Neurosurg Rev (2013) 36:541–549 DOI 10.1007/s10143-013-0470-1 ORIGINAL ARTICLE Sylvian fissure arteriovenous malformations: long-term prognosis and risk factors Lingtong Liu & Hao Li & Jian Zheng & Shuo Wang & Jizong Zhao & Yong Cao Received: 16 July 2012 / Revised: 10 January 2013 / Accepted: 10 March 2013 / Published online: 5 May 2013 # Springer-Verlag Berlin Heidelberg 2013 Abstract Background and objective: Sylvian fissure arteriovenous malformations (AVMs) are among the most challenging AVMs to manage surgically. The estimates of their risk factors and prediction of their long-term prognosis are crucial for clinical decision-making. The authors conducted a retrospective review to patients with sylvian AVMs treated microsurgically to evaluate the risk factors associated with long-term prognosis. Methods: Forty-one patients with sylvian fissure AVMs treated microsurgically between June 2009 and December 2011 were retrospectively reviewed with a mean follow-up time of 23 months (range 6–35 months). Chi-square test was utilized to compare proportions and ranksum test to compare ordinal materials. Odds ratios (ORs) were used to assess risk factors associated with postoperative shortterm outcome and long-term adverse outcome (mRS scores 3– 6). Results: One patient died in 1 month after surgery. Eighteen (43.9 %) patients had postoperative transient neurological deterioration. Good outcomes (mRS scores 0–2) were observed in 29 (72.5 %) patients in the follow-up. From the multiple logistic regression, a history of AVM bleeding and L. Liu : H. Li : J. Zheng : S. Wang : J. Zhao : Y. Cao (*) Department of Neurosurgery, Beijing Tiantan Hospital, Capital Medical University, 6 Tiantan XiliChongwen District Beijing 100050, China e-mail: caoyong6@hotmail.com L. Liu e-mail: liulingtong21@yahoo.com.cn H. Li e-mail: handanlihao-1@163.com J. Zheng e-mail: neurosurgeon.zheng@gmail.com S. Wang e-mail: captain9858@vip.sina.com J. Zhao e-mail: zhaojz205@hotmail.com deep venous drainage increase the risk of postoperative transient neurological deterioration, with OR=8.211 and OR= 4.869, respectively. A history of AVM bleeding was a risk factor for long-term adverse outcome, with OR=7. Conclusions: Despite different Sugita classification subtypes, sylvian fissure AVMs’ long-term results with microsurgical resection are better than expected; a history of AVM bleeding is a risk factor for postoperative temporary neurological deterioration and for long-term adverse outcome, while the AVM deep venous drainage is a risk factor only for temporary neurological deterioration. Keywords Arteriovenous malformation . Sylvian fissure . Prognosis . Risk factors Introduction Sylvian fissure arteriovenous malformations (AVMs) were first described by Kenichiro Sugita in 1987 [1], which is supposed to account for approximate 8.92–11.1 % of all brain AVMs [7, 13]. The reported incidence rates of newly diagnosed AVMs have varied in different population-based studies from 0.89 to 1.34 cases per 100,000 person-years [1, 2, 4, 5, 12]. Based on the data, the incidence rates of newly diagnosed sylvian AVMs varied about 0.09 to 0.14 cases per 100,000 person-years. The sylvian AVMs are among of the most challenging AVMs to manage surgically. They involve the middle cerebral artery and are surrounded by critical structures such as insular cortex, basal ganglia, internal capsule along the deep margin, and Broca’s areas along the lateral margins in the dominant hemisphere. They require substantial subarachnoid dissection to open the sylvian fissure, expose the nidus, and identify feeding arteries and draining veins. Transit arteries that continue beyond the AVM to supply normal brain can resemble feeding arteries 542 and must also be preserved. Draining veins often cover the nidus and need to be preserved throughout the resection. Smaller arteries such as the lenticulostriate and anterior choroidal arteries contribute to these AVMs and can be difficult