Abstract
A diagnostic challenge arises when a patient presents with a ring-enhancing lesion of the brain in the setting of both metastatic cancer and a source of infection. We report a case depicting this dilemma in an 80-year-old man with a history of metastatic oral squamous cell carcinoma who presented for left-sided hemiparesis. Computed tomography and magnetic resonance imaging revealed a ring-enhancing lesion of the right parietal vertex without signs of stroke. He was also found to have an aneurysm of the right common carotid artery with abnormal surrounding soft tissue density and gas, findings suspicious for a mycotic aneurysm. The likelihood of the brain lesion being an abscess formed by septic embolization was raised, leading to the recommendation to surgically explore the brain lesion and repair the aneurysm. Nevertheless, a high index of suspicion for a brain abscess and mycotic aneurysm is necessary in this type of clinical scenario.
Keywords: Ring-enhancing brain lesion, Mycotic aneurysm, Abscess
Introduction
Brain metastasis from head and neck squamous cell carcinoma (SCC) occurs in less than 1% of all reported cases [1]. Metastasis of oral SCC to remote regions of the brain is an even rarer occurrence with only a few cases reported in literature [2], [3]–4]. The incidence of mycotic aneurysms is also low, as 0.7%-3.0% of aortic aneurysms are infectious in origin [5]. There are even fewer reported cases of extracranial mycotic aneurysm associated with brain septic embolization [6], [7]–8]. We report a case of a man with a history of metastatic oral SCC who presented for weakness and was found to have a ring-enhancing brain lesion and simultaneous aneurysm of the right common carotid artery suspicious for a mycotic pseudoaneurysm. Because of concern for infection, the patient underwent surgical exploration of the brain lesion, revealing a pyogenic abscess, most likely from septic embolization from the mycotic aneurysm. This case is worthwhile to share for 2 major reasons. Firstly, it is extremely uncommon for a brain abscess to develop from septic embolization of an extracranial mycotic aneurysm. Secondly, the patient's history of metastatic SCC added an extra diagnostic challenge for the radiologist, as the brain lesion masqueraded as metastasis. Diagnosing brain metastasis would have led to drastically different management decisions.
Case report
An 80-year-old man with a history of oral SCC presented to the emergency department for left upper and lower extremity weakness for the last 3 days. He had no associated sensory symptoms or any symptoms in the face. On review of systems, he denied speech or vision changes, dizziness, headache, seizure, fever, urinary symptoms, chest pain, cough, or shortness of breath. He denied any recent falls or head trauma. About 2 weeks prior, he presented for hemoptysis due to bleeding of his tongue cancer mass, so he underwent endovascular embolization of multiple branches of the bilateral, external carotid arteries.
His past medical history is relevant for poorly-differentiated SCC of the base of the tongue (TNM stage: cT2N2b) which had spread to lymph nodes and was deemed terminal. He had tracheostomy and gastrostomy tubes placed about 2 months prior. He had not recently traveled anywhere. He was only taking acetaminophen as needed.
The patient's vital signs remained within normal limits. His physical exam was significant for ⅘ strength in the left upper and lower extremities with an NIH stroke scale of 2. Laboratory tests were unremarkable. No blood cultures were taken.
Computed tomography (CT) of the brain without contrast enhancement (Fig. 1) revealed a region of hypodensity at the right parietal vertex with a focal circular lesion measuring 15 mm in the anteroposterior dimension with surrounding adjacent edema. It also showed a smaller focus adjacent to the large lesion. There was no acute infarct or hemorrhage.
Fig. 1.
Axial (A) and sagittal (B) non-enhanced CT showing a region of hypodensity at the right parietal vertex with a focal circular lesion (arrows) measuring 15 mm in the anteroposterior dimension with surrounding adjacent edema.
CT angiography of the head and neck with intravenous (IV) contrast (Fig. 2) revealed interval development of a large, eccentric, saccular aneurysm from the distal right common carotid artery. It also showed asymmetry of the soft tissues lateral to the right hyoid bone with displacement of the styloid process and dislocation of stylohyoid articulation. Abnormal soft tissue density and gas surrounded this region. The aneurysm and soft tissue abnormalities enlarged since they were first discovered 2 weeks prior, after the patient's arterial embolization procedure.
