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DOI: 10.1148/radiol.2311021700
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(Radiology 2004;231:250-257.)
© RSNA, 2004


Vascular and Interventional Radiology

Infected Aortic Aneurysms: Imaging Findings1

Thanila A. Macedo, MD, Anthony W. Stanson, MD, Gustavo S. Oderich, MD, C. Michael Johnson, MD, Jean M. Panneton, MD and Mark L. Tie, MD

1 From the Department of Radiology (T.A.M., A.W.S., C.M.J.) and Division of Vascular Surgery (G.S.O., J.M.P.), Mayo Clinic and Foundation, 200 First St SW, Rochester, MN 55905; and Department of Radiology, Queen Elizabeth Hospital, Woodville, SA, Australia (M.L.T.). Received December 9, 2002; revision requested February 27, 2003; final revision received August 1; accepted August 22. Address correspondence to T.A.M. (e-mail: macedo.thanila@mayo.edu).


    ABSTRACT
 TOP
 ABSTRACT
 INTRODUCTION
 MATERIALS AND METHODS
 RESULTS
 DISCUSSION
 REFERENCES
 
PURPOSE: To determine the imaging characteristics of infected aortic aneurysms.

MATERIALS AND METHODS: Review of records of patients with surgical and/or microbiologic proof of infected aortic aneurysm obtained over a 25-year period revealed 31 aneurysms in 29 patients. This study included 21 men and eight women (mean age, 70 years). One radiologist reviewed 28 computed tomographic (CT) studies (22 patients underwent CT once and three patients underwent CT twice), 12 arteriograms (12 patients underwent arteriography once), eight nuclear medicine studies (six patients underwent nuclear medicine imaging once and one patient underwent nuclear medicine imaging twice), and three magnetic resonance (MR) studies (three patients underwent MR imaging once). Features evaluated included aneurysm size, shape, and location; branch involvement; aortic wall calcification; gas; radiotracer uptake on nuclear medicine studies; and periaortic and associated findings. The location of infected aortic aneurysms was compared with that of arteriosclerotic aneurysms.

RESULTS: Aneurysms were located in the ascending aorta (n = 2, 6%), descending thoracic aorta (n = 7, 23%), thoracoabdominal aorta (n = 6, 19%), paravisceral aorta (n = 2, 6%), juxtarenal aorta (n = 3, 10%), infrarenal aorta (n = 10, 32%), and renal artery (n = 1, 3%). Two patients had two infected aortic aneurysms. CT revealed 25 saccular (93%) and two fusiform (7%) aneurysms with a mean diameter at initial discovery of 5.4 cm (range, 1–11 cm). Paraaortic soft-tissue mass, stranding, and/or fluid was present in 13 (48%) of 27 aneurysms, and early periaortic edema with rapid aneurysm progression and development was present in three (100%) patients with sequential studies. Other findings included adjacent vertebral body destruction with psoas muscle abscess (n = 1, 4%), kidney infarct (n = 1, 4%), absence of calcification in the aortic wall (n = 2, 7%), and periaortic gas (n = 2, 7%). Angiography showed 13 saccular aneurysms with lobulated contour in 10 (77%). Nuclear medicine imaging showed increased activity consistent with infection in six (86%) of seven aneurysms. MR imaging showed three saccular aneurysms. Adjacent abnormal vertebral body marrow signal intensity was seen in one (33%) of three patients.

CONCLUSION: Saccular aneurysms (especially those with lobulated contour) with rapid expansion or development and adjacent mass, stranding, and/or fluid in an unusual location are highly suspicious for an infected aneurysm.

© RSNA, 2004

Index terms: Aneurysm, aortic, 94.733, 981.733 • Aneurysm, CT, 94.12916, 981.12916 • Aneurysm, MR, 94.12942, 981.12942


    INTRODUCTION
 TOP
 ABSTRACT
 INTRODUCTION
 MATERIALS AND METHODS
 RESULTS
 DISCUSSION
 REFERENCES
 
Infected aortic aneurysm was described by Sir William Osler in 1885 (1). It is estimated to represent about 0.7%–2.6% of all aortic aneurysms (2,3). In addition to being rare, infected aneurysms represent a diagnostic and therapeutic challenge. Patients commonly have nonspecific symptoms that may not be detected until aneurysm rupture or late stages of sepsis. Infected aneurysms are prone to rupture, with reports of 53%–75% aneurysm rupture at surgery (36). Prompt recognition of this entity is of paramount importance in the diagnosis and treatment of this disorder and for successful patient outcome.