to expose and control [7]. For its rarity and surgical difficulty, this disease is confined to small series and few studies has yet been able to demonstrate long-term prognosis and associated risk factors [7, 13, 15, 16]. We retrospectively reviewed 41 patients suffering from sylvian fissure AVMs in our hospital and identified their long-term prognosis and prognostic risk factors. Neurosurg Rev (2013) 36:541–549 1.56:1, with 25 males (61 %) and 16 females (39 %). Sixteen (39 %) patients presented with previous hemorrhage before surgery, 16 (39 %) with seizures, 7 (17.1 %) with headaches, and 2 (4.9 %) with hemiparesis. The detail of every patient was shown in the Table 1. In our series, only one patient (patient 40) had ever received endovascular embolization for right lateral sylvian fissure AVM found by intracerebral hemorrhage 8 years ago. She suffered recurrent hemorrhage on the same location before admitted. No other therapy was applied preoperatively and postoperatively in our patients. AVM characteristics Subjects and methods Study population A total of 355 patients with AVMs were treated with microsurgical resection by a single neurosurgeon (SW) at the Beijing Tiantan Hospital, Capital Medical University between June 2009 and December 2011. Of these patients, 41 were identified as having sylvian fissure AVMs. They accounted for 11.55 % of all AVM patients. The study was approved by the Ethics Committee of the Beijing Tiantan Hospital. Cerebral angiography, computed tomography (CT), and/or magnetic resonance imaging (MRI) was performed in all patients to confirm the AVM diagnosis. AVMs were categorized by the operating neurosurgeon as pure, medial, lateral, and deep types, according to the Sugita classification [13]. CT scans, MRI scans, angiograms, intraoperative photographs, and operative reports were reviewed before making these determinations. Follow-up checkups were in 3 to 6 months after the surgery and then at yearly intervals. The most recent checkup was done in the June 2012; mean follow-up time was 23 months (range 6–35 months). Neurological assessments were performed by a neurosurgeon resident, under the supervision of an attending neurosurgeon, preoperatively, postoperatively, and during the follow-up period. Newly emerging neurological dysfunction or deterioration of original neurological deficit appeared shortly after operation (within 1 week) was defined as bad short-term result; no new neurological dysfunction or mitigation of original neurological deficit after surgery was regarded as good shortterm result. The modified Rankin Scale (mRS) [14] was used to grade long-term outcomes. The mRS scores 3–6 was named as bad long-term outcome; mRS scores 0–2 were named as good long-term outcome. Patient characteristics Of 41 patients with sylvian fissure AVMs, the average age was 36.1 years (range, 6–56 years) and the male/female ratio was According to the Spetzler–Martin grading system, 4 patients (9.8 %) were grade I AVMs, 15 (36.6 %) were grade II AVMs, 19 (46.3 %) were grade III AVMs, 2 (4.9 %) were grade IV AVMs, and 1 (2.4 %) were grade VAVMs. The mean diameter of AVMs was 39.7 mm (range, 5–70 mm). Twenty (48.8 %) AVMs located in the eloquent area like Broca gyrus, basal ganglia, and Wernicke’s areas. Thirteen (31.7 %) had deep venous drainages. According to the Sugita classification system, 7 AVMs (17.1 %) were pure AVMs, 17 (41.5 %) were lateral AVMs, 12 (29.3 %) were medial AVMs, and 5 (12.2 %) were deep AVMs. Statistical analyses Frequencies were used for prevalence data. Chi-square test was utilized for categorized data and rank-sum test for ordinal materials. The level of statistical significance for univariate analysis was set at 0.05. The P values for entry and removal during multivariate logistic regression (forward LR) were 0.10 and 0.05, respectively. As for multivariate logistic regression models, we assigned bad result (short or long term) as digit one and good