Case Reports in Neurological Medicine

Volume 2013 (2013), Article ID 812158, 6 pages

http://dx.doi.org/10.1155/2013/812158

Case Report

Cerebral Aneurysms: A Rare Feature of Behçet's Disease—A Case Report and Review of the Literature

Samia Younes,¹ Yosra Cherif,¹ Narjes Mokni,¹ Olfa Berriche,¹ Baha Zantour,¹ Amel Boughammoura,² Mahbouba Frih-Ayed,² Saida Jerbi,³ and Mohamed Habib Sfar¹

¹Department of Endocrinology and Internal Medicine, Tahar Sfar University Hospital of Mahdia, Hiboun District, 5100 Mahdia, Tunisia

²Department of Neurology, Fattouma Bourguiba University Hospital of Monastir, 1st June Street, 5000 Monastir, Tunisia

³Department of Medical Imagery, Tahar Sfar University Hospital of Mahdia, Hiboun District, 5100 Mahdia, Tunisia

Received 8 June 2013; Accepted 10 July 2013

Academic Editors: K. Arnautovíc, Ö. Ateş, and H. Ikeda

Copyright © 2013 Samia Younes 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.

Abstract.

Behçet's disease (BD) is a multisystem vascular inflammatory disease with several clinical manifestations. Intracranial aneurysms are an extremely rare but nevertheless severe complication of BD. We report a case of a 44-year-old man. The diagnosis of BD was made based on the presence of recurrent oral aphthous ulcers and positive human leukocyte antigen (HLA-) B51 in the absence of evidence of other diseases. MRI showed an ancient ischemic right capsulolenticular lesion, subacute white matter hypersignals of the left capsule lenticular region, and multiple arterial aneurysms. The patient underwent two-month systemic high-dose corticosteroids and immunosuppressive therapy associated with severe neurological deficiency upon admission and severe impairment upon discharge. A thorough review of the literature showed 20 case reports of intracranial aneurysms in BD.

1. Introduction

Behçet’s disease (BD) is a chronic, relapsing multisystem vascular inflammatory disorder. Vasculitis is its major pathological feature. It mostly affected young adult men [1, 2]. Neurological involvement is relatively uncommon and it may be the first symptom in only 3% of patients [2]. Ischemic events and aneurysms due to Behçet’s disease are scarce and may cause life-threatening complications [3–7]. Their pathogenesis remains unknown [2, 8–10]. On account of the risk of serious bleeding complication, it is important to make the diagnosis as soon as possible. We report a rare case of neuro-Behçet in a 44-year-old man with unusual multiple cerebral aneurysms and stroke.

2. Case Report

A 44-year-old right-handed male, with previously healthy status and no family history, was admitted with complaints of acute, generalized headache associated with left arm and leg weakness. He had been suffering from oral aphthous ulcers for 5 years but no genital ulcers. One year ago, he was diagnosed with a cerebral ischemic stroke reveled with left hemiparesis. He developed significant behavioral changes, insomnia, and visual hallucinations that occurred 2 weeks prior to the outbreak of right hemiparesis. The patient was afebrile. He had a blood pressure of 130/80 mmHg, a pulse of 84 beats/min and a respiratory rate of 18 breaths/min. Physical examination revealed also oral aphthous ulceration but no genital scars due to healed ulcers. A thorough neurological examination revealed a normal conscience, no neck stiffness, but dysarthria, quadripyramidal syndrome with tetraparesis, predominant left motor deficit, and bilateral Babinski sign. Examination of the sensibility showed decreased senses of touch, pain, and temperature in the left side of the body. Computed tomography imaging and cerebral MRI disclosed an ancient ischemic right capsulolenticular lesion, with recent ischemic lesions in left capsule-lenticular region (Figure 1). MRI with gadolinium revealed enhancing lesions compatible with intracranial multiple arterial aneurysms (Figure 2). Thoracoabdominal computed tomography angiography had showed no extracranial aneurysms. Laboratory analysis showed a white blood cells count at 9.000 cells/mL with 85% neutrophils, a hemoglobin value at 10.8 g/dL, and a platelet count at 570.000 cells/mL. The erythrocyte sedimentation rate was over 111 mm/hour and the C-reactive protein was at 30 mg/L. Creatinine, electrolyte levels, liver tests, and coagulation studies were within the normal range. All serologic markers of hepatitis B and C, HIV, and syphilis were negative and no microorganisms could be identified from his blood and urine cultures. Immunological analysis including anti-nuclear and anti-phospholipid antibodies, rheumatoid factor, and anti-neutrophilic cytoplasmic antibodies were also within the referential range. Multiple laboratory tests and radiological studies ruled out a hypercoagulability syndrome and a heart disease. A Pathergy test was repeated and found to be clearly negative. The diagnosis of BD was made based on the presence of recurrent oral aphthous ulcers and positive human leukocyte antigen (HLA) B51 in the absence of evidence of other diseases.

Figure 1: Cerebral MRI axial section diffusion sequence showed bilateral capsule lenticular ischemic lesions (ancient at the right and recent at the left).

(a)

(b)

Figure 2: Axial and coronal cerebral MRI T1 gadolinium demonstrated several aneurysms of cerebral arteries.

Since then, the patient was treated with Methylprednisolone pulses linked with a high-dose regimen of prednisone (1 mg/kg/day) during two months, daily Azathioprine, and physical rehabilitation was started. Coil embolization of aneurysms was not performed because the aneurysms were numerous and there was no bleeding.

Ten months after discharge, despite marked regression of mental impairment and no further ischemic events, he developed a pseudobulbar effect including uncontrollable episodes of crying, dysarthria associated with urinary incontinence. The control MRI remained unchanged with persistent diffuse and unruptured aneurysmal dilatation and ancient cerebral stroke (Figure 3).

Figure 3: Cerebral MRI showed persistent multiple aneurysms 6 months after treatment.

3. Discussion

BD is a multisystemic recurrent inflammatory disorder affecting the eyes, skin and mucosa, joints, vascular system, lungs, gastrointestinal tract, and nervous system [2, 11, 12].

Its clinical pattern and outcomes are various and serious. Venous system’s involvement is more common than arterial system’s one [2]. The neurological features of BD are mainly related to vasculitis of cerebral vessels. The association of BD with cerebral aneurysms is scarce [2] and its pathogenesis remains unknown.

Peripheral aneurysms are likely more frequent than intracranial even underestimated [2, 11]. Benamour et al. reported only one cerebral aneurysm in 316 cases with BD [1]. Most instances occur, like BD, in men at the age of 41.1 years old (Table 1).

Table 1

Author/Ref.
Sex/Age
Diagnostic delay of BD
Clinical manifestations
Location
Other localizations of aneurysms
Medical treatment
Intervention
Follow-up

Katoh et al. [10]
M/29
/
/
MCA
/
/
Clipping
/

Buge et al. [4]
M/43
8 years
Hemiplegia
ACA, MCA, IC
Retinal an
Corticosteroids
No
/

Kerr et al. [17]
M/12
/
/
MCA, ACom, PCom, AChorA
/
Corticosteroids
Clipping
/

Tsuji et al. [7]
F/62
23 years
Headache, CD, SAH
Bilateral MCA, IC, ACom
No
/
clipping
/

Khodja et al. [8]
M/43
9 years
Lower limb monoparesia
ACom
celiac trunk AN Angiodysplasia AVM
Corticosteroids

Colchicine
No
/

Dietl et al. [15]
/
/
/
Bilateral IC
/
Corticosteroids

Colchicine
Coil
/

Ildan et al. [21]
M/28
3 years
SAH
ACom
No
Corticosteroids,

Cyclophosph.
Clipping
/

El Abbadi et al. [16]
M/44
2 years
CS (MCA)
Bilateral MCA
No
/
Clipping
/

Nakasu et al. [6]
M/57
19 years
SAH, paresia, confusional state
Bilateral MCA
/
/
Clipping
Relapse AN MCA disappeared after steroid therapy

Rosenstingl et al. [19]
M/36
0
SAH
SCER AN
No
Corticosteroids,

Cyclophosph.