Fig. 2.
Axial (A-B) and coronal (C) CT angiography showing a large, eccentric, saccular aneurysm (arrows) in the distal right common carotid artery. They also show asymmetry of the soft tissues lateral to the right hyoid bone with displacement of the styloid process and dislocation of stylohyoid articulation. Abnormal soft tissue density and gas (arrowhead) surrounds this region. (A) was taken 2 weeks prior to admission and a day after embolization procedure. (B & C) were taken on admission.
Magnetic resonance imaging (MRI) was obtained for further evaluation. MRI of the brain with and without IV gadolinium contrast (Fig. 3) revealed a 2 cm lesion at the right parietal vertex with peripheral ring enhancement and avid restricted diffusion. It also showed a medially-adjacent 1 cm lesion and an anteriorly-adjacent sub-1 cm lesion. There was significant surrounding vasogenic edema. MRI of the neck with IV contrast showed an irregular aneurysm at the right carotid bulb and diffuse soft tissue enhancement that was better characterized on CT.
Fig. 3.
MRI of the brain without (A) and with (B-D) gadolinium enhancement. (A) shows a 2 cm lesion (arrow) at the right parietal vertex. (B) shows the same 2 cm lesion (arrow) with peripheral ring enhancement and avid restricted diffusion of central fluid. (C) shows a medially adjacent 1 cm lesion (arrowhead). (D) shows an anteriorly adjacent sub-1 cm lesion (arrowhead).
Because of concern for infection, the patient was initially started on broad-spectrum antibiotics with vancomycin, cefepime, and metronidazole. He subsequently underwent surgical exploration of the brain lesion. An abscess was found and aspirated. Cultures of the brain abscess grew Streptococcus anginosus, and his antibiotic regimen was switched to ceftriaxone and metronidazole based on susceptibility results. His neurological status is currently improving. Surgical repair of the carotid aneurysm to prevent rupture is currently planned.
Discussion
The differential diagnosis for a ring-enhancing cerebral lesion commonly includes metastasis, abscess, glioblastoma, infarct, contusion, demyelinating disease, radiation necrosis, or resolving hematoma [9]. Radiographic features which favor an abscess include restricted diffusion of central fluid content, thin and regular enhancing wall, intermediate to low T2 signal capsule, and extensive surrounding edema relative to lesion size [10].
A mycotic aneurysm is a dilation of an arterial wall due to infection. Risk factors for the development of a mycotic aneurysm include arterial injury, antecedent infection, impaired immunity (eg, cancer), atherosclerosis, and pre-existing aneurysm [11], [12], [13], [14], [15]–16]. There are 4 major etiologies for a mycotic aneurysm: direct bacterial inoculation, bacteremic seeding, contiguous infection, and septic emboli from infective endocarditis [17], [18]–19]. Direct bacterial inoculation can result from arterial injury during a catheter-involving procedure. Injury to an arterial wall could also lead to the formation of a pseudoaneurysm, which is defined as a collection of blood that has leaked out of an artery but is then confined by the surrounding tissue. The most useful imaging study for diagnosing a mycotic aneurysm is CT angiography [20]. Findings suggestive of a mycotic aneurysm on CT angiography include saccular, eccentric, or multilobulated appearance, surrounding soft tissue inflammation, and intramural or surrounding air [20], [21], [22]–23].
Making the diagnosis required a contextualization of imaging on clinical history. The patient's aneurysm was likely a mycotic pseudoaneurysm based on its radiographic features and interval development. The most likely etiology was direct bacterial inoculation from vascular injury during the patient's embolization procedure. The aneurysm and surrounding tissue abnormalities rapidly developed soon after. Less likely was that catheter-related injury led to a non-infectious pseudoaneurysm, and the soft tissue abnormalities could be a sequela of embolization and post-radiation necrotic changes.
Despite the patient's history of metastatic oral SCC, the radiographic features of his large, ring-enhancing brain lesion favored an abscess. Particularly, the lesion demonstrated restricted diffusion of central fluid and extensive surrounding edema. In terms of etiology, the recent catheter-directed embolization procedure could have led to bacteremia. Moreover, the diagnosis of a mycotic pseudoaneurysm further raised the likelihood of a brain abscess from possible septic embolization.
Diagnosis based on imaging heavily affected management decisions for this patient. Concern for infection led to the decision to start broad-spectrum antibiotics. Raising the likelihood of a brain abscess led to the recommendation to surgically explore the lesion. Had the diagnostic pendulum not swung away from metastatic disease, the patient may have been recommended surveillance of the lesion over time with palliative care rather than immediate intervention.
This case report demonstrates the important role of a diagnostic radiologist in piecing together multiple imaging findings and clinical history to solve a patient's case and affect management decisions. A brain abscess should be considered when a patient with a history of metastatic cancer presents with a cerebral ring-enhancing lesion and an aneurysm suspicious for infection.
Patient consent
Written, informed consent was obtained for publication of this case report was obtained from the patient.
Footnotes
Competing Interests: All authors of this case report have no interests to declare.
References
- 1.Barrett TF, Gill CM, Miles BA, Lloreta AMC, Bakst RL, Fowkes M. Brain metastasis from squamous cell carcinoma of the head and neck: a review of the literature in the genomic era. Neurosurg Focus. 2018;44(6) doi: 10.3171/2018.2.focus17761. [DOI] [PubMed] [Google Scholar]
- 2.Leimert M, Juratli TA, Lindner C, Geiger KD, Gerber J, Schackert G. An extremely rare, remote intracerebral metastasis of oral cavity cancer: a case report. Case Rep Med. 2013;2013:1–4. doi: 10.1155/2013/257046. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 3.Hardee P, Hutchison I. Intracranial metastases from oral squamous cell carcinoma. Br J Oral Maxillofac Surg. 2001;39(4):282–285. doi: 10.1054/bjom.2001.0648. [DOI] [PubMed] [Google Scholar]
- 4.Ruzevick J, Olivi A, Westra WH. Metastatic squamous cell carcinoma to the brain: an unrecognized pattern of distant spread in patients with HPV-related head and neck cancer. J Neurooncol. 2013;112(3):449–454. doi: 10.1007/s11060-013-1075-9. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 5.Majeed H and Ahmad F. Mycotic aneurysm. Updated 2021 Jan 20. StatPearls. Treasure Island (FL): StatPearls Publishing; 2021. Available from: https://www.ncbi.nlm.nih.gov/books/NBK560736/ The access date was May 5, 2021.
- 6.Papadoulas S, Zampakis P, Liamis A, Dimopoulos PA, Tsolakis IA. Mycotic aneurysm of the internal carotid artery presenting with multiple cerebral septic emboli. Vascular. 2007;15(4):215–220. doi: 10.2310/6670.2007.00043. [DOI] [PubMed] [Google Scholar]
- 7.Imamura J, Watanabe Y. Multiple brain abscesses associated with a mycotic aneurysm of the left common carotid artery. J Neurosurg. 1986;64(2):325–327. doi: 10.3171/jns.1986.64.2.0325. [DOI] [PubMed] [Google Scholar]
- 8.Pocar M, Moneta A, Pelenghi S, Donatelli F, Tresoldi F, Scomazzoni F. Mycotic aortic aneurysm presenting as multiple cerebral abscesses. Acta Neurochirurgica. 1998;140(3):289–290. doi: 10.1007/s007010050098. [DOI] [PubMed] [Google Scholar]
- 9.Nadgir R, Yousem DM. Elsevier; 2017. Neuroradiology: the requisites. [Google Scholar]
- 10.Falcone S, Post MJ. Encephalitis, cerebritis, and brain abscess: pathophysiology and imaging findings. Neuroimaging Clin N Am. 2000;10(2):333–353. PMID: 10775955. [PubMed] [Google Scholar]
- 11.Qureshi T, Hawrych AB, Hopkins NF. Mycotic aneurysm after percutaneous transluminal femoral artery angioplasty. J R Soc Med. 1999;92(5):255–256. doi: 10.1177/014107689909200515. PMID: 10472268; PMCID: PMC1297183. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 12.Samore MH, Wessolossky MA, Lewis SM, Shubrooks SJ, Jr, Karchmer AW. Frequency, risk factors, and outcome for bacteremia after percutaneous transluminal coronary angioplasty. Am J Cardiol. 1997;79(7):873–877. doi: 10.1016/s0002-9149(97)00006-4. PMID: 9104897. [DOI] [PubMed] [Google Scholar]
- 13.Brown SL, Busuttil RW, Baker JD, Machleder HI, Moore WS, Barker WF. Bacteriologic and surgical determinants of survival in patients with mycotic aneurysms. J Vasc Surg. 1984;1(4):541–547. PMID: 6436514. [PubMed] [Google Scholar]
- 14.Johansen K, Devin J. Mycotic aortic aneurysms. A reappraisal. Arch Surg. 1983;118(5):583–588. doi: 10.1001/archsurg.1983.01390050059011. PMID: 6687677. [DOI] [PubMed] [Google Scholar]
- 15.Oderich GS, Panneton JM, Bower TC, Cherry KJ, Jr, Rowland CM, Noel AA. Infected aortic aneurysms: aggressive presentation, complicated early outcome, but durable results. J Vasc Surg. 2001;34(5):900–908. doi: 10.1067/mva.2001.118084. PMID: 11700493. [DOI] [PubMed] [Google Scholar]
- 16.Macbeth GA, Rubin JR, McIntyre KE, Jr, Goldstone J, Malone JM. The relevance of arterial wall microbiology to the treatment of prosthetic graft infections: graft infection vs. arterial infection. J Vasc Surg. 1984;1(6):750–756. doi: 10.1067/mva.1984.avs0010750. PMID: 6436515. [DOI] [PubMed] [Google Scholar]
- 17.Baddour LM, Wilson WR, Bayer AS, Fowler VG Jr, Tleyjeh IM, Rybak MJ, et al. American Heart Association Committee on Rheumatic Fever, Endocarditis, and Kawasaki Disease of the Council on Cardiovascular Disease in the Young, Council on Clinical Cardiology, Council on Cardiovascular Surgery and Anesthesia, and Stroke Council. Infective endocarditis in adults: diagnosis, antimicrobial therapy, and management of complications: a scientific statement for healthcare professionals from the American Heart Association. Circulation. 2015;132(15):1435-86. doi: 10.1161/CIR.0000000000000296. Epub 2015 Sep 15. Erratum in: Circulation. 2015 Oct 27;132(17):e215. Erratum in: Circulation. 2016 Aug 23;134(8):e113. Erratum in: Circulation. 2018 Jul 31;138(5):e78-e79. PMID: 26373316. [DOI] [PubMed]
- 18.Ernst CB, Campbell HC, Jr, Daugherty ME, Sachatello CR, Griffen WO., Jr. Incidence and significance of intra-operative bacterial cultures during abdominal aortic aneurysmectomy. Ann Surg. 1977;185(6):626–633. doi: 10.1097/00000658-197706000-00003. PMID: 324416; PMCID: PMC1396230. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 19.Garb M. Appendicitis: an unusual cause of infected abdominal aortic aneurysm. Australas Radiol. 1994;38(1):68–69. doi: 10.1111/j.1440-1673.1994.tb00132.x. PMID: 8147809. [DOI] [PubMed] [Google Scholar]
- 20.Vogelzang RL, Sohaey R. Infected aortic aneurysms: CT appearance. J Comput Assist Tomogr. 1988;12(1):109–112. doi: 10.1097/00004728-198801000-00021. PMID: 3335648. [DOI] [PubMed] [Google Scholar]
- 21.Ou P, Sidi D, Bonnet D, Brunelle F. Infected pulmonary artery aneurysms: CT imaging findings. Eur J Cardiothorac Surg. 2006;29(2):248. doi: 10.1016/j.ejcts.2005.11.011. Epub 2006 Jan 11. PMID: 16376097. [DOI] [PubMed] [Google Scholar]
- 22.Gomes MN, Choyke PL. Infected aortic aneurysms: CT diagnosis. J Cardiovasc Surg. 1992;33(6):684–689. PMID: 1287005. [PubMed] [Google Scholar]
- 23.Lee WK, Mossop PJ, Little AF, Fitt GJ, Vrazas JI, Hoang JK. Infected (mycotic) aneurysms: spectrum of imaging appearances and management. Radiographics. 2008;28(7):1853–1868. doi: 10.1148/rg.287085054. PMID: 19001644. [DOI] [PubMed] [Google Scholar]



