal. The following day the patient became unstable, arrested, and died.

3. Discussion

Brucellosis is a common zoonotic disease worldwide, Brucella melitensis being the most frequent organism [3, 4]. Transmission occurs after ingestion of unpasteurized dairy products and contaminated meat [3]. Brucellosis can present with a variety of clinical manifestations and virtually affecting any system [5]. Aortic brucellosis has an insidious and nonspecific presentation, requiring a high index of suspicion. Any acute pain, whether chest or abdominal with accompanying fever should raise suspicion of aortic involvement. However, there is very scarce information on the presentation patterns, appropriate investigation, and treatment of aortic brucellosis.

Furthermore, mycotic aneurysmal involvement happens due to either direct extension of an adjacent soft tissue infection or embolization of an infectious source. It is thought that in cases of embolization, the emboli reach the adventitia through the vasa vasorum and the inflammation disrupts both the muscularis and adventitia, resulting in blood vessel wall weakness [6]. Human brucellosis requires prolonged periods of multiple antibiotic therapies to completely treat the infection. In cases of cardiovascular complications, treatment becomes more difficult resulting in significant morbidity and mortality [7]. Medical treatment alone has shown to increase mortality rates (33%) when compared to both surgical and medical intervention [811]. Most successfully managed cases were treated with the combination of both medical and surgical intervention [8, 12, 13]. However, treatment of Brucella aortitis and its complications has not been well-established due to the low number of reported cases.

4. Conclusion

Mycotic aneurysm of the aorta due to Brucella is a rare and dangerous complication that needs a high index of suspicion to diagnose. When complicated with an aortoesophageal fistula, it becomes a fatal disease that requires aggressive medical and surgical intervention.


The case report was presented in 5th Scientific Conference of Higher Education Students of King Saud bin Abdulaziz University for Health Sciences (KSAU-HS), Riyadh, Saudi Arabia.

Conflicts of Interest

The authors declare that there are no conflicts of interest regarding the publication of this paper.

Authors’ Contributions

Mohammed Alsheef, Nahar Alanezi, and Arshad Mian revised the manuscript and approved the final version. Saud Alsaleh, Nizar bakhsh, Rana AlDosary, and Lina AlSharif retrieved the study information and drafted the manuscript. Azim Ahsan revised the manuscript in term of proper management of antibiotic course and approved the final version. Isamme AlFayyad drafted the manuscript, proofread, and approved the final version.


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Copyright © 2019 Mohammed Alsheef et al. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

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