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Pial Arteriovenous Malformations
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ac
d
Fig. 3.20a–e. Brain AVM with a high fl ow fi stulous compartment (arrow). Elimination of the fi stula (arrowhead) with coils
and Onyx could be achieved during proximal fl ow interruption using a microballoon (Hyperglide, MTI)
b
e

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C. Cognard, L. Spelle, and L. Pierot
a
c
b
Fig. 3.21a–d. Temporal small brain AVM with superfi cial
venous drainage in a patient with seizures. Complete obliteration with Onyx could be achieved; the Onyx cast demonstrates penetration of Onyx into the proximal part of the
vein (arrow)
fl ow and to achieve stasis to be able to inject Onyx or
a combination of coils and Onyx (Fig. 3.24).
Onyx has some advantages and some drawbacks
to its use in AVMs:
Advantages
The major advantage to the use of Onyx compared
with cyanoacrylates is the ease of injection. The
catheter should be placed in the same wedge situation as for intranidal glue injection. The injection
should be very slow, as well. It may be stopped for
d
a few seconds or minutes to wait for precipitation
of Onyx in order to avoid refl ux, and then resumed.
Control angiography may be performed during
Onyx injection for a better understanding of material progression and of nidus and vein occlusion.
Onyx always behaves as a column, and the formation
of small drops fl owing into the vein that may be seen
when glue is injected too fast normally do not occur.
In a brain AVM associated with a high fl ow fi stula
passover of Onyx into the venous system might occur. In such a condition, high concentration Onyx
(Onyx 34) should be used sometimes necessarily in

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a
c
b
d
Fig. 3.22a–e. Small infratentorial brain AVM with two as-
sociated aneurysms along the PICA in a patient with SAH.
Complete endovascular cure could be performed while coiling the proximal aneurysm and embolising the AVM with
Onyx through the superior cerebellar artery. Note: after
AVM-treatment the more distal aneurysm disappeared
e

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C. Cognard, L. Spelle, and L. Pierot
a
b
c
d
e
f

Pial Arteriovenous Malformations
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Fig. 3.23a–h. Large occipital brain AVM in a patient with
longstanding migraine and learning problems. This AVM
(Spetzler grade IV) could be completely obliterated with
Onyx in two sessions. 3 month control showed stable occlusion of the AVM, the migraine was completely gone
109
h
association with proximal fl ow reduction, e.g. with
adjunct microballoon. The injection may last for
several minutes or even tens of minutes. The total
amount of Onyx injected at one time in one single
pedicle may therefore be much more than with glue.
It reduces the number of catheters used and the total
number of procedures needed to achieve a complete
cure of the AVM. The other major advantage is that
because injection is more prolonged and the decision to stop or continue the injection does not have
to be made immediately, as it does for g lue injection,
the training of young neuroradiologists to perform
Onyx injection is much easier than the mastering
of glue injection.
Disadvantages
The toxicity of DMSO has been discussed in a few
reports (Chaloupka et al. 1994; Sampei et al. 1996;
Murayama et al. 1998; Chaloupka et al. 1999). The
fi rst paper of Chaloupka and coworkers emphasized
the risk of severe vasospasm after injection of 0.8 ml
EVOH and DMSO in the swine rete mirabile with
subsequent infarction. Injection of 0.5 ml resulted in
delayed (7–14 days) subarachnoid hemorrhage with
angionecrosis on histology and arterial microaneurysms. Two other studies reexamined this toxicity
and concluded that the two major points are contact
time with the arterial wall and volume of injection
(Murayama et al. 1998; Chaloupka et al. 1999).
Finally, it has been proved that injection of 0.3 ml for
40 s produced neither vasospasm nor angionecrosis.
The protocol of injection is as follows: Prior to injection the microcatheter is fl ushed with 5 ml normal
saline. Then 0.25 ml DMSO is injected over more
than 40 s for dead space catheter fi ll ing. Ony x i s then
injected slowly (Jahan et al. 2001). Nevertheless,
despite the fact that this protocol was used in all the
23 patients treated, histology showed angionecrosis
of many vessels in two of four patients operated on
1 day after embolization. Consequently, there is still
some question of a likely toxicity of DMSO. One issue may be that because of the wedge position of the
catheter, there might be a stagnation of DMSO in the
pedicle and nidus, with prolonged contact of DMSO
with the vessel wall and risk of necrosis.