Diagnostic imaging findings of infected aneurysms have been described mostly in case reports. The largest series come from the surgery literature, but these lack detailed information about radiologic findings. The purpose of this study was to determine the imaging characteristics of infected aortic aneurysms.


    MATERIALS AND METHODS
 TOP
 ABSTRACT
 INTRODUCTION
 MATERIALS AND METHODS
 RESULTS
 DISCUSSION
 REFERENCES
 
Patients
We reviewed data in the radiology and vascular surgery database that was collected over a 25-year period (December 1976–March 2001) and identified 58 patients in whom infected or mycotic aortic aneurysms were diagnosed. These 58 patients represented less than 1% of the 7,274 patients who underwent repair of aortic aneurysms at the Mayo Clinic during this period. Imaging studies were available for 29 patients, who formed our study; 24 of these were part of a cohort from a larger, previously described surgical series (3).

The mean interval between the imaging examination and confirmation of the diagnosis at surgery was 5 days (range, 1–19 days). Infected aortic aneurysm was diagnosed with gross intraoperative findings (inflammation and purulence), clinical evidence of infection (fever, leukocytosis, or both), and aneurysm wall cultures that were positive for infection. Aneurysms in which the culture was negative for infection were analyzed individually. Patients had to have convincing surgical findings, a fever of unknown origin, and had to be using antibiotics before culture samples were collected. We excluded patients with infected aneurysms caused by local complication of prosthetic grafts and patients with infected aneurysms isolated in aortic branches or peripheral locations. Institutional review board approval was obtained, and informed consent was not required for this retrospective study.

Record and Image Review
Demographics, clinical characteristics, and surgical findings were collected from the patient records by either of two authors (G.S.O., T.A.M.). Available imaging studies were reviewed by a vascular radiologist (A.W.S.) with 29 years of experience. Though the reviewer was aware that all the images were of infected aneurysms, he was blinded to the clinical and surgical findings.

The following 51 imaging studies were available for review: 28 computed tomographic (CT) studies (22 patients underwent CT once, three patients underwent CT twice, and four patients did not undergo CT), 12 arteriographic studies (12 patients underwent arteriography once and 17 patients did not undergo arteriography), three magnetic resonance (MR) angiographic studies (three patients underwent MR angiography once and 26 patients did not undergo MR angiography), and eight nuclear medicine studies (six patients underwent nuclear medicine imaging once, one patient underwent nuclear medicine imaging twice, and 22 patients did not undergo nuclear medicine imaging). Multiple studies in a given patient were reviewed at the same time.

Three patients underwent multiple CT examinations within 24–50 days. CT examinations were performed both before and after administration of intravenous contrast material in seven patients, after administration of contrast material in 16 patients, and without contrast material in five patients. The section thickness used for CT was 6–10 mm. Aneurysms were measured on hard-copy film images. Angiograms obtained before 1992 were available in conventional film format, while angiograms obtained after 1992 were obtained with digital subtraction technology. All procedures were performed in at least two views. Nuclear medicine studies included six indium 111 (111In)-tagged white blood cell examinations, one hexamethylpropyleneamine oxime (HMPAO)-tagged white blood cell examination, and one gallium 67 (67Ga) examination. MR imaging and MR angiography were performed with a 1.5-T magnet. Three-dimensional time-of-flight MR angiograms were obtained with gadolinium enhancement in two of three patients, one of whom also underwent transverse T1-weighted MR imaging. One of these three patients underwent transverse T1-weighted MR imaging only.

Features evaluated both on CT and MR studies included aneurysm location, size, and shape (saccular or fusiform); branch involvement; adjacent soft-tissue mass, stranding, and/or fluid; and any additional findings. Calcification in the adjacent or involved aortic wall and presence of gas were evaluated on CT scans only. When consecutive CT studies were available for a given patient, the progression of findings was evaluated, and early subtle edema was defined as stranding in the surrounding fat present on the initial scan.

The location of infected aneurysms was compared with the location of arteriosclerotic aneurysms described in the literature. On conventional arteriograms, the shape of the aneurysm, contour lobulation, branch involvement, measurements, and any additional findings were described. Aneurysm measurements were given as a ratio relative to adjacent aortic diameter. Nuclear medicine scans were evaluated for presence or absence of increased radiotracer uptake. Microbiology of infected aneurysms was correlated with increased radiotracer uptake on nuclear medicine scans, the presence of gas on CT scans, vertebral body changes, multiplicity of aneurysms, and periaortic soft-tissue mass, stranding, and/or fluid.


