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Case ReportCase Report
Open Access

De Novo intracerebral aneurysm in a child with acquired immunodeficiency syndrome

Mohamad G. Bakhaidar, Naushad A. Ahamed, Mohammed A. Almekhlafi and Saleh S. Baeesa
Neurosciences Journal July 2015, 20 (3) 285-291; DOI: https://doi.org/10.17712/nsj.2015.3.20150064
Mohamad G. Bakhaidar
From the Division of Neurosurgery (Bakhaider, Baeesa), Department of Surgery, Department of Radiology (Ahamed) and Division of Neurology (Almekhlafi), Department of Medicine, Faculty of Medicine, King Abdulaziz University, Jeddah, Kingdom of Saudi Arabia
MBBS
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Naushad A. Ahamed
From the Division of Neurosurgery (Bakhaider, Baeesa), Department of Surgery, Department of Radiology (Ahamed) and Division of Neurology (Almekhlafi), Department of Medicine, Faculty of Medicine, King Abdulaziz University, Jeddah, Kingdom of Saudi Arabia
MBBS, DMRD
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Mohammed A. Almekhlafi
From the Division of Neurosurgery (Bakhaider, Baeesa), Department of Surgery, Department of Radiology (Ahamed) and Division of Neurology (Almekhlafi), Department of Medicine, Faculty of Medicine, King Abdulaziz University, Jeddah, Kingdom of Saudi Arabia
MSc, FRCPC
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Saleh S. Baeesa
From the Division of Neurosurgery (Bakhaider, Baeesa), Department of Surgery, Department of Radiology (Ahamed) and Division of Neurology (Almekhlafi), Department of Medicine, Faculty of Medicine, King Abdulaziz University, Jeddah, Kingdom of Saudi Arabia
MD, FRCSC
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    Figure 1

    Initial presentation study A) post-contrast T1-wighted MRI and B) at the level of the Circle of Willis and maximum-intensity projection reconstruction MRI image C) demonstrating normal flow void and vascular anatomy at the circle of Willis, particularly at the left ICA and MCA. MCA - middle cerebral arteries, ICA - internal carotid artery

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    Figure 2

    Second presentation MRI study: selected axial A) and coronal B) T2-weighted MRI at the region of circle of Willis showing an aneurysm at the junction between the distal ICA, M1-segment of MCA and the A1-segment of ACA, demonstrated as a flow void. This was well demonstrated with a C) 3D-reconstruction of the MRA. ICA - internal carotid artery, MCA -middle cerebral arteries, ACA - anterior and middle cerebral arteries

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    Figure 3

    Third presentation CT study selected axial non-contrast enhanced CT of the brain A) showing interval increase in the dimensions of the aneurysm and SAH due rupture of the aneurysm. There was hydrocephalus seen as marked dilatation of the temporal horns of the temporal horns of the lateral ventricles. 3D-reconstruction of a contrast-enhanced CTA B) after insertion of EVD, demonstrating the large fusiform aneurysm at the junction between the distal ICA, M1-segment of MCA and the A1- segment of ACA. The bony landmarks of the cranial fossa and the anterior cloned process are also shown. MCA - middle cerebral arteries, ICA - internal carotid artery, EVD - external ventricular drain, ACA- anterior and middle cerebral arteries, CTA - CT angiography, SAH - subarachnoid hemorrhage

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    Figure 4

    Intraoperative microscopic photograph through A) left frontotemporal craniotomy and transsylvian approach demonstrating the extent of the aneurysm, B) Repair of the fusiform ICA/MCA aneurysm was reconstructed with 2 fenestrated aneurysm clips. MCA - middle cerebral arteries, ICA - internal carotid artery.

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    Figure 5

    Selected coronal non-contrast CT image of the brain A) showing the clip applied across the aneurysm. Maximum-intensity projection reconstruction B) and 3D reconstruction of the postoperative contrast-enhanced MRA, demonstrates the reconstruction of the aneurysm and the patent distal circulation.

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    Table 1

    Summary of all reported pediatric cases of HIV-related aneurysmal vasculopathy.

    Year /No. of casesAge at aneurysm diagnosis (years)/gender/HIV sourcePresentationRadiological modality/Radiological findings/vessels involvedManagementOutcome
    Kure et al, 1989146 yrs/male/congenitalAphasia and quadriplegiaFusiform dilatation of circle of WillisNSDeath after 25 days in the hospital
    Lang et al, 1991198 yrs/male/congenitalNSFusiform dilatations of left ICA, MCA, and ACAAZT 5 years before CNS eventDied after one month secondary to cardiomyopathy
    Husson et al, 199213
    111 yrs/male/blood transfusionAsymptomaticMultiple saccular aneurysms of right MCA and fusiform aneurysm of left ACA and MCADDI one year prior to the presentation changed to AZT after aneurysm diagnosisCNS symptoms after 16 months
    212 yrs/male/blood transfusionAsymptomaticmultiple aneurysmal dilatations of the right MCA and ACADDI was continued after the diagnosisRemained asymptomatic
    312 yrs/female/congenitalFever, lethargy, seizure and upper limbs weaknessMultiple fusiform ICA, ACA, MCA and right PCA aneurysmsNSDeath within 2 months of presentation
    Dubrovsky et al, 19982113 yrs/male/uncertainAcute right hemiparesisFusiform dilatations of left supraclinoid ICA and proximal ACA and MCAAZT 18 months prior to the presentation, continued after diagnosis of the aneurysmDeath after 3 months secondary to cerebral infarction
    211 yrs/female/congenitalAcute change in mental statusFusiform aneurysms of left ICA and proximal MCA and bilateral PCAAZT started one year prior to the presentationDeath after 6 months secondary to infection
    36 yrs/female/CongenitalSeizureMultiple fusiform aneurysms of the right ICA and proximal right MCAAZT since 2-year-old. Radiotherapy for brain lymphomaNeurological status worsened gradually. Died later secondary to HIV-enteropathy
    412 yrs/male/blood transfusionHeadache and left-sided weaknessFusiform aneurysms of left ICA, MCA, and ACAART (DDI 2 years before the presentationMultiple opportunistic infections after the presentation died after 36 months
    510 yrs/male/perinatalCollapsed at schoolNot carried outDDI started 2 years prior to the presentationDeath at presentation
    Fulmer et al, 1998511 yrs/female/congenitalAsymptomaticMultiple ICA, MCA, and ACA fusiform aneurysmsObservationDeath after 3 years was secondary to other AIDs complications
    Mazzoni et al, 2000158 yrs/female/congenitalSudden loss of consciousness followed by seizure and mild hemiparesismultiple saccular and fusiform aneurysms in the proximal arteries, predominantly, in the left MCAAZT was replaced with DDI at the age of 3 years. HAART (AZT, 3TC, RTV) was initiated after aneurysm diagnosisPatient recovered after one month. After 4 months, repeated MRA showed no changes in the aneurysms
    Carvalho neto et al, 200166 yrs/male/congenitalSeizureAneurysmal dilatation of circle of Willis, more in the right.AZT and DDI were started at the age of 2 years. Supportive management for the CNS eventThe seizures stopped, and the patient was discharged with follow up in the clinic
    Nunes et al, 200132 months old/female/congenitally-acquiredRight hemiparesis and comaSaccular aneurysm of left basilar artery.IV AZT at birth. She was on AZT and DDI at presentation. Conservative management for SAHDeath after 12 days of SAH
    Patsalides et al, 2002207 cases, (7yrs – 15 yrs), 5 males and 2 females, 4 perinatal and 3 through blood transfusionNSAneurysms involved ICA, MCA, ACA, PCA, basilar and vertebral arteriesAll were taking ART before the diagnosis of aneurysmal arteriopathy2 cases were alive through out the observation period; 4 cases died secondary to other AIDS-related complications and a single case died secondary to CNS complications