At the beginning of injection there is frequently a
refl ux of Onyx along the tip of the catheter. The injection must be stopped and resumed a few seconds
or minutes later until a progression within the nidus
is observed. As soon as it has precipitated around
the tip of the catheter, Onyx tends to open different
compartments of the nidus and the injection may be
prolonged. This technique carries two risks: the oc-

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a b
Fig. 3.24a–d. Temporo-frontal brain AVM (Spetzler grade III) in a very eloquent area in a 36-year-old patient with a hem-
orrhage a year ago clinically associated with transient speech problems. Preoperative tremendous nidal reduction could
be achieved in two sessions using Onyx. After resection of the residual nidus the patient was neurologically intact without
any speech problems
clusion of an adjacent normal branch due to refl ux
of Onyx in the feeding pedicle; gluing of the tip of
the catheter because of a very prolonged injection.
Although Onyx is not adhesive, catheter withdrawal
may be diffi cult and result in either gluing or breaking of the catheter, or stretching and rupture of the
AVM and artery. Attachment of the catheter is due to
physically clutching the microcatheter, if that condition occurs it is important to withdraw the catheter very slowly under continuous gentle pulling. In
the posterior circulation this may result in very low
heart frequency until asystolie. Pushing back the
microcatheter will immediately recover heart beat
and the manoeuvre should be redone. But in general, very prolonged injection with serious refl ux
more than 1.5 cm along the catheter tip should be
unconditionally avoided.
One of the major advantages of Onyx is that a
large volume may be introduced in one single catheter injection. However, there is a risk of hemorrhage.
The operator may be temped to occlude a very large
portion of the nidus in one procedure. Many years
ZZ

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c
ago it was proven that staged embolization aimed at
reducing the nidus in several sessions is mandatory
to progressively modify the fl ow dynamics. Very
sudden and large-scale occlusion of the nidus surely
increases the risk of postprocedural hemorrhage, as
discussed above.
There are still two situations in which Onyx
should not be used today: direct fi stula, in which
the Onyx cannot occlude solely a high-fl ow large
shunt because it is not adhesive, and a feeding pedicle “en passage”, in which refl ux on the tip of the
d
catheter is not allowed due to major risk of normal
vessel occlusion like in any other liquid embolic
material. But if the “en passage-vessel” could be
catheterized far enough slowly injection of Onyx
might be possible and other compartments of the
nidus could be reached from this position. A very
important point is that one should be aware of the
amount of refl ux. To avoid extensive amount of refl ux the concept is to wait and plug the “way back”
which can take some minutes but time investment
is justifi ed.

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C. Cognard, L. Spelle, and L. Pierot
3.5.4
Therapeutic Strategy
It is extremely diffi cult to establish a therapeutic
algorithm for brain AVM. The indication for treatment basically depends on:
Clinical presentation (hemorrhage or not)
Patient age
Natural risk, roughly evaluated by the presence
or not of likely risk factors of bleeding (associated
aneurysm or false aneurysm, venous stenosis or
ectasia)
AVM size, location (superfi cial or deep, eloquent
or not) and angioarchitecture (compact or diffuse)
The goal of treatment may be:
Defi nitive complete obliteration to protect from
hemorrhage
Partially targeted treatment (embolization) to
eliminate risk factors of bleeding/rebleeding
(feeding artery aneurysms, intranidal aneurysms,
false aneurysms)
Partial treatment in case of AVM presenting with
worsening neurologic defi cits (although the effi cacy of such treatment is yet to be proven)
Partial treatment should not be performed to:
Decrease bleeding risk, because even subtotal
therapy does not confer protection from hemorrhage
Improve seizures, because of treatment-induced
risks and unproved effi ciency
The indication for treatment, goal of treatment,
and therapeutic strategy should be decided on by an
experienced multidisciplinary team in agreement
with the patient, who has been precisely informed of
natural and therapeutic risks. Multimodality treatment is frequently performed – either as a planned
maneuver, typically with embolization followed by
radiosurgery or surgery, or as an unplanned maneuver when one modality fails and a second modality
is required for complete obliteration. Goals of the
different modalities should be clear at the outset. In
our experience, embolization is the fi rst-intention
approach in the vast majority of the patients, followed by either surgery or radiosurgery. Nevertheless, because of the extreme variability of resources
available in any one area of the country or world, as
well as very different skills and experience on the
part of neurosurgeons and interventional neurora-
diologists, it is impossible to draft any recommendations about strategy itself. Because there is almost
never a need for brain AVM treatment in emergency
(as opposed to aneurysm treatment), patients with
brain AVMs should be sent to very specialized and
experienced centers that can afford the most up-todate multimodality therapy.
