arteriovenous malformations by dr. shikher shrestha, fcps, neurosurgery , ninas, nepal
TRANSCRIPT
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Arteriovenous Malformations
Shikher ShresthaNINAS
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Introduction
Distinct entity – fascinated and terrified neurosurgeons for decades
Vascular lesion – risk of debilitating hemorrhage
Do not develop de novo but remains clinically silent for decades
Pathological mass but grow without necessarily displacing functional structures of the brain
Considerable variability in presentation
No two AVMs are alike
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Definition
Congenital, high-flow, high-pressure lesions with the primary risk of devastating intracerebral hemorrhage
Important characteristics: nidus size and locationnumber and locations of arterial feederspattern of venous drainage
Only complete removal offers definitive reduction of bleeding risk
Surgical resection, Radiosurgery, endovascular occlusion or combination approaches used for treatment
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Classification
Vascular malformations are dysplastic processes
And NOT neoplastic (not to be confused with suffix “oma” used in cavernoma, venous angioma etc.)
Traditionally, 4 different entities recognized:
Developmental venous anomalies
Capillary telangiectasias
Cavernous malformations
AVMs – differs from the rest 3: due to AV shunt whereby oxygenated blood passes directly into the venous system without gas exchange
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AVM subtypes:
Plexiform
artery connecting to a network of poorly differentiated, immature vessels before passing into a vein
plexiform network - is termed a nidus (Latin – “nest”)
Fistulous
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Diagnostic Radiology
Cross-sectional Imaging
MRI:
Geometric definition of nidus and its relation to adjacent structure
Hypointense signals on T2 represents flow voids of various feeding arteries, draining veins or vessels within the nidus
Hypointensity peripheral to nidus on gradient echo MRI is suggestive of hemosiderin deposits from subclinical
hemorrhage
MRA and MRV for non invasive delineation of flow though temporal sequencing is lacking
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CT scan (plain)
acute determination of intracranial hemorrhage
25-30% AVMs have calcium deposition – apparent even in the presence of hemorrhage
iso- to hyperdense serpiginous vessels located at some distance from the hemorrhage
helpful to rule in rather than to rule out AVM
CT angiogram – helpful in an unruptured AVM
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Angiography
No cerebral AV shunt can be completely understood without the aid of a selective cerebral angiogram
DSA – subtract out static components of the image (i.e., the skull)
weakness: lack of geometric characterization and
localization of the nidus
feature: early opacification of the nidus or draining veins in the routine arterial phase of the angiogram
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Radiological Findings:
Nidus
size of the AVM = size of the nidus
!!! Confounder = adjacent dilated veins
cross sectional imaging for more accurate measurement as for any mass lesion
location – to see for proximity to eloquent areas IMPORTANT
shape characterization for surgical and radiosurgical planning
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Arterial supply
Noted for number, size, relative contribution to the nidus, location
Which vascular territory they arise from?