result (short or long term) as digit zero. Odds ratios (ORs) were used to evaluate the strength of association between risk factors and short-term or long-term outcome. All statistical analyses were performed with SPSS software (version: PASW Statistics 18, 2009). Results Surgical outcome All AVMs were exposed with standard pterional craniotomies. Complete removal of the AVM was documented by intraoperative ultrasound and/or confirmed by postoperative angiography in 40 patients, except 1 patient had tight adhesion between the nidus and the middle cerebral artery and failed to be removed completely. One patient suffered from postoperative surgical site intracerebral hemorrhage and then evacuation of hematoma was performed. On the 15th day after operation, this patient died from brain stem Age (year) /sex 54/M 48/M 13/F 27/F 31/M 52/M 35/M 47/M 52/M 45/M 38/M 52/M 47/M 36/M 31/M 48/M 34/F 40/F 7/M 11/M 34/F 34/M 18/F 9/M 43/F 23/F 35/F 19/F 7/F 20/M 42/M 48/F 11/F 20/M Patient NO. 1 2 3 4 5 6 7 8 9 10 11 12 13 14 15 16 17 18 19 20 21 22 23 24 25 26 27 28 29 30 31 32 33 34 Hemorrhage Hemorrhage Hemorrhage Seizure Hemorrhage Hemorrhage Hemiparesis Seizure Headache Hemorrhage Hemorrhage Seizure Hemiparesis Headache Hemorrhage Headache Hemorrhage Seizure Hemorrhage Hemorrhage Seizure Seizure Headache Headache Seizure Seizure Seizure Seizure Seizure Seizure Hemorrhage Hemorrhage Headache Seizure Presentation Table 1 Summary of patients Deep Medial Deep Pure Medial Lateral Pure Medial Medial Pure Deep Lateral Lateral Lateral Deep Medial Pure Lateral Deep Lateral Lateral Medial Pure Medial Lateral Lateral Lateral Lateral Lateral Medial Lateral Medial Lateral Pure Sugita R L L R R R L R R R R L L L R R L L l L L L R L R L R R R L R L R R Side 2 2 2 2 2 2 2 1 2 2 1 1 2 2 2 2 2 2 2 1 2 2 1 3 2 2 2 2 2 2 3 2 2 2 Size 1 0 0 0 1 0 1 0 0 1 1 0 0 0 0 0 0 1 1 1 0 0 0 1 0 0 0 1 0 0 0 1 0 1 Drainage 1 1 1 0 1 1 0 0 0 0 1 1 1 1 1 0 0 0 1 1 0 1 1 1 0 0 0 0 0 1 0 1 0 0 Eloquence 4 3 3 2 3 3 3 1 2 3 3 2 3 2 3 2 1 3 3 3 2 3 2 5 2 2 1 2 2 4 3 3 2 3 Grade 3 2 0 1 4 0 1 1 1 1 3 1 0 1 1 1 4 1 3 3 1 1 1 1 1 1 0 1 1 1 1 0 1 0 Preoperative mRS 3 0 3 0 4 1 0 0 0 0 13 0 3 1 4 0 3 1 0 3 0 1 3 0 0 0 1 13 0 6 0 3 1 3 mRS(last follow-up) 16 32 14 26 15 33 15 29 12 34 15 32 26 32 18 31 15 11.5 29 15 12 28 26 35 32 32 6 35 9 14 18 20 30 9 Duration of follow-up (month) 1 1 1 0 1 0 0 0 0 1 1 0 1 0 1 0 1 0 1 1 0 0 1 0 0 0 0 1 0 1 0 1 0 1 Status of postop 1 0 1 0 1 0 0 0 0 0 1 0 1 0 1 0 1 0 0 1 0 0 1 0 0 0 0 1 0 Death 0 1 0 1 Status of follow-up Neurosurg Rev (2013) 36:541–549 543 infarction. The patient was included in the postoperative short-term evaluation and was excluded from the followup evaluation. Eighteen patients (43.9 %) had bad shortterm result and 23 (56.1 %) had good short-term result. Eleven patients (27.5 %) had bad long-term result and 29 (72.5 %) had good long-term result (Table 1). Illustrative case one History and examination This 34-year-old man with no significant medical history had suffered from medical intractable seizures for 1 year and was referred to our department. On admission the neurological examination disclosed nothing positive. The patient underwent angiography studies, which revealed an AVM bordering the right sylvian fissure (Fig. 1a, b). On orthotropic and lateral view, the right ICA angiogram showed a Spetzler–Martin grade II AVM (size, 2; deep venous drainage, 0; eloquence, 0) fed by a dilated middle cerebral artery. The nidus drained into the superior sagittal sinus. Operation and postoperative course A standard right pterional approach was performed and a large angioid lesion (Fig. 1c) was encountered. A complete removal was performed assisted by intraoperative real-time ultrasound. Postoperative course of the patient was uneventful and no neurological deficit occurred. Postoperative angiography was performed 1 week after operation (Fig. 1 d, e), and complete obliteration of the AVM was confirmed. At 1 year’s follow-up, he was seizure-free and had recovered well. Sugita Sugita Classification, L left, R right, mRS the modified Rankin Scale score Grade: refers to the Spetzler–Martin grading system, with points assigned according to arteriovenous malformation diameter or size, deep venous drainage, and eloquence. Status of postop.