    Petropolous et al, 20031712 yrs/male/NSAsymptomaticMultiple saccular aneurysms of proximal right ICA and proximal basilar arteryContinued the earlier started HAART (AZT, 3TC, NVP) with follow-up of the aneurysmsAfter 2 years follow-up, no new CNS symptoms, and MRI showed no changes
    Martinez-Longoria et al, 2004112 yrs/female/congenitalHeadache, transient left hemiparesis, blurred visionLeft ICA obstruction, stenosis in infraclinoid right ICA and fusiform dilatations of the right ICA bifurcation extends to right MCA and ACAInitially on AZT. SQV and 3TC were started 3 month before CNS event. HAART regime (Kaletra® (LPV/RTV), 3TC and D4T) and aspirin was started after the CNS eventMRI after 15 months showed complete resolution of the aneurysm. No neurological event was occurred over 2 years follow-up
    Mahadevan et al, 20071616 yrs/male/not knownHeadache, vomiting, slurred speech and weaknessFusiform dilatations of bilateral vertebral, basilar artery, right ICA, and MCAA twist drill and ventricular tap did reduce the intracranial pressureDeath within hours of presentation
    Thakker and Bhatia 20091012 yrs/male/congenitalHeadache and right hemiparesisFusiform aneurysms of the left supraclinoid ICAART 4 months prior to the presentation. Conservative management of the aneurysmNo reported the death or other CNS manifestations
    Demopolous et al, 200918
    112 yrs/male/NSRight hemiparesisFusiform right ICA aneurysmART for 5 years prior to the presentationComplete neurological recovery
    26 yrs/female/NSLeft hemiparesisFusiform dilatations of right ICA, right vertebral, and basilar arteryART for 6 months prior to the presentationThe residual weakness with neurocognitive impairment
    37 yrs/Male/NSRight hemiparesisMultiple aneurysms of vessels of the circle of WillisDid not receive ARTDeath
    Savitr sastri et al, 2011813 yrs/Male/NSAphasia and right hemiplegiaFusiform dilatations of bilateral supraclinoid ICAsExternal ventricular drain insertedDeath within hours of presentation
    Schieffelin et al, 20134
    17 HIV-infected pediatric cases were reported to have cerebral aneurysm with no specific demographicCNS symptomsAneurysmal dilatation of arteries in the circle of WillisDDI at the time of CNS eventAlive
    2blurred visionMultiple aneurysms, multiple infarctsHAART at the time of CNS eventDied
    3seizures, right hemiparesisInternal carotid artery aneurysmHAART at the time of CNS eventDied
    4CNS symptomsAneurysm of left ACA and narrowing of right MCAHAART at the time of CNS eventAlive
    5HemiplegiaFusiform CNS aneurysmHAART at the time of CNS eventAlive
    6CNS symptomsMultiple CNS aneurysmsHAART at the time of CNS eventAlive
    7CNS symptomsDiffuse CNS aneurysms with ectasiaD4T, NVP at the time of CNS eventDied
    Current Case7 yrs/Male/CongenitalHeadache and altered level of consciousnessfusiform aneurysm at left ICA bifurcation, and proximal ACA and MCAClipping of the aneurysm. Started on HAART before dischargeDischarged in a stable neurological condition to be followed up in the clinic
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    De Novo intracerebral aneurysm in a child with acquired immunodeficiency syndrome
    Mohamad G. Bakhaidar, Naushad A. Ahamed, Mohammed A. Almekhlafi, Saleh S. Baeesa
    Neurosciences Journal Jul 2015, 20 (3) 285-291; DOI: 10.17712/nsj.2015.3.20150064

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    De Novo intracerebral aneurysm in a child with acquired immunodeficiency syndrome
    Mohamad G. Bakhaidar, Naushad A. Ahamed, Mohammed A. Almekhlafi, Saleh S. Baeesa
    Neurosciences Journal Jul 2015, 20 (3) 285-291; DOI: 10.17712/nsj.2015.3.20150064
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