Colchicine
Coil, angioplasty
Disappeared

Koçak et al. [20]
M/37
6 years before
Headache, cerebral hematoma
MCA
No
No
Clipping
Disappeared

Chi and Deruytter [5]
F/43
8 years
Headache, seizures, SAH
SCER AN
No
Received previously corticosteroids Cyclophosph.
Craniectomy
Recovered

Died: unknown cause

Itoh et al. [22]
M/65
25 years
Headache, ataxia
Medulla oblongata
No
/
/
/

Kizilkilic et al. [18]
(i) M/38

(ii) M/55
(i) 5 months after

(ii) /
(i) SAH, headache

(ii) Headache, SAH
(i) SCER AN

(ii) PICA
(i) Dissection pseudo an, tapered VA

(i) Coil

(ii) Coil
(i) recovered

(ii) recovered

Kaku et al. [9]
F/19
1 month
Headache, seizures, SAH, paresis
Bilateral MCA
No
Corticosteroids
Surgery
Recovered

Aktaş et al. [3]
M/38
4 years
Headache, SAH
Trunk of basilar artery
No
No
No
Died

Bahar et al. [23]
M/36
4 years
SAH
IC
SMA AN
Corticosteroids (4 years before)
Coil
Recovered

Agrawal et al. [13]
F/36
6 years
SAH
IC
No
Corticosteroids
Endovascular TRT
Recovered

Senel et al. [14]
M/45
/
SAH
PCA
No
No
Spontaneously thrombosed
Recovered

Okutucu et al. [24]
M/34
0
Headache
MCA
Coronary artery AN
Corticosteroids

Cyclophosph.

INF
Coil
Recovered

Our case
M/44
0
Hemiplegia
Multiple and bilateral cerebral arteries
No
Corticosteroids

Azathioprine
No
Recovered

MCA: middle cerebral artery, ACA: anterior cerebral artery, PCA: posterior cerebral artery, AN: aneurysm, IC: internal carotid, CS: cerebral stroke, CD: consciousness disturbance, SAH: subarachnoid haemorrhage, ACom: anterior communicating artery, AVM: arteriovenous malformation, SCER AN: superior cerebellar artery aneurysm, AChorA: anterior choroidal artery, PCom: posterior communicating artery, PICA: posterior inferior cerebral artery, VA: vertebral artery, SMA: superior mesenteric artery.

Table 1 summarizes 22 cases of intracranial aneurysms in BD patients previously reported in the literature. The age of these cases was ranged between 12 and 65 years and the male: female ratio was 4.25. The main clinical feature was acute subarachnoid hemorrhage in 12 patients unlike our case of aneurysms first identified as unruptured and associated with an ischemic stroke. The association of cerebral stroke with intracranial aneurysms is rather uncommon detected previously in 4 patients (cases 2, 8, 12, and 14). Cerebral hematoma was detected in 1 patient (case 11). The diagnosis of BD was often established before intracranial aneurysms and the preceding term ranged from 1 month to 25 years (mean: 8 years). Intracranial aneurysms were the first manifestation in 2 cases. Currently, the MRI is considered the most sensitive, noninvasive, and safe screening imaging for the accurate assessment of intracranial aneurysms [2]. Most of them are located in the anterior cerebral circulation, similar to those in the aneurysm cases without BD, and arise from middle cerebral artery (Table 1) and were multiple in 7 cases (Table 1) like our patient. Five of the patients had internal carotid artery aneurysms; 3 had superior cerebellar artery aneurysm (Table 1). Five cases were diagnosed with associated extracranial aneurysms: one retinal aneurysm, another celiac trunk, another superior mesenteric, another with coronary aneurysm, and several pulmonary aneurysms (Table 1). Until it may often be associated with extracranial locations, we might search peripheral arterial involvement which estimated in 7% of patients and it mostly affects the abdominal aorta and the femoral and pulmonary arteries [11]. Furthermore, our review showed peripheral thrombosis in 4 patients with different locations (Table 1). Unlike other cases, our patient had no extracranial aneurysms. Vascular complications such as dissection were mentioned in 2 cases and rupture in 13 cases. One case was associated with arteriovenous malformation; both conditions carry a high risk of delayed bleeding.