—1 means new neurological dysfunction or deterioration of original neurological deficit appeared shortly after operation, 0 means no neurological dysfunction and mitigation of original neurological deficit during 1 week after surgery 0 1 0 1 1 0 6 31 12 2 3 3 Lateral Lateral Lateral 15/M 17/F 8/M 39 40 41 Seizure Hemorrhage Hemorrhage R L L 2 2 2 0 1 0 0 0 1 1 1 0 1 4 0 0 0 0 0 29 8 8 24 3 1 2 2 Pure Medial Medial Medial 31/M 46/M 26/F 32/M 35 36 37 38 Seizure Hemorrhage Headache Seizure L R L L 2 1 2 2 1 0 0 0 0 0 1 1 1 1 1 1 0 1 1 1 Status of postop Duration of follow-up (month) mRS(last follow-up) Preoperative mRS Grade Eloquence Drainage Size Side Sugita Presentation Age (year) /sex Patient NO. Table 1 (continued) 0 0 0 0 Neurosurg Rev (2013) 36:541–549 Status of follow-up 544 Illustrative case two History and examination This 35-year-old man with no significant medical history had suffered from intermittent headache for 7 years and aggravated in the recent 3 years. On admission, the neurological examination disclosed nothing positive. The patient underwent angiography exam, which revealed a right pure sylvian fissure AVM (Fig. 2a, b). On orthotopic and lateral view, the right ICA angiogram showed a Spetzler–Martin grade II AVM (size, 1; deep venous drainage, 0; eloquence, 1) fed by a dilated middle cerebral artery. The nidus drained into the superior sagittal sinus and inferior petrosal sinus. Operation and postoperative course A standard right pterional approach was performed and a large angioid lesion was encountered. A complete removal was performed assisted by intraoperative real-time ultrasound. The patient had left hemiplegia after surgery and did not recover at discharge. Postoperative MRI was performed 1 week after operation (Fig. 2 c, d). At 2 years’ follow-up, he still had left Neurosurg Rev (2013) 36:541–549 545 Fig. 1 a, b The right ICA angiogram showed a Spetzler– Martin grade II AVM fed by a dilated middle cerebral artery. c Intraoperative screenshot obtained after opening the sylvian fissure through the right pterional approach showed the nidus was in the sylvian fissure. d, e Postoperative angiography confirmed complete obliteration of the AVM upper extremity hemiplegia and the mRS scores of followup were 3. Risk factors associated with short-term and long-term result in the univariate analysis Compared with the preoperative mRS score of the patients with and without previous bleeding by the rank-sum test, there was no statistically significant difference between the two groups (P value 0.09). The significance of each factor affecting the short-term and long-term result is shown in Table 2. Previous bleeding, eloquence of area involved, AVMs with deep venous drainage, age≤18, Sugita classification, and Spetzler–Martin grade classification were significant risk factors for short-term result by univariate analysis. Previous bleeding, eloquence of area involved, and Spetzler–Martin grade classification were significant risk factors for longterm result by univariate analysis. Multivariate logistic regression The multivariate logistic regression was on the base of results from the univariate analysis of risk factors associated with 546 Neurosurg Rev (2013) 36:541–549 Fig. 2 a, b The right ICA angiogram shows a Spetzler– Martin grade II AVM fed by a dilated middle cerebral artery. c, d Postoperative MRI with enhancement confirmed complete removal of the AVM and showed infarction on the right basal ganglia area short-term and long-term result. Seven factors, including age, sex, previous bleeding, deep venous drainage, eloquence of area involved, Sugita classification, and