Acknowledgements go to Drs. Zhang Peng and Zhu
Fengshiu for their major contribution to the bibliographic research.
References
Aberfeld DC, Rao KR (1981) Familial arteriovenous malfor-
mation of the brain. Neurology 31:184–186
Aesch B, Lioret E, deToffel B et al. (1991) Multiple cerebral
angiomas and Rendu-Osler-Weber disease: case report.
Neurosurgery 29:599–602
Akin ED, Perkins E, Ross IB (2003) Surgical handling char-
acteristics of an ethylene vinyl alcohol copolymer compared with N-butyl cyanoacrylate used for embolization
of vessels in an arteriovenous malformation resection
model in swine. J Neurosurg 98(2):366–370
Alkadhi H, Kollias SS, Crelier GR et al. (2000) Plasticity of
the human motor cortex in patients with arteriovenous
malformations: a functional MR imaging study. AJNR
Am J Neuroradiol 21:1423–1433
Al-Rodhan NRF, Sundt TM Jr, Piepgras DG (1993) A theory
for the hemodynamic complications following resection
of intracerebral arteriovenous malformations. J Neurosurg 78:167–175
Al-Shahi R, Warlow C (2001) A systematic review of the fre-
quency and prognosis of arteriovenous malformations of
the brain in adults. Brain 124:1900–1926
Amin-Hanjani S, Robertzon R, Arginteanu MS, Scott RM
(1998) Familial intracranial arteriovenous malformations. Case report and review of the literature. Pediatr
Neurosurg 29:208–213
Andrews BT, Wilson CB (1987) Staged treatment of arte-
riovenous malformations of the brain. Neurosurgery
21:314–323
Aoki Y, Nakasawa K, Tago M et al. (1996) Clinical evaluation
of Gamma knife radiosurgery for intracranial arteriovenous malformations. Radiat Med 14:265–268
Aoki S, Sasaki Y, Machida T et al. (1998) 3D-CT angiogra-
phy of cerebral arteriovenous ma lformations. Radiat Med
16:263–271
Bank WO, Kerber CW, Cromwell LD (1981) Treatment of in-
tracerebral arteriovenous malformations with isobutyl
2-cyanoacrylate: initial experience. Radiolog y 31:1
Barnett GH, Little JR, Ebrahim ZY, Jones SC, Friel HT (1987)
Cerebral circulation during arteriovenous malformation
operation. Neurosurgery 20:836–842
Batjer HH, Suss RA, Samson D (1986) Intracranial arterio-
venous malformations associated with aneurysms. Neurosurgery 18:29–35

Pial Arteriovenous Malformations
https://t.me/med1917
113
Batjer HH, Devous MD Sr, Meyer YJ, Purdy PD, Samson DS
(1988) Cerebrovascular hemodynamics in arteriovenous
malformation complicated by normal perfusion pressure
breakthrough. Neurosurgery 22:503–509
Batjer HH, Devous MD Sr, Seibert GB et al. (1989a) Intracra-
nial arteriovenous malformation: relationship between
clinical factors and surgical complications. Neurosurgery
24:75–79
Batjer HH, Purdy PD, Giller CA, Samson DS (1989b) Evidence
of redistribution of cerebral blood fl ow during treatment
for an intracranial arteriovenous malformation. Neurosurgery 25:599–605
Berenstein A, Choi IS (1988) Surgical neuroangiography of
intracranial lesions. Radiol Clin North Am 26:1143–1151
Berenstein A, Lasjaunias P (1992) Classifi cation of brain arte-
riovenous malformations. In: Surgical neuroangiography,
vol 4. Springer, Berlin Heidelberg New York, pp 1–86
Berg JN, Gallione CJ, Stenzel T et al. (1997) The activ in recep-
tor-like-kinase 1 gene: genomic structure and mutations
in hereditary hemorrhagic telangiectasia type 2. Am J
Hum Genet 61:60–67
Berman MF, Sciacca RR, Pile-Spellman J et al. (2000) The
epidemiology of brain arteriovenous malformations.