Our review of the literature showed that the cerebral aneurysms were mostly treated in 11 cases with steroid therapy, Colchicine in 3 cases, Cyclophosphamide in 3 cases, Interferon in 1 case, and Azathioprine associated with steroid therapy in our case (Table 1).

Many attempts were made with clipping in 7 patients and coil embolization in 6 cases and surgical resection was carried out in 2 cases. Given that data is missing for 13 cases, there was satisfactory result in 11 cases after a long-term follow-up; only 2 patients died and relapse of aneurysm of middle cerebral artery occurred in 1 case and was treated successfully with steroid therapy (Table 1). Our patient was treated with a high regimen of corticosteroids. He did not receive antiplatelet drugs because of the risk of major bleeding. He also underwent neither coil embolization nor surgery.

Vasculitis is more and more raised as the typical pathogenesis in arterial involvement of BD [7, 11, 12], but its part in cerebral aneurysms has not yet been clarified [8–10]. The inflammatory disorder may probably increase the risk of bleeding [13, 14]. Nevertheless, the histopathological examination of 2 cases (1 and 5) with intracranial aneurysms showed no vasculitis [15, 16]. Thus, it suggests the incidental aneurysm in BD, but the aneurysms whether extracranial or intracranial are more common in BD than other vasculitides. This would not be just a coincidence.

The diagnosis of neuro-Behçet can be tricky to establish in the absence of other criteria. Thereafter, the diagnosis of BD in our case was carried on the basis of recurrent oral aphthous ulcers and intracranial aneurysms and was strengthened by the positive human leukocyte antigen (HLA) B51 in the absence of evidence of other diseases. Then, the association of other vasculitides or clinical features at that time may support the diagnosis of BD.

Currently, corticosteroid and immunosuppressive therapy are warranted and beneficial when given in the early stage of the disease to prevent vascular complications and relapses [17]. Because of the multiple aneurysms, their histopathological properties, and the high risk of rupture, surgical resection is performed in carefully selected cases [17]. Many attempts have been made to manage these serious lesions by clipping or coil embolization and may be completely successful. It is difficult to predict its course and response to treatment. Intracranial aneurysms such as in BD carry a poor prognosis despite early and prompt treatment. Intracranial aneurysms rupture and dissection are often the dreadful complication, albeit rare [3, 5, 6, 8, 17–19], associated with a high mortality and poor neurological outcomes [4, 12]. Interestingly, the aneurysm disappears after corticosteroid regimen in several cases [6, 9, 19, 20]. In fact, our patient had no recurrence of cerebral stroke, but aneurysms persist and developed neurological and behavioral impairment upon discharge.

4. Conclusion

Intracranial aneurysm is an extremely rare but nevertheless severe complication of BD. The same lines of treatment used to manage vasculitis in BD and at time endovascular embolization should also be used to treat intracranial aneurysms related to BD. The literature, however, is limited to case reports, and the incidence of these lesions is unknown. It is possible that more of these lesions will be detected with increased use of noninvasive vascular imaging. More work is required to better delineate the natural history of this condition and to come up with treatment guidelines.

Conflict of Interests

The authors report no conflict of interests.

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