    RESULTS
 TOP
 ABSTRACT
 INTRODUCTION
 MATERIALS AND METHODS
 RESULTS
 DISCUSSION
 REFERENCES
 
Clinical Characteristics
Our study included 21 men and eight women (mean age, 70 years; range, 37–94 years). Symptoms were present in 26 patients (90%) an average of 36 days (range, 1–220 days). The most common symptoms at presentation were fever in 19 patients and abdominal pain, back pain, or both in 18 patients. Three patients were asymptomatic. The causative organisms were Staphylococcus (n = 8), Escherichia coli (n = 4), Salmonella (n = 4), Streptococcus (n = 3), Listeria (n = 1), and Haemophilus (n = 1). Cultures were negative for infection in eight patients. Erythrocyte sedimentation rates were 19–135 mm/h (mean, 84.5 mm/h) and were elevated (>30 mm/h in women and >22 mm/h in men) in 11 of 12 patients. White blood cell levels were 4.2–25.5 x 109/L (mean, 12.12 x 109/L) and were elevated (>10.5 x 109/L) in 14 of 24 patients. Leukocytosis and an elevated erythrocyte sedimentation rate were present in six patients.

Conventional Angiography
Twelve patients underwent arteriography. In one patient (8%), an arteriogram was negative for aneurysm and a CT study—which was obtained 2 weeks later—was positive for aneurysm. In two (17%) additional patients, two infected aneurysms were found, yielding a total of 13 aneurysms. Aneurysm shape was saccular in 13 (100%) of 13 aneurysms. Contour lobulation was appreciated in 10 (77%) of 13 aneurysms (Fig 1). Vertebral body erosion was noted in one (8%) of 13 aneurysms (Fig 2). On average, the ratio of the aneurysm diameter was increased by a factor of 2.2, and the length was 1.9 times the diameter of the healthy adjacent aorta. In 13 patients, aneurysms were located in the thoracoabdominal aorta (n = 4, 31%), the descending thoracic aorta (n = 3, 23%), the paravisceral aorta (adjacent to the origin of the celiac, superior mesenteric, and renal arteries) (n = 2, 15%), the infrarenal aorta (n = 2, 15%), the juxtarenal aorta (n = 1, 8%), and the renal artery (n = 1, 8%). Branch involvement was present in five (42%) of 12 patients and included the celiac artery (n = 4, 33%), the superior mesenteric artery (n = 3, 25%), and the renal artery (n = 3, 25%) (the sum of percentages is higher than the total because of the combination of branches involved).



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Figure 1a. Images obtained in a 64-year-old woman with infected paravisceral aortic aneurysm. (a) Frontal arteriogram demonstrates characteristic saccular aneurysm (*) with lobulated contour. (b) Coronal 111In white blood cell scan shows increased radiotracer uptake in the region of the aneurysm (arrow) and suggests an infection. (c) Transverse contrast-enhanced CT scan shows a saccular aneurysm (*) with prominent periaortic inflammation and fluid (arrow) measuring 7.5 x 11 cm in diameter.

 


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Figure 1b. Images obtained in a 64-year-old woman with infected paravisceral aortic aneurysm. (a) Frontal arteriogram demonstrates characteristic saccular aneurysm (*) with lobulated contour. (b) Coronal 111In white blood cell scan shows increased radiotracer uptake in the region of the aneurysm (arrow) and suggests an infection. (c) Transverse contrast-enhanced CT scan shows a saccular aneurysm (*) with prominent periaortic inflammation and fluid (arrow) measuring 7.5 x 11 cm in diameter.

 


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Figure 1c. Images obtained in a 64-year-old woman with infected paravisceral aortic aneurysm. (a) Frontal arteriogram demonstrates characteristic saccular aneurysm (*) with lobulated contour. (b) Coronal 111In white blood cell scan shows increased radiotracer uptake in the region of the aneurysm (arrow) and suggests an infection. (c) Transverse contrast-enhanced CT scan shows a saccular aneurysm (*) with prominent periaortic inflammation and fluid (arrow) measuring 7.5 x 11 cm in diameter.