Spetzler–Martin classification, entered the mode of the parameter estimate associated with short-term result (Table 3). Previous bleeding (OR= 8.211, 95 % CI=1.760, 38.312) and deep venous drainage (OR=4.869, 95 % CI=0.991, 23.92) remained significant risk factors associated with short-term result. The incidence of postoperative transient neurological deterioration for patients with a ruptured AVM is as 8.211(95 % CI) times bigger as patients with an unruptured AVM. Patients with deep venous drainage were significantly more likely than those with superficial venous drainage to have postoperative transient neurological deterioration. Sex, previous bleeding, eloquence of area involved, and Spetzler–Martin classification entered the model of the parameter estimate associated with long-term result at the P< 0.1. Previous bleeding (OR = 7.000, 95 % CI = 1.476, 33.207) remained significant risk factors associated with the long-term result in the multiple regression model (Table 4), which manifested that the incidence of bad long-term result for patients with a ruptured AVM is 7 (95 % CI) times bigger as compared to patients with an unruptured AVM. Discussion Based on our results, despite different Sugita classification subtypes, sylvian fissure AVMs patients’ prognosis with microsurgical resection are better than expected; a history of AVM bleeding is a risk factor for postoperative temporary neurological deterioration and for longterm adverse outcome, while the AVM deep venous drainage is a risk factor only for temporary neurological deterioration. Previous hemorrhage in common intracerebral AVMs perhaps helps neurosurgeons to dissect the margin between the nidus and surrounding parenchyma [6]. However, sylvian fissure AVM which locates in or adjacent to the sylvian fissure involves the middle cerebral artery and is surrounded by critical structures such as the basal ganglia and internal capsule. A prior bleeding from AVM frequently cause hematoma or subarachnoid hemorrhage (SAH) in sylvian fissure [10], which later always lead to adhesion and blurred boundary between the nidus and middle cerebral artery or these surrounding critical structures. These will bring extra difficulty of visualization and dissection of the AVM planes. Obscure anatomy might cause unexpected injury to critical structure and accidental intraoperative Neurosurg Rev (2013) 36:541–549 547 Table 2 Risk factors associated with short-term and long-term results (chi-square test) Risk factors Short-term result Long-term mRS Bad (No., %) Good (No., %) 8 (80.0) 10 (32.3) 2 (20.0) 21 (67.7) 8 (32.0) 17 (68.0) Female 10 (62.5) Previous bleeding Yes 12 (75.0) No 6 (24.0) Drainage Deep 10 (71.4) Superficial 8 (29.6) Eloquence Yes 12 (60.0) No 6 (28.6) Sugitaa 6 (37.5) Agea ≤18 >18 Sex Male Pure Lateral Medial Deep Diameter 0–3 cm 3–6 cm P 0–2 (No., %) 0.012 3.685 0.055 3–6 (No., %) χ2 P 6 (60.0) 23 (76.7) 4 (40.0) 7 (23.3) 0.418 3.532 0.080 20 (83.3) 4 (16.7) 9 (56.3) 7 (43.8) 4 (25.0) 19 (76.0) 10.303 0.001 8 (50) 21 (87.5) 8 (50) 3 (12.5) 6.771 0.009 4 (28.6) 19 (70.4) 6.540 0.011 8 (61.5) 21 (77.8) 5 (38.5) 6 (22.2) 1.161 0.281 8 (40.0) 15 (71.4) 4.108 0.043 11 (57.9) 18 (85.7) 8 (42.1) 3 (14) 3.872 0.049 4 (57.1) 14 (82.4) 9 (81.8) 2 (20) 3 (42.9) 3 (17.6) 2 (18.2) 3 (60) 0.188 4 23 2 9 21.67 20.63 0.655 2 0 15.00 4 (57.1) 5 (29.4) 4 (33.3) 5 (100.0) 3 (42.9) 12 (70.6) 8 (66.7) 0 (0) 3 15 3 18 22.25 21.32 2 12.00 15 7 1 16.32 24.95 25.67 0.008 17 11 1 2 8 1 17.11 23.42 25.00 0.024 2 8 9 4 18.83 21.57 19.32 23.39 0.709 3 10 10 6 0 4 4 3 15.00 20.71 20.71 21.67 0.717 6–cm 0 Spetzler–Martin I,II 4 III 12 IV,V 2 Bleeding in surgery (ml) 0–100 1 100–500 7 500–1,000 5 1,000õ 5 a χ2 0.031 0.391 Fisher’s test AVM rupture. In addition, hematoma and SAH would compress the surrounding important structures or cause following possible cerebral vasospasm, both possibly leading to long-term neurological deficit [11]. These might explain why a bleeding