Neurosurgery 47:389–396
Bert helsen B, Lofgren J, Svendsen P (1990) Emboli zation of ce-
rebral arteriovenous malformations with bucrylate: experience in a fi rst series of 29 patients. Acta Radiol 31:13–21
Betti OO, Munari C (1992) Traitement radiochirurgical avec
accélérateur linéaire des “petites” malformations artérioveineus intra-craniennes. Neurochirurgie 38:27–34
Betti OO, Munari C, Rosler R (1989) Stereotactic radiosur-
gery with linear accelerator: treatment of arterio-venous
malformations. Neurosurgery 24:311–321
Binder JR, Swanson SJ, Hammeke TA et al. (1996) Determi-
nation of language dominance with fMRI: a comparison
with the Wada test. Neurology 46:978–984
Blat DR, Friedman WA, Bova FJ (1993) Modifi cations based
on computed tomographic imaging in planning the radiosurgical treatment of arterio-venous malformations.
Neurosurgery 33:588–595
Brown RD, Wiebers DO, Forbes G et al. (1988) The natural
history of unruptured intracranial arteriovenous malformations. J Neurosurg 68:352–357
Brown RD, Wiebers DO, Forbes GS (1990) Unruptured intra-
cranial aneurysms and arteriovenous malformations and
relationship of lesions. J Neurosurg 73:859–863
Brown RD Jr, Wiebers DO, Torner JC, O’Fallon WM (1996a)
Incidence and prevalence of intracranial vascular malformations in Olmsted County, Minnesota, 1965 to 1992.
Neurology 46:949–952
Brown RD Jr, Wiebers DO, Torner JC et al. (1996b) Frequency
of intracranial hemorrhage as a presenting symtom and
subtype analysis: a population-based study of intracranial vascular malformations in Olmsted Country, Minnesota. J Neurosurg 85:29–32
Carpentier AC, Constable RT, Schlosser MJ et al. (2001) Pat-
terns of functional magnetic resonance imaging activation in association with structural lesions in the rolandic
region: a classifi cation system. J Neurosurg 94:946–954
Carter LP, Gumerlock MK (1995) Steal and cerebral arterio-
venous malformations. Stroke 26:2371–2372
Castel JP, Kantor G (2000) Postoperative morbidity and mor-
tality after microsurgical exclusion of cerebral arteriove-
nous malformations. Current data and analysis of recent
literature. Neurochirurgie 47:369–383
Challa VR, Moody DM, Brown WR (1995) Vascular malfor-
mations in the cent ral nervous system. J Neuropathol Exp
Neurol 54:609–621
Chaloupka JC, Vinuela F, Vinters HV, Robert J (1994) Tech-
nical feasibility and histopathologic studies of ethylene
vinyl copolymer (EVAL) using a swine endovascular embolization model. AJNR Am J Neuroradiol 15:1107–1115
Chaloupka JC, Huddle DC, Alderman JJ et al. (1998) Classi-
fi cation of vascular malformations of the central nervous
system. J Neuropathol Exp Neurol 54:609–621
Chaloupka JC, Huddle DC, Alderman J et al. (1999) A reex-
amination of the angiotoxicity of superselective injection
of DMSO in the swine rete embolization model. AJNR Am
J Neuroradiol 20:401–410
Cheifetz S, Bellon T, Calles C, Vera S et al. (1992) Endoglin
is a component of the transforming growth factor-beta
receptor system in human endothelial cells. J Biol Chem
267:19027–19030
Chen JW, Kerber C, Hoi-Sang U (1991) Spontaneous regres-
sion of large bilateral basal ganglia arteriovenous malformations. AJNR Am J Neuroradiol 12:835–837
Chin LS, Raffel C, Gonzalez-Gomez I, Giannotta SL, Mc-
Comb JG (1992) Diffuse arteriovenous malformations: a
clinical, radiological and pathological description. Neurosurgery 31:863–868
Cognard C, Weill A, Tovi M, Castaings L et al. (1999) Treat-
ment of distal aneurysms of the cerebellar arteries by intra-aneurysmal injection of glue. AJNR Am J Neuroradiol
20:780–784
Colombo F (1989) Linear accelerator radiosurgery. A clinical
experience. J Neurosurg Sci 33:123–125
Colombo F, Benedetti A, Pozza F et al. (1989) Linear accel-
erator radiosurgery of cerebral arteriovenous malformations. Neurosurgery 24:833–840
Colombo F, Pozza F, Chierego G et al. (1994) Linear accel-
erator radiosurgery of cerebral arteriovenous malformations: an update. Neurosugery 34:14–21
Crawford M, West CR, Chadwick DW et al. (1986) Arteriove-
nous malformations of the brain: natural history in unoperated patients. J Neurol Neurosurg Psychiatr y 49:1–10
Cunha e Sa MJ, Stein BM, Solomon RA et al. (1992) The treat-
ment of associated intracranial aneur ysms and arteriovenous malformations. J Neurosurg 77:853–859
Davis C , Symon L (1985) The ma nagement of cerebral a rterio-
venous malformations. Acta Neurochir (Wien) 74:4–11
De br un G, L ac our P, Ca ron JP et al . (19 78) De tac ha ble ba ll oon
and calibrated leak balloon techniques in the treatment
of cerebral vascular lesions. J Neurosurg 49:635–649
Debrun G, Vinuela F, Fox A et al. (1982) Embolization of
cerebral arteriovenous malformations with bucrylate.