 


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Figure 2a. Images obtained in a 73-year-old man with infected infrarenal aortic aneurysm associated with osteomyelitis and psoas muscle abscess. (a) Transverse contrast-enhanced CT scan shows an infrarenal aortic aneurysm (*) measuring 11 x 6 cm in diameter associated with a left psoas muscle abscess (arrowhead) and vertebral body destruction (arrow). (b) Sagittal T1-weighted MR image shows abnormal signal intensity (arrow) in the bone marrow of the vertebral body.

 


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Figure 2b. Images obtained in a 73-year-old man with infected infrarenal aortic aneurysm associated with osteomyelitis and psoas muscle abscess. (a) Transverse contrast-enhanced CT scan shows an infrarenal aortic aneurysm (*) measuring 11 x 6 cm in diameter associated with a left psoas muscle abscess (arrowhead) and vertebral body destruction (arrow). (b) Sagittal T1-weighted MR image shows abnormal signal intensity (arrow) in the bone marrow of the vertebral body.

 
CT Scanning
Aneurysm shape was saccular in 25 (93%) and fusiform in two (7%) aneurysms. One of the fusiform aneurysms had extensive mural thrombus. Periaortic soft-tissue mass, stranding, and/or fluid were present in 13 (48%) of 27 aneurysms (Fig 1). Early subtle periaortic edema with rapid aneurysm progression and development was noticed in all three patients who underwent sequential examinations. In one patient, a 3.5 x 5.0-cm aneurysm developed during a 7-week interval (Fig 3). In one patient, a 4-cm aneurysm developed during a 23-day interval. In another patient, not only did the periaortic edema increase, but a 4-cm aneurysm also developed within 7 days (Fig 4). Renal infarct, which involved about two-thirds of the left kidney, was present in one (4%) of the 25 patients. Periaortic gas collection was seen in two (7%) of the 27 aneurysms (Fig 5). Vertebral body destruction with psoas muscle abscess was an associated finding in one (4%) of 27 aneurysms (Fig 2). Absence of atheromatous calcification in the aortic wall was noted in two (7%) of 27 aneurysms, while calcification was seen in the aneurysm wall in seven (26%) aneurysms and in the aortic wall adjacent to the aneurysm in the remaining 18 (67%) aneurysms. Aneurysms were located in the ascending aorta (n = 2, 7%), in the descending thoracic aorta (n = 5, 19%), in the thoracoabdominal aorta (n = 6, 22%), in the juxtarenal aorta (n = 2, 7%), in the renal artery (n = 1, 4%), in the paravisceral aorta (n = 2, 7%), and in the infrarenal aorta (n = 9, 33%). Branch involvement was seen in 15 (56%) of 27 aneurysms and included the celiac artery (n = 7, 26%), the superior mesenteric artery (n = 4, 15%), the renal artery (n = 5, 19%), the inferior mesenteric artery (n = 5, 19%), the aortic arch branches (n = 1, 4%), and the coronary artery, with extension into the interventricular septum (n = 1, 4%). The sum of these percentages is greater than 100% because of the combination of branches involved. The average maximum diameter was 5.4 cm (range, 1–11 cm), and the average length was 4.5 cm (range, 1–10 cm).



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Figure 3a. Images obtained in a 56-year-old man with infected thoracoabdominal aortic aneurysm. (a) Transverse contrast-enhanced CT scan shows atherosclerotic changes and loss of the periaortic fat plane (arrow). (b) Transverse contrast-enhanced CT scan obtained 7 weeks later shows that a 3.5 x 5.0-cm saccular aneurysm (arrow) has developed.

 


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Figure 3b. Images obtained in a 56-year-old man with infected thoracoabdominal aortic aneurysm. (a) Transverse contrast-enhanced CT scan shows atherosclerotic changes and loss of the periaortic fat plane (arrow). (b) Transverse contrast-enhanced CT scan obtained 7 weeks later shows that a 3.5 x 5.0-cm saccular aneurysm (arrow) has developed.

 


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Figure 4a. Images obtained in a 69-year-old woman with infected infrarenal aortic aneurysm. (a) Transverse contrast-enhanced CT scan shows subtle periaortic fat stranding (arrow). (b) Transverse contrast-enhanced CT scan obtained 1 week later shows progression of findings. (c) Coronal 111In-labeled white blood cell scan shows intense radiotracer uptake (arrow) in the region of the aneurysm, which is suggestive of an infection. Rapid development and/or size progression is a feature of infected aneurysms.

 


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Figure 4b. Images obtained in a 69-year-old woman with infected infrarenal aortic aneurysm. (a) Transverse contrast-enhanced CT scan shows subtle periaortic fat stranding (arrow). (b) Transverse contrast-enhanced CT scan obtained 1 week later shows progression of findings. (c) Coronal 111In-labeled white blood cell scan shows intense radiotracer uptake (arrow) in the region of the aneurysm, which is suggestive of an infection. Rapid development and/or size progression is a feature of infected aneurysms.

 


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Figure 4c. Images obtained in a 69-year-old woman with infected infrarenal aortic aneurysm. (a) Transverse contrast-enhanced CT scan shows subtle periaortic fat stranding (arrow). (b) Transverse contrast-enhanced CT scan obtained 1 week later shows progression of findings. (c) Coronal 111In-labeled white blood cell scan shows intense radiotracer uptake (arrow) in the region of the aneurysm, which is suggestive of an infection. Rapid development and/or size progression is a feature of infected aneurysms.

 


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Figure 5. CT scan in a 69-year-old man with infected infrarenal aortic aneurysm demonstrates a subtle saccular aneurysm associated with periaortic gas (arrows). The presence of gas is an infrequent finding associated with infected aneurysms.

 
Two patients had two infected aneurysms. One patient had one aneurysm in the infrarenal abdominal aorta and one in the right renal artery. The other patient had one aneurysm in the descending thoracic aorta and one in the paravisceral aorta.

MR Imaging
Three aneurysms were demonstrated with MR imaging, and saccular shape was present in all three. Two aneurysms (66%) were located in the paravisceral aorta and one (33%) was located in the infrarenal aorta. In one aneurysm, associated adjacent vertebral body abnormal bone marrow signal intensity consistent with that of osteomyelitis was noted (Fig 2). The average aneurysm diameter was 7.5 cm (range, 5–10 cm) and the average length was 8.0 cm (range, 6–10 cm). In one aneurysm, the celiac, superior mesenteric, and renal arteries were involved. Adjacent soft-tissue mass, stranding, and/or fluid were not appreciated in two aneurysms on T1-weighted images.

Nuclear Medicine
Increased radiotracer uptake was present in six (86%) of the seven patients examined with nuclear medicine. Aneurysms were located in the ascending aorta (n = 1, 14%), thoracoabdominal aorta (n = 2, 29%), juxtarenal aorta (n = 1, 14%), and infrarenal aorta (n = 3, 43%). The area of increased radiotracer uptake corresponded to the area of concern on the CT scan (Figs 1, 4).

Summary of Imaging Findings
Figure 6 illustrates the distribution of infected aortic aneurysms and compares with the distribution of arteriosclerotic aortic aneurysms reported in the literature (7,8). Aneurysm shape was saccular in 29 (94%) of 31 aneurysms and fusiform in two (6%). Vertebral body changes at CT, MR imaging, or radiography were noted in association with two (6%) of 31 aneurysms. Perianeurysmal gas was depicted on CT studies in two (7%) of 27 aneurysms, and periaortic soft-tissue mass, stranding, and/or fluid was seen on CT studies in 13 (48%) aneurysms. The average aneurysm diameter was 5.4 cm (range, 1–11 cm). The correlation of microbiologic results and imaging findings is shown in the Table.



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Figure 6. Comparison of location of infectious and arteriosclerotic aneurysms. The illustration on the left shows the location of the infected aneurysms, whereas the illustration on the right shows the location of arteriosclerotic aneurysms, as described in the literature. While almost 90% of arteriosclerotic aneurysms are located in the infrarenal aorta (IR), only one-third (n = 10) of infected aneurysms are found in this location. Infected aneurysms are found in locations where it would be unusual to find an arteriosclerotic aneurysm. AA = ascending aorta, DT = descending thoracic aorta, JR = juxtarenal aorta, PV = paravisceral aorta, R = renal artery, TA = thoracoabdominal aorta.

 

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Correlation of Infected Aortic Aneurysms with Imaging Findings

 

    DISCUSSION
 TOP
 ABSTRACT
 INTRODUCTION
 MATERIALS AND METHODS
 RESULTS
 DISCUSSION
 REFERENCES
 
Infected aortic aneurysms are also known as mycotic aneurysms; however, neither term seems to reflect the pathogenic process accurately. Sir William Osler used the term mycotic to describe the appearance of fresh fungal vegetation on the intimal surface of an aortic aneurysm in a patient with bacterial endocarditis (1). Since then, mycotic has been applied to infected aneurysms of all types, despite the fact that fungi are responsible for only a minority of aneurysms. In fact, none of the aneurysms in our study were caused by fungi. Although infected aortic aneurysm is a more inclusive term, the aorta is not always aneurysmal by conventional criteria (more than 50% luminal diameter dilatation). Acknowledging the imperfections of both terms, we chose to use infected aortic aneurysm to include any aortic dilatation of an infectious origin, regardless of its size and pathogen.

The pathophysiology of infected aortic aneurysm has been reported previously by several authors (9,10). Aortic infection develops when a pathogen offends a vulnerable vessel wall. The focus of infection can develop in a normal caliber vessel or an existing aneurysm. The infectious agent can either travel through the blood stream and harbor in the vasa vasorum of the arterial wall or implant on damaged intima, ulcerated arteriosclerotic plaques, or mural thrombus. Alternatively, the infectious agent can reach the artery either by contiguous spread of adjacent infectious process or by traumatic and/or iatrogenic inoculation. An infected aneurysm can occur anywhere in the vascular system.

Symptoms are nonspecific, laboratory data may be inconclusive, and a diagnosis of infected aortic aneurysm is often not suspected during clinical evaluation. Leukocytosis and an elevated erythrocyte sedimentation rate can be helpful in indicating this diagnosis but are not always present. Blood cultures can be negative for infection in as many as 47% of patients (5). Treatment consists of antibiotics and urgent surgery. The overall mortality rate is 16%–40% (3,11) but has been reported to be as high as 67% (12).

We present a series of imaging findings in 29 patients with infected aortic aneurysms. Imaging findings of infected aortic aneurysms are often suggestive of the diagnosis. Several characteristic features were commonly encountered in our series. Saccular shape, especially with a lobulated contour, was noted in all but two fusiform aneurysms. There was extensive mural thrombus in one of the fusiform aneurysms, and the surgical report described the infection confined to the mural thrombus.

The distribution of infected aortic aneurysms is different from the more commonly seen arteriosclerotic aneurysms. While the infrarenal aorta is by far the most common location (85%–87%) for arteriosclerotic aneurysms (7,8,13), in our series only 10 of 31 infected aneurysms were found in this location. The thoracic and abdominal aorta at or above the renal arteries was involved in almost 70% of infected aneurysms. A saccular aneurysm with lobulated contour was consistently seen with infected aneurysms on arteriography. Multiple aneurysms were uncommon and were seen in only two patients.

Cross-sectional imaging is valuable to demonstrate characteristic adjacent findings such as periaortic soft-tissue mass, stranding, and/or fluid. Helpful findings such as gas and vertebral body abnormalities were seen less commonly. Relatively rapid progression compared with the natural history of arteriosclerotic aneurysm was a feature that was present when sequential examinations were obtained. In the early stage, subtle periaortic inflammatory changes were detected; however, if these are not searched for, they may be overlooked. Nuclear medicine studies helped confirm the diagnosis in correlation with the cross-sectional findings; however, a study that does not reveal increased radiotracer uptake does not necessarily exclude this diagnosis. Previous reports of imaging findings in infected aortic aneurysm are mostly concordant with our findings. The CT appearance of infected aneurysms has been previously described (4,1423).

In our report, we chose to use the descriptor terms periaortic soft-tissue mass, stranding, and/or fluid. The following terms have been used to describe similar findings that are commonly associated with infected aneurysms: periaortic inflammation and/or soft tissue (4,17), retroperitoneal mass (15,16,24), encasing or contiguous mass (19), and paraaortic mass (23). Other findings that have been described previously in association with infected aneurysms are presence of gas (4,14,15,21) and rapid expansion or development (1416,20).

The association with vertebral body abnormalities has been recognized (4,14,18,19,22), including a review of the literature by McHenry et al that reported 70 cases of osteomyelitis and aortic infection (20). Lack of calcium in the involved aorta has been described as suggestive of an infected aneurysm (4,15,22); however, in our experience calcium was frequently found in association with infected aneurysms and was not a helpful differentiating feature from aneurysms of arteriosclerotic origin, which also have a high likelihood of calcification. The importance of this finding in the pathogenesis is unknown to us, since we did not have pathologic correlation. Renal infarct has been reported in a patient with an infected aneurysm; however, as previously hypothesized by Gonda et al (23), it appears that the adjacent location rather than the infected origin would be the cause. 111In white blood cell studies have been described as helpful in the diagnosis of infected aneurysms (16,25). Nuclear medicine examinations performed with white blood cell tagging (111In or HMPAO) or 67Ga are physiologic procedures that reproduce the migration of defense cells to the disturbed site. It cannot precisely aid in localization of the site of increased radiotracer uptake, but correlation with CT findings allows organ localization and facilitates the diagnosis of infected aneurysms.

Few reports have described MR findings in infected aortic aneurysms (16,26). MR angiography can demonstrate luminal caliber changes; however, T1-weighted sequences are necessary to demonstrate surrounding abnormalities that are typical of infected aneurysms. Ultrasonographic findings of infected aortic aneurysms have been previously described (27); however, disadvantages inherent to the technical limitations and aspects of this modality—such as patient body habitus, overlying bowel gas, and operator-dependent examination quality—limit the utility of this modality in the diagnosis of infected aortic aneurysms.

Awareness and recognition of imaging findings associated with infected aneurysms are critical for early diagnosis and institution of adequate therapy. Arteriography was formerly used (11,12) but has been largely replaced. At the Mayo Clinic, CT is the preferred imaging modality because it is widely available, fast, and able to depict associated findings, such as gas and periaortic findings. Furthermore, it is typically the first imaging examination that patients with vague general and abdominal complaints undergo. Newer techniques, such as multi–detector row helical CT and rapid three-dimensional reformatting, have further improved evaluation of the vascular system. CT has the advantage of showing both vessel anatomy and surrounding findings that are crucial in the diagnosis of infected aneurysms. Other cross-sectional imaging procedures, such as MR imaging, have similar diagnostic potential.

There are limitations to our study. First, the reviewer knew the diagnosis before the images were evaluated, which directed attention to the specific involved system and findings. Second, this was a retrospective study of patients from a single-institution referral center. Third, infected aortic aneurysm is an uncommon diagnosis, with a small number of cases. The statistical significance of the findings cannot be predicted with such small numbers and lack of control cases to calculate sensitivities and specificities. Fourth, the pool of imaging studies was heterogeneous, with use of different imaging modalities spanning a considerable period of time, during which the technology was changing. In addition, different modalities were used in all patients.

In summary, saccular aneurysm (especially lobulated), rapid expansion or development, and adjacent soft-tissue mass, stranding, and/or fluid in an unusual location are imaging findings that are highly suspicious for infected aortic aneurysm. Gas and vertebral body changes are helpful features, although they occur infrequently.


    FOOTNOTES
 
Author contributions: Guarantor of integrity of entire study, T.A.M.; study concepts and design, T.A.M., A.W.S., G.S.O., J.M.P.; literature research, T.A.M., G.S.O.; clinical studies, A.W.S., C.M.J.; data acquisition, T.A.M., G.S.O., M.T., A.W.S.; data analysis/interpretation, T.A.M., A.W.S.; manuscript preparation, definition of intellectual content, and editing, T.A.M., A.W.S.; manuscript revision/review, A.W.S., J.M.P., T.A.M.; manuscript final version approval, T.A.M., A.W.S.


    REFERENCES
 TOP
 ABSTRACT
 INTRODUCTION
 MATERIALS AND METHODS
 RESULTS
 DISCUSSION
 REFERENCES
 

  1. Osler W. The Gulstonian lectures on malignant endocarditis. BMJ 1885; 1:467-470.
  2. Parkhurst GF, Decker JP. Bacterial aortitis and mycotic aneurysm of the aorta. Am J Pathol 1955; 31:821-835.
  3. Oderich GS, Panneton JM, Bower TC, et al. Infected aortic aneurysms: aggressive presentation, complicated early outcome, but durable results. J Vasc Surg 2001; 34:900-908.[CrossRef][Medline]
  4. Sessa C, Farah I, Voirin L, et al. Infected aneurysms of the infrarenal abdominal aorta: diagnostic criteria and therapeutic strategy. Ann Vasc Surg 1997; 11:453-463.[CrossRef][Medline]
  5. Bennett DE. Primary mycotic aneurysms of the aorta: report of case and review of the literature. Arch Surg 1967; 94:758-765.[Medline]
  6. Mundth ED, Darling RC, Alvarado RH, et al. Surgical management of mycotic aneurysms and the complications of infection in vascular reconstructive surgery. Am J Surg 1969; 117:460-470.[CrossRef][Medline]
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