Best to describe its course from the Circle of Willis
For large AVMs, if there is concern for meningeal involvement – angiogram of ECA
Contribution from deep perforating artery noted
AVMs in “vascular border zone” as in temporal and occipital lobe: may have supply from both anterior and posterior circulation
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3 types of arterial feeders:
Direct/Terminal feeders – end directly into the nidus
Transit feeders – normal arteries that pass near or even through the nidus while going on to supply normal tissue
can be easily obscured with nidus opacification
eg. Pericallosal artery passing adjacent to mesial frontal lobe nidus before proceeding posteriorly
Indirect feeding or artery en passage – passes near the nidus and contribute to the shunt before continuing on to supply normal brain
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Superselective angiography of suspected vessel
shows if it contributes to the nidusdistinguishes a transit artery
Importance!!! –
embolization or surgical ligation of an unrecognized en passage artery -infarcts of normal tissue
Helps identify intranidal or prenidal aneurysms
Supply of AVM from pial collaterals to be noted
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Venous Drainage
Note for number, size and locations
Unusual character with tortuous course, ectasias, or stenosis
Note the drainage – surperficial (cortical surface) vs deep (Galen)
Important to recognize the possible existence of normal veins draining functional area adjacent to the lesion like “transit artery”
Such veins opacify later than veins draining the nidus on angiogram; though difficult to distinguish intraoperatively
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Special Tests:
Functional MRI (fMRI)
to assess the proximity of language and motor function in relation to AVM
Tractography
aid in assessing the relationship of deep white matter tracts to the AVM
Intraoperative functional mapping – limited value – we cannot do partial treatment as contrast to tumors
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Grading Systems
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Weaknesses of Spetzler Martin Classification
Lacks the ability to assess risks for interventions other than exclusive microneurosurgery
Studies based on highly experienced vascular team and may not necessarily be applicable to a general neurosurgeon’s ability
Interobserver variability can occur
May oversimplify many AVMs
More recent classification attempts at - Deep perforator supply and nidus diffuseness
Flow characterization ?? / posterior fossa AVMs ??
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Weaknesses of Spetzler Martin Classification
Size measurement – linear parameter
Eg. Spherical volume of 5.54 cm diameter AVM – approx. 4 times greater than 3.5 cm AVM; eventhough both assigned 2 points
Treatment with radiosurgery is volume dependent
Volume is a better predictor of microsurgical risk and outcomes
Good point: Simple bedside assessment
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Pathological Sequelae
Hemorrhage
>50% of AVMs – discovered after an ICH
small, deep AVM – intraparenchymal hemorrhage; intraventricular bleed if adjacent to ventricles
cortical AVM – subarachnoid hemorrhage
dAVF may only present with SAH; should be considered in the DDx of non aneurysmal bleed – 6 vessels DSA to be performed on suspicion
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Seizures
Second most common presenting symptom
Associated with supratentorial AVMs
15-30% patients
Cause: cortical irritation or remodeling from ischemia, altered hemodynamics, mass effect or microhemorrhage
Mostly, well controlled with medical management
Similar long-term risk profile for hemorrhage than with other presentations
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Angiographic characteristics of epileptogenic AVMs
cortical location of the nidus or feeding artery (temporal/parietal)
feeding by the MCA or ECAabsence of aneurysms including intranidalpresence of varices in the venous drainage
Subset of patients – medically refractory epilepsy
confirmation of epileptic focus using EEG, MEG, SPECTfollowed by radiosurgery
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Headaches..
Presenting symptom in 15% patients without evidence of rupture
Similar to migraine – lateralization to one side but more permanent
Neurological Deficit..
rare presentation
transient, progressive, or permanent
due to mass effect or arterial steal
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Development of AVM
Congenital – develop during embryonic stage
For: histological characteristics resembling plexuses of developing vasculature in embryo
predisposition in genetic disorders like Osler-Weber-Rendu
Against: recur though rarely, after post treatment angiographic evidence of obliteration by surgery or radiosurgery
?? Whether they occur de novo or develop into larger structures that can eventually be seen radiographically
Points out – dynamic lesion that can develop or remodel over time
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Congenital theory – failure of development of a stable vascular and capillary plexus
Three processes: vasculogenesis, angiogenesis and arteriogenesis play role
Vasculogenesis – creates a haphazard network of immature cells that form angiocysts, which eventually fuse to form a primitive capillary plexus
Angiogenesis – selective apoptosis + migration of supporting vascular smooth muscle cells to form stable vascular bed
Arteriogenesis – plays important role in later growth and remodelling; being mediated by vascular wall shear stress
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Molecular Biology and Genetics..
Altered expression of many factors
~900 genes – altered expression in AVMs
Increased amount of VEGF (Vascular Endothelial Growth Factor)
ANG (angiopoetins) – regulates recruitment of smooth muscle cells and pericytes to endothelial cells
FGFs (Fibroblast Growth Factors) – help differentiate progenitor cells to angioblasts during vasculogenesis
Mutation in HHT1 and HHT2 genes found on chromosome 9q and 12q respectively (Hereditary Hemorrhagic Telangiectasia) – as in OWR synd.
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Physiology..
Categorized into:
Physiology of the malformation itself
Physiology of the surrounding brain
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Physiology within a malformation..
Hemorrhage occurs when the pressure within the vessel wall exceeds the limit for structural integrity
Stress delivered depends on the pressure along with radius and thickness of the vessel
Flow increase – increased arterial pressure, decreased draining pressure, decrease in vascular resistance
Capacitance – ability of the nidus to increase flow without necessarily increasing vascular resistance or therefore pressure
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Concept translated to management:
Decreasing flow is best effected by obstructing feeding arteries
Decreasing flow by obstructing veins will increase intranidal pressures, and therefore, bleeding risk
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Physiology of surrounding brain..
Normal brain can no longer match the low resistance of AV shunt and becomes underperfused “vascular steal”
Vascular beds of normal brain parenchyma perfused at lower local arterial pressures
Surrounding brain develops relatively low vascular resistance
Increased shunting by a low vascular resistance within an AV shunt
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Normal Perfusion Pressure Breakthrough (NPPB)
Becomes hyperemic with increased risk for post resection hemorrhage
Capillary beds not used to higher pressure
Overall systemic resistance increases in response to removal of AVM
Adjacent tissue loses the ability to autoregulate
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N.B. .. Clinical utility from the understanding of this concept..
fMRI used for identifying eloquent area for surgical planning utilizes cerebral blood flow changes at the microcirculatory level to determine functional activation of brain
May produce false report due to disrupted autoregulation
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Epidemiology and Natural Course
Rarity along with long period of clinical silence makes it difficult to estimate the overall prevalence
Incidence: approx. 1 per 1,00,000 person-years
Risk of Rx to be weighed against no intervention (ARUBA trial)
Though rare – might at times show spontaneous regression
Smaller AVM – increased risk of rupture (probably due to higher feeding pressure)
Risk of annual hemorrhage: 2-4%
Combined morbidity and mortality: 2.7%
Mean time to hemorrhage: 7.7 years
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2008 Finnish AVM cohort:
multivarate analysis showed – hemorrhage risk factors to include
previous rupture
infratentorial
deep location
large size
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Cumulative probability of an annualized risk for expected years of remaining life…Cumulative probability p = 105-age/100
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AVM in the Pediatric population..
More morbid sequelae and devastating consequences
Most likely presenting symptom: Hemorrhage
Others: Seizure, congestive heart failure, neurological deficit
CHF – mostly in newborn due to large amount of left to right shuntEg. Vein of Galen Malformation
Surgically resected – occasionally recur – due to microshunting which grows over time
Rx: microsurgical resection with preoperative embolization unless risk of neurological deficit
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AVM and Pregnancy..
Total blood volume increase by 40% and cardiac output by 60%
Arterial pressure can vary: hypertension can occur near delivery
Increased chance of hemorrhage (unclear as if statistically significant)
If pregnant woman presents with a hemorrhage from an AVM, the risk of rebleed during the same pregnancy: ~ 27%
Risk mitigated only with total resection
Rx entails risk to both mother and fetus
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AVM and Pregnancy..
Radiosurgery:
risk to fetus and slow rate of occlusionnot a viable option during pregnancy
Endovascular:
risks of exposing the fetus to radiation, IV contrast and embolic solvents
MICROSURGICAL resection: only tool if patient wishes to have treatment before delivery
In general definitive Rx deferred until the pregnancy is over
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AVM and Pregnancy..
Followed in high risk pregnancy setting and delivered by c-section
Immediate surgical evacuation for stabilization – if life threatening hemorrhage
Careful discussion with family regarding risks of hemorrhage and disability with intervention
Pregnant with unruptured AVM – definitive Rx after parturition
Seizures – controlled with anticonvulsant with minimal teratogenic risk
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AVM and Aneurysms..
Special challenge
Increased flow associated with AVM vessels – predispose to aneurysm formation due to shear stress on vessel wall
4 types:
unrelated to flow vessels (remote)
flow relatedarising at the circle of Willis origin of a vessel supplying the
AVM (proximal)
arising from the midcourse of a feeding pedicle (pedicular)
arising from within the nidus itself (intranidal)
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Aneurysm rupture is a possible clinical consequence
Risk of ruptured aneurysm should be considered
4 vessels angiogram (CTA or MRA) to rule out aneurysm
Risk of morbidity and death from aneurysmal SAH is higher than from AVM
Flow related aneurysms may regress spontaneously after AVM resection
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Few important questions to ask..
Where is the aneurysm?
Which pathological entity was responsible for the hemorrhage?
Is the AVM sufficiently visualized?
If it is well visualized, can it be safely treated surgically?
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AVMs and Aneurysms..
If AVM surgically treatable:
aneurysm secured and both treated in the same setting
If there is doubt as to the resectability of AVM:
treat aneurysm by any means acutely and leave the nidus alone for later, multidisciplinary management
Intranidal aneurysm:can be difficult to visualize in imaging modalitycan be difficult to diagnose it as a cause for bleedingany Rx for AVM, deals with it automatically; hence Rxed
together surgicallyif radiosx being considered; limited endovascular
embolic therapy
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Treatment
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Treatment
If presents with hemorrhage
Rx based on degree of hemorrhage and neurological status
risk of immediate rebleeding is relatively low; hence, early treatment without advanced understanding of the AVM characteristics can rather be dangerous unless a life threatening hematoma requiring immediate surgical evacuation
Rx delayed to allow time for hemorrhage to resolve and the AVM to stabilize its architecture
prompt intervention if neurological deterioration on observation
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EVD if hydrocephalus
Decompression of hematoma while avoiding AVM, if hematoma needs urgent removal
Decompressive craniotomy if brain swelling+
For definitive treatment other options:medical or symptomatic managementembolizationmicrosurgeryradiosurgerymultimodality therapy
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The main considerations for choosing the right option:
Size of AVM
Location
Vascular anatomy
Age
Medical condition
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Medical Management
Indications:
very extensive, deeply located with blood supply primarily from deep perforating vessels not amenable to endovascular or radiosurgical Rx
very advanced age
comorbidities – advanced heart disease, respiratory insufficiency, cancer with metastasis
Rx – AEDs for seizure control
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Embolization
Not considered as exclusive general treatment for most AVMs
rate of permanent morbidity 4-14%
not all vessels of all size and location can be safely embolized and hence, adherence to the goal of complete obliteration of AVM can not be achieved in most instances
reconstitution of shunting by recanalization or de novo vascular development
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Technique of Embolization
Transfemoral access
Microcatheter used to access intracerebral vasculature
Selected feeding arteries isolated
Various agents delivered
Avoid premature venous outflow occlusion, which can cause rupture
Often combined with multimodality approach
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Knowing the goal is important – volume reduction for safe radiosurgery vs. overall flow reduction to reduce blood loss during later microsurgery or embolization of feeding vessel, which is difficult to be accessed during surgery
Complete embolization NPPB
Staged embolization in multiple sessions can be done with ease
Large amount of embolic material stiff AVM difficult mobilization during surgery
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Embolic Agents..
3 categories used:
Occlusive Devicesbraided silk thread/ platinum coils
Particles (45-1180 μm) – appropriate size selection important otherwise lodges in the nidusmixed with contrast before deliveryimportant to note that it does not reflux into the enpassage
artery or normal capillary bedPVA (polyvinyl alcohol)
LiquidsNBCA (N-Butyl cyanoacrylate)/ EVOH (ethylene and vinyl
acohol)
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NBCA
Monomer – stabilized in hydrophobic ethiodol solution
Mixed with tantalum for radioopacity
Chemical variant of superglue – used as fast acting skin adhesive
When comes in contact with blood, polymerizes to form a solid cast
Rate of polymerization, manipulated by varying amount of ethiodol
Important for the use in fast flowing fistulous connection vs. large, plexiform nidus
Caution: to prevent polymer from flowing in the venous circulation risking PE
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EVOH (Ethylene and vinyl alcohol) - Onyx
Copolymer (mixed with tantalum powder and dissolved in DMSO – dimethyl sulfoxide)
Copolymer precipitates and DMSO diffuses in a lava like manner
Outer portion remains nonadhesive but solidifies
Central core – continues to flow
Remains in patient’s system for several days with a distinctive odor
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Timing between Embolization and Surgery
Matter of debate
Should be waited enough for the vascular pedicles to be taken out by embolization
And
Not too long so as there is alteration of hemodynamics of AVM nidus and risk of hemorrhage
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Microsurgery..
Positioning
lesion ideally perpendicular to the surgeon’s line of sight
working corridor as short as possible to allow for minimal retraction and a comfortable working length
gravity as an aide to retraction and drainage
special consideration to the locations of the arterial feeders
larger craniotomy to assist in locating the feeders, as well as having a broader perspective of the malformation
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General Microsurgery Principles..
Consideration of complex nature of feeding arteries and draining veins
First objective: identification of the nidus location – neuronavigation
Attempt to localize all the major feeding arteries
Then disconnecting them with nidus
Ideally, preoperative angiogram to be studied not only to see the location but to plan, in which order will they be encountered during surgery
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General Microsurgery Principles..
Feeding arteries distinguished from draining veinsNOT by sight, but by noting if the distal vessel collapses with
gentle occlusion
Secure the feeder as close to the nidus as possible to ensure there is no en passage artery feeding normal brain
Securing the individual vessels can be done with bipolar coagulation
Coagulation however can be difficult at times due to thin vessel wall and high pressure of blood flow; Sundt vascular microclips may be used
Excessive bipolar usage or premature disconnection can cause vessel to retract within brain parenchyma !!!
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Placing cotton patty with gentle pressure may not work due to high flow
Bipolar should be kept at low power and vessels occluded gradually
Dissection of nidus after securing of artery
Nidus separated from surrounding parenchyma; hemorrhage plane may be a good starting point
Maintain a uniform depth with circumferential separation to avoid encountering a poorly visualized vessel.
Careful not to enter the nidus: difficult hemostasis
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Dynamic nature of the nidus makes it compressible than the surrounding brain with easy surgical manipulation unlike solid tumor
As more feeders are isolated and secured, the intranidal pressure decreases and allow for more manipulation
Deep arteries generally encountered last
Draining veins should be preserved at all cost to avoid an intranidal pressure increase
Often, however impractical, especially if the veins are superficial to the nidus, thereby tethering it in a way that prevents easy manipulation
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Last structure to be secured before removing the nidus are the draining veins
When resecting the nidus, one should exercise caution to note if small feeding arteries are still attached
If intraoperative hemorrhage – need to figure where the hemorrhage is from
If from nidus – cotton ball placed over the location with the least pressure possible to arrest or even slow down the blood loss enough to visualize its source
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If hemorrhage deep from the nidus – inadvisable to explore the nidus itself because of risk of creating multiple hemorrhages that are difficult to control
Surgical assistants should exercise caution with excessive suctioning
Small arterial feeders may retract into the parenchyma, preventing easy visualization
Hemorrhage may be due to NPPB from surrounding parenchyma – manifest first by rapid edema
Blood pressure reduction and packing of the surgical cavity may assist in localizing the hemorrhage
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Surgical approaches..
For Deeper AVMs.. 3 categories
transcortical-transventricular
interhemispheric
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Postoperative Management
Admitted to ICU
Continued arterial blood pressure and neurological checks
Advisable to undergo angiogram to confirm total resection of the AVM prior to discharge
If incomplete resection – reopening craniotomy done during the same admission
Postoperative complications – hemorrhage, seizures, cerebral edema, post-surgical infarcts especially related to venous occlusions
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Radiosurgery..
Goal: delivery of sufficient ionizing radiation to the complete nidus
volume to obliterate AV shunting
Adv:ability to treat without need of craniotomyideal for deep seated AVMs and in patients with comorbiditiesless risk of NPPB or immature venous occlusion
Disadv:considerable delay of 2 to 5 years to show effectno reduction in hemorrhage rate during that timeapplying 2.7% annual risk – corresponds to 5.3-12.7% risk,
which is even more if the AVM has recently bledeffects of radiation: postradiation edema, cyst formation &
radionecrosis
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Mechanism:
inflammatory response to high dose radiation loss of endothelium and proliferation of smooth muscle cells obliteration
18 Gy to the 70% isodose line means:
periphery of the nidus will receive 18 Gy and the interior will receive up to 18/0.7 = 25.7 Gy
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Good predictors of successful AVM obliteration:
Nidus volume less than 3 ml
Nidus smaller than 2 cm in its largest diameter
Sharp delineation of the nidus border on imaging
Younger age
Fewer draining veins
Hemispheric location
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Hemorrhage mass effect distortion of AVM 3 D anatomy inaccurate localization for radiosurgical targetting
4-6 wks of waiting before the nidus achieves a stable geometry – then only radiosurgery to be performed
Conservative definition of radiosurgery failure if persistence of AVM on angiography 5 years after the treatment
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DURAL ARTERIOVENOUS FISTULAS
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Introduction..
Aka Dural AVMs
Acquired lesions and NOT congenital
Most dAVFs occur adjacent to the venous sinuses
dAVF – shunting between the arterial vessels supplying the dura and the sinuses
Mostly idopathic
Inability of spontaneous thrombosis of the high flow fistula due to low pressure of the adjacent venous drainage
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Adjacent venous sinus thrombosis rather may be the triggering factor
Thrombosis leads to opening up of microvessels within the sinus and also the release of pro-angiogenesis factors.
Biologically active – can recruit additional arterial supply
Rarer than AVM
Most common region – transverse and sigmoid sinuses
Other locations – cavernous, straight, petrosal and SSS
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Carotid Cavernous fistula Type B,C and D are types of dAVFMay be formed due to trauma or rupture of cavernous carotid aneurysm
CCFA – direct communication between ICA and
cavernous sinus
B – meningeal ICA branches and cavernous sinus
C – meningeal ECA branches and cavernous sinus
D – meningeal branches of both ICA /ECA and cavernous sinus
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Main morbidity – ICH risk
Do not have well defined nidus
Anatomical presentation influences the risk of rupture
Mechanical strength of dural sinuses withstand arterial pressure more than the intracranial vein minimal risk of rupture than if cortical vein is involved
Basis of Borden and Cognard Classification system
Borden is simpler but Cognard’s advantage over Borden is the use of flow dynamics based on angiography
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Other clinical findings:
Bruit/ pulsatile tinnitus/ headache/ papilledema/ seizures/ neurological deficit
CCF – increased IOP visual deficits emergent therapy
Papilledema and features of raised ICP is due to thrombosis of sinus associated in majority of cases
Routine MRI and MRA miss the lesion unless of significant size
It is critical to distinguish sinus drainage vs cortical venous drainage
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Selective and superselective angiography including the external carotids and vertebral arteries – required for distinction
Rx – Type I with benign symptoms – observationDebilitating tinnitus – operation
Sinus resection (transverse sigmoid sinus) or even bone may be required
Endovascular or microsurgical techniques to occlude the feeders
Unusual anastomosis between ECA and ICA branches require identification to avoid inadvertent passage of embolic material into the IC circulation, risking neurological deficits
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Thank you!!