J Neurosurg 56:615–627
Debrun GM, Aletich V, Ausman JI et al. (1997) Embolization
of nidus of brain arteriovenous malformations with n
butyl cyanoacrylate. Neurosurger y 40:112–121
De Oliv eira E, Ted es chi H , Si que ir a MG e t a l. (1 997) Ar ter iov e-
nous malformations of the basal ganglia region: rationale
for surgical management. Acta Neurochir 139:487–506
Deruty R, Mottolese C, Soustiel JF, Pelissou-Guyotat I (1990)
Association of cerebral arteriovenous malformation and
cerebral aneurysm. Diagnosis and management. Acta
Neurochir (Wien) 107:133–139
-

114
https://t.me/med1917
C. Cognard, L. Spelle, and L. Pierot
Deruty R, Pelissou-Guyotat I, Mottolese C, Amat D et al.
(1996) Therapeutic risk in multidisciplinary approach of
cerebral arteriovenous malformations. Neurochirurgie
42:35–43
Deveikis JP, Manz HJ, Luessenhop AJ et al. (1994) A clinical
and neuropathologic study of silk suture as an embolic
agent for brain arteriovenous malformation. AJNR Am J
Neuroradiol 15:263–271
Dias MS , Sekhar LN (1990) Intr acrania l hemorrhage from an -
eurysms and arteriovenous malformations during preg-
nancy and the puerperium. Neurosurgery 27:855–866
Drake CG, Friedman AH, Peerless SJ (1986) Posterior fossa
arteriovenous malformations. J Neurosurg 64:1–10
Duckwiler GR, Dion JE, Vinuela F, Jabour B, Martin N, Bent-
son J (1990) Intravascular microcatheter pressure moni-
toring: experimental results and early clinical evaluation.
AJNR Am J Neuroradiol 11:169–175
Duckw iler GR, Dion JE, Vinuela F et a l. (1992) Delayed venous
occlusion fol lowing embolotherapy of vascular malforma-
tions in the brain. AJNR Am J Neuroradiol 13:1571–1579
Ducreux D, Trystram D, Oppenheim C et al. (2001) Imagerie
diagnostique des malformations artério-veineuses céré-
brales. Neurochirurgie 47:190–200
Duffner F, Ritz R, Bornemann A, Freudenstein D, Wiendl H,
Siekmann R (2002) Combined therapy of cerebral arterio-
venous malformations: histological dif ferences between a
non-adhesive liquid embolic agent and n-butyl 2-cyano-
acrylate (NBCA). Clin Neuropathol 21(1):13–17
Duong DH, Young WL, Vang MC et al. (1998) Feeding artery
pressure and venous drainage pattern are primary de-
terminants of hemorrhage from cerebral arteriovenous
malformations. Stroke 29:1167–1176
Edelman RR, Wentz KU, Mattle HP et al. (1989) Intracerebral
arteriovenous malformations: evaluation with selective
MR angiography and venography. Radiology 173:831–837
Essig M, Wenz F, Schoenberg SO et al. (2000) Arteriove-
nous malformations. Assessment of gliotic and ischemic
changes with fl uid-attenuated inversion-recovery MRI.
Invest Radiol 35:689–694
Farb RI, McGregor C, Kim JK et al. (2001) Intracranial arte-
riovenous malformations: real-time auto-triggered ellip-
tic centric-ordered 3D gadolinium – enhanced MR angi-
ography – initial assessment. Radiology 220:244–251
Fink GR (1992) Effects of cerebral angiomas on perifocal and
remote tissue: a multivariate positron emission tomogra-
phy study. Stroke 23:1099–1105
Finnerty JJ, Chisholm CA, Chapple H et al. (1999) Cerebral
arteriovenous malformation in pregnancy: presentation
and neurologic, obstetric, and ethical signifi cance. Am J
Obstet Gynecol 181:296–303
Fischer AW, Er H (1930) Lokales Amyloid im Gehirn. Eine
Spätfolge von Roentgenbestrahlungen. Dtsch Z Chir
227:475–483
Folkow B, Gurevich M, Hallbach M, Lundgren Y et al. (1971)
The hemodynamic consequences of regiona l hypotension
in spontaneously hy pertensive and normotensive rats.
Acta Physiol Scand 83:532–541
Fong GH, Rossant J, Gertsenstein M, Breitman ML (1995)
Role of the Flt-1 receptor tyrosine kinase in regulating the
assembly of vascular endothelium. Nature 376:66–70
Fournier D, Terbrugge K, Rodesch G et al. (1990) Revascular-
ization of brain arteriovenous malformations after em-
bolization with bucrylate. Neuroradiology 32:497–501
Fournier D, Terbrugge K, Willinsky R et al. (1991) Endovas-
cular treatment of intracerebral arteriovenous malformations: experience in 49 cases. J Neurosurg 75:228–233
Fox AJ (1997) Recurrent AVMs after negative angiography.
J Neurosurg 86:170–171
Fox AJ, Pelz DM, Lee DH (1990) Arteriovenous malforma-
tions of the brain: recent results of endovascular therapy.
Radiology 177:51–57
Freeny PC, Mennemeyer R, Kidd CR (1979) Long-time ra-
diographic pathologic follow-up of patients treated with
visceral transcatheter occlusion using isobutyl 2-cyanoacrylate (bucrylate). Radiology 132:51–60
Freudenstein D, Duffner F, Ernemann U et al. (2001) Recur-
rence of a cerebral arteriovenous malformation after surgical excision. Cerebrovasc Disc 11:59–64
Friedman WA, Bova FJ, Mendenhall WM (1995) Linear accel-
erator rad iosurgery for ar terio-venous ma lformations . The
relationship of size to outcome. J Neurosurg 82:180–189
Friedman WA, Blatt DL, Bova FJ et al. (1996) The risk of
hemorrhage after radiosurgery for arterio-venous malformations. J Neurosurg 84:912–919
Frishberg BM (1997) Neuroimaging in presumed primary
headache disorders. Semin Neurol 17:373–382
Frizzel RT, Fisher WS (1995) Cure, morbidity, and mortality
associated with embolization of cerebral arteriovenous
malformations: a review of 1246 patients in 32 series over
a 35-year period. Neurosurgery 37:1031–1040
Fry D (1968) Acute vascular endothelial changes associ-
ated with increased blood velocity gradients. Circ Res
22:165–197
Fults D, Kelly DL (1984) Natural history of arteriovenous
malformations of the brain: a clinical study. Neurosurgery 15:658–662
Gallina P, Merienne L, Meder JF et al. (1998) Failure in radio-
surgery treatment of cerebral arteriovenous malformations. Neurosurgery 2:996–1004
Gao E, Young WL, Pile-Spellman J et al. (1997) Cerebral ar-
teriovenous malformations feeding artefact aneurysms: a
theoretical model of intravascular pressure changes after
treatment. Neurosurgery 41:1345–1356
Garcia-Monaco R, Rodesch G, Alvarez H et al. (1993) Pseu-
doaneurysms within ruptured intracranial arteriovenous
malformations: diagnosis and early endovascular management. AJNR Am J Neuroradiol 14:315–321
Garretson HD (1985) Intracranial arteriovenous malforma-
tions. In: Wilkins RH, Rengachary SS (eds) Neurosurgery.
McGraw-Hill, New York, pp 1448–1457
Germano IM, Davis RL, Wilson CB, Hieshima GB (1992) His-
topathological follow-up study of 66 cerebral arteriovenous malformations after therapeutic embolization with
polyvinyl alcohol. J Neurosurg 76:607–614
Goto K, Uda K, Ogata N (1991) Embolization of cerebral ar-
teriovenous malformations (AVMs): material selection,
improved technique, and tactics in the initial therapy of
cerebral AVMs. Neurol Med Chir (Tokyo) 33(Suppl):193–
199
Graf CJ, Perret GE, Torner JC (1983) Bleeding from cerebral
arteriovenous malformations as part of their natural history. J Neurosurg 58:331–337
Griffi ths PD, Hoggard N, Warren DJ et al. (2000) Brain arte-
riovenous malformations: assessment with dynamic MR
digital subtraction angiography. AJNR Am J Neuroradiol
21:1892–1899
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