history was a risk factor for short-term and long-term adverse prognosis for sylvian fissure AVMs. Deep venous drainage is another risk prognosis factor for sylvian fissure AVM in the short term. Sylvian fissure AVMs with deep venous drainage are always located in the deep brain and often share blood drainage with basal Table 3 parameter estimate associated with short-term result Parameter estimate S.E. Bleedinga 2.105 Drainageb 1.583 Constant −1.640 P OR 95 % CI 0.786 0.007 8.211 1.760,38.312 0.812 0.051 4.869 0.991,23.922 0.578 0.005 0.194 a Without a history of symptomatic AVMs bleeding=0; with a history of symptomatic AVMs bleeding=1 b Superficial venous drainage=0; deep venous drainage=1 548 Neurosurg Rev (2013) 36:541–549 Table 4 Parameter estimate associated with long-term result Parameter estimate S.E. Bleedinga 1.946 Constant −1.946 P OR 95 % CI 0.794 0.014 7.000 1.476, 33.207 0.617 0.002 0.143 a Without a history of symptomatic AVMs bleeding=0; with a history of symptomatic AVMs bleeding=1 ganglia and thalamus. Deep location of the AVM nidus [8] and the presence of deep venous drainage [3] have been regarded as risk factors for hemorrhage from an AVM. Additionally, shortly after nidus was surgically removed, vein drainage from surrounding structure might be also affected causing transient neurological deficits. As time passed by, the venous drainage might redistribute. This might explain why the deep venous drainage had significant effect on the short-term outcome. Interestingly, some factors such as eloquent area involved, Spetzler–Martin grade classification, and Sugita classification show significant (P<0.05) in the univariate analysis; however, these factors did not present statistic significance (P<0.05) in the multivariate logistic regression model finally. The model always allows the most significant factor to enter preferentially. Considering the interaction among all factors, the three factors might not be powerful enough to influence the prognosis and just manifest certain tendency between this single factor and the unfavorable prognosis. Their more detailed effects on the prognosis need to be explored in a larger population. Bleeding is more likely to occur to AVM patients with a history of bleeding or deep venous drainage [9], which may support choosing more invasive treatment for this kind of patients. However, from our results, sylvian fissure AVM patients with a prior bleeding or deep venous drainage might have bad long-term or short-term outcomes if they select microsurgery. It seems to be a dilemma. In this situation, decision-making for surgery should be much more cautious. Limitation Indeed, previous AVM bleeding may cause preoperative neurological deficits and will affect the long-term prognosis. We compared the preoperative mRS score of the patients with and without previous bleeding; we found that there was no statistically significant difference between the two groups. However, the P value was 0.09, which is approaching the P value 0.05. It is also possible that the significant difference of preoperative status of patients between two groups might exist, which need a larger population to prove. At the same time, we realized that previous bleeding might not only affect preoperative patient’s status but also increase surgical difficulties in the operation. Both might be as a whole leading to their bad short- or long-term surgical results. Additionally, some factors such as arterial injury, venous infarction, vasospasm, etc., might play a very important role and affect the postoperative outcome; these factors will be evaluated in a future prospective study. Statistical analysis only provide mathematical logic, which cannot clarify the underlying reasons that a history of AVM bleeding and AVM deep venous drainage is superior to other factors to affect the prognosis. Meanwhile, a larger numbers of sylvian fissure AVM patients treated with microsurgery with long-term outcomes are required for better prognosis evaluation in the future. Conclusion Despite different Sugita classification subtypes, sylvian fissure AVMs’ results with microsurgical resection are better than expected; a history of AVM bleeding is a risk factor for postoperative temporary neurological deterioration and for longterm adverse outcome, while the AVM deep venous drainage is a risk factor only for temporary neurological deterioration. Acknowledgments We are greatly indebted to Dr. Yang Wang for their precious statistic assistance. Funding This study is supported by a grant “National Science and Technology Support Program (No: 2011BAI08B08)” (Principal Investigators, Professor Shuo Wang) from the Ministry of Health, China. References 1. ApSimon HT, Reef H, Phadke RV, Popovic EA (2002) A population-based study of brain arteriovenous malformation:longtreatment outcomes. Stroke 33(12):2794–800 2. Brown RD Jr, Wiebers DO, Torner JC, O’Fallon WM (1996) Incidence and prevalence of intracranial vascular malformations in Olmsted County, Minnesota, 1965 to 1992. Neurology 46(4):949–5 3. Duong DH, Young WL, Vang MC, Sciacca RR, Mast H, Koennecke HC, Hartmann A, Joshi S, Mohr JP, Pile-Spellman J (1998) Feeding artery pressure and venous drainage pattern are primary determinants of hemorrhage from cerebral arteriovenous malformations. Stroke 29:1167–1176 4. Hillman J (2001) Population-based analysis of arteriovenous malformation treatment. J Neurosurg 95(4):633–7 5. Laakso A, Hernesniemi J (2012) Arteriovenous malformations:epidemiology and clinical presentation. Neurosurg Clin N Am 23:1–6 6. Lawton MT, Du R, Tran MN, Achrol AS, McCulloch CE, Johnston SC, Quinnine NJ, Young WL (2005) Effect of presenting hemorrhage on outcome after microsurgical resection of brain.arteriovenous malformations. Neurosurgery 56(3):485–9 7. Lawton MT, Lu DC, Young WL (2007) Sylvian fissure arteriovenous malformations:an application of the Sugita classification to 28 surgical patients. Neurosurgery 61(1):29–36 8. Mast H, Young WL, Koennecke HC, Sclacca RR, Osipov A, Pile-Spellman J, Hacein-Bey L, Duong H, Stein BM, Mohr JP Neurosurg Rev (2013) 36:541–549 (1997) Risk of spontaneous haemorrhage after diagnosis of cerebral arteriovenous malformation. Lancet 350:1065–1068 9. Pollock BE, Flickinger JC, Lunsford LD, Bissonette DJ, Kondziolka D (1996) Factors that predict the bleeding risk of cerebral arteriovenous malformations. Stroke 27(1):1–6 10. Qureshi AI, Mendelow AD, Hanley DF (2009) Intracerebral haemorrhage. Lancet 373:1632–1644 11. Schmieder K, Moller F, Engelhardt M, Scholz M, Schregel W, Christmann A, Harders A (2006) Dynamic cerebral autoregulation in patients with ruptured and unruptured aneurysms after induction of general anesthesia. Zentralbl Neurochir 67:81–87 12. Stapf C, Mast H, Sciacca RR, Berenstein A, Nelson PK, Gobin YP, Pile-Spellman J, Mohr JP; New York Islands AVM Study Collaborators (2003) The New York Island’s AVM study: design, study progress, and initial results. Stroke 34(5):e29–33 13. Sugita K, Takemae T, Kobayashi S (1987) Sylvian fissure arterivenous malformations. Neurosurgery 21:7–14 14. van Swieten JC, Koudstaal PJ, Visser MC, Schouten HJ, van Gijn J (1998) Interobserver agreement for the assessment of handicap in stroke patients. Stroke 19(5):604–7 15. Wang S, Zhao HY, Zhao YL (2011) Microsurgical treatment for sylvian fissure arteriovenous malformations. Zhonghua Yi Xue Za Zhi 91:1609–12 16. Zimmerman G, Lewis A, John M, Tew JM Jr (2000) Pure sylvian fissure arteriovenous malformations. J Neurosurg 92:39–44 Comments Feres Chaddad, Jose Maria Campos Filho, Evandro de Oliveira, São Paulo, Brazil The authors provide an impressive series of sylvian fissure AVMs in a short space of time, which constitute a challenging subgroup of lesions. The Spetzler–Martin grade has provided the orientation about the surgical risk of AVMs. Its size, distribution along the sylvian fissure and the relation between the nