Mycotic Aneurysm Treated with Aneurysm Trapping. Case Report

Abstract

The authors describe a rare case of mycotic aneurysm (MA) associated with subarachnoid hemorrhage treated with aneurysm trapping. The literature on management and the surgical techniques are controversial due to lack of randomize trials.

Keywords

mycotic aneurysm - subarachnoid hemorrhage - endocarditis

Introduction

Mycotic cerebral aneurysm is one of many lesions due to infective endocarditis (IE) but still rare and potentially fatal complication. Medical treatment is based on antibiotics and in specific cases surgical treatment is required (craniotomy or endovascular). The absence of randomized trials generates a lack of consensus regarding the management of unruptured aneurysms. We present a case report of a patient diagnosed and treated surgically with improvement on follow-up with the trapping technique of the aneurysm.

Case Report

A 32-year-old man presented with sudden headache, high-grade fever with chills, and right hemiparesis. Sought medical attention and on the examination of admission, he was febrile (38°C). The pulse rate was regular (76 beats/min) and blood pressure was 130/70 mm Hg. Cardiac auscultation revealed soft first heart sound, normal aortic component, and a grade 3/6 mitral murmur. On neurologic examination he presented alert and conscious, with a right paretic gait and muscular strength grade I right-sided hemiparesis. After the new diagnosis of a febrile syndrome plus pyramidal syndrome the initial investigation was performed.

Investigations

Hemogram revealed leucocytosis (11,000/mm³) with predominant neutrophilia (70%) and normal platelet count (190,000). Urine examination, renal function test, and liver function test were normal. Transthoracic echocardiogram revealed a mitral thickening with perforation leading to severe mitral regurgitation with two jets.

Blood cultures (four samples) were positive after for Abiotrophia defectiva after 96 hour by the matrix-assisted laser desorption/ionization (MALDI TOF) MS method.

Computed tomographic (CT) angiogram and angiography revealed an M2 aneurysm with subarachnoid hemorrhage (SAH) ([Figs. 1] and [2]).

Fig. 1 CT of the head with Fisher IV subarachnoid hemorrhage (SAH).

Fig. 2 MCA M2 segment aneurysm.

Treatment

The patient was treated with antifailure medications along with injectable antibiotics for IE for 8 weeks.

The patient was submitted to surgery (pterional craniotomy) with trapping of the aneurysm with success.

Outcome and Follow-up

The patient was treated with antibiotics and close monitoring for eventual neurologic symptoms worsening. The patient became afebrile and the symptoms leading to heart failure improved with the medical therapy after 10 days. After 8 weeks we performed a control magnetic resonance imaging (MRI) angiogram who revealed that the previous lesion increased ([Fig. 3]). After surgery the patient improved the previous deficit on 3 months follow-up (from grade I–IV hemiparesis) ([Fig. 4]).

Fig. 3 Angiogram revealing increase of the lesion.

Fig. 4 Post-op CT.

Discussion

The epidemiologic profile of IE has changed substantially over the last few years, especially in industrialized nations. Newer predisposing factors have emerged—valve prostheses, degenerative valve sclerosis, intravenous drug abuse—associated with increased use of invasive procedures at risk for bacteremia, resulting in health care–associated IE.[1]

In developed countries, the incidence of IE ranges from 3 to 9 cases per 100,000 per year, and it is twice as common in men.[1]

Staphylococcus aureus is the most common organism. Up to 30% of those having bacteremia with Staphylococcus will develop endocarditis and 75% of patients with IE have structural abnormalities on their hearts.[1] [2]

A. defectiva, a nutritionally variant Streptococcus (NVS), represents a rare but clinically important cause of IE initially described by Frenkel and Hirsch in 1961[3] as fastidious gram-positive bacterium and modified by Bouvet et al in 1989[4] who proposed the names Streptococcus defectivus and Streptococcus adjacens, following the use of DNA—DNA hybridization studies.[1] [5] [6]

A. defectiva endocarditis is a rare cause of endocarditis with rates around 5% of all cases of streptococcal endocarditis. There are around 100 cases of A. defectiva endocarditis in the literature. It predominantly occurs in the setting of preexisting heart disease (90%); prosthetic heart valves are involved in 10% of patients. There are no published cases on adults without previously documented valvular heart disease developing.[5] [6]

The 1-year rate of IE mortality is around 30%. Neurologic complications, most commonly cerebral embolism, are seen in 20 to 40% of the patients and are associated with high morbidity and mortality. The reported incidence of mycotic cerebral aneurysms is 2 to 3% of all the patients with IE. This is possibly underestimated, because most patients remain asymptomatic and the aneurysm may resolve after antibiotic therapy.[2] [7]

The symptoms usually include headache (83%), fever (67%), vomiting (50%), ocular palsy (25%), seizures (21%), behavioral changes (21%), hemiparesis (21%), drowsiness (17%), and loss of consciousness (17%).[1] [7]

The clinical diagnosis of IE is usually made based on modified Duke criteria and the neurologic complications with CT and magnetic resonance angiography.[1] [7]

Authors such as Thuny et al[8] reported that cerebral and thoracoabdominal CT revealed silent emboli in only 8% of patients. Cooper et al[9] performed MRI of the brain in 40 patients with IE and found acute brain embolization in 80% of patients.[10]

Several authors have recommended the antimicrobial therapy tailored by culture for 6 to 8 weeks along with close follow-up as the first line of treatment for unruptured intracranial aneurysms and serial imaging. Invasive procedures (microsurgery/endovascular) are indicated for very large, enlarging, or ruptured aneurysm.[1] [10]

Surgical management of mycotic aneurysm (MA) depends on several factors, including size, location, expertise of the surgeon (on microsurgery or endovascular) ([Table 1]), and if the aneurysm has ruptured. There are no data comparing microsurgery versus endovascular.[11] [12] Ruptured MAs are managed by either open or endovascular means, following which a 2- to 3-week delay is recommended prior to cardiac valve replacement. Microsurgery in this case is technically difficult, as MAs tend to be fusiform with poorly defined necks and friable walls. Proximal ligation is therefore often necessary. Anastomotic procedures that can spare distal vessels in eloquent areas are sometimes possible. Endovascular therapies are less invasive alternatives that may be more appropriate in patients who are unfit for surgery due to cardiac disease. Detachable coils are preferred for proximal aneurysms, whereas distal aneurysms that are not accessible to microcatheters can be managed with acrylic glue or autologous clot injections.[2] [11] [12]

Table 1 Presentation of reported patients treated with endovascular versus current patient (microsurgery)

Reference (year)	Age (y)	Clinical presentation	Etiology	Pathogen	Follow-up (mo)	Modified Rankin Scale score
Current patient, 2015	32	Fever, headache, and hemiplegia	Bacterial	Abiotrophia defectiva	3	0
Ding et al, 2014[13]	35	Diplopia	Bacterial endocarditis	Streptococcus mitis	3	0
Sugg et al, 2006[14]	47	Hemiplegia, headache	Bacterial endocarditis	Unknown	None	3
Yen et al, 2007[15]	46	Ophthalmoplegia	Meningitis	Streptococcus constellatus	6	1
Appelboom et al, 2007[16]	10	Ophthalmoplegia	Meningitis	Streptococcus pneumoniae	3	0

Conclusion

IE is a serious disorder very often in developing countries that is frequently complicated when associated with neurologic disease including ischemic and hemorrhagic stroke. The surgical management of the underlying disease still lacks of randomized trials and sets a new opportunity for new studies regarding the matter. A multidisciplinary collaborative approach is critical to optimizing outcomes.

Disclosures

The authors declared no potential conflicts of interest.

• References

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Publication History

Received: 17 July 2015

Accepted: 26 September 2015

Publication Date:
16 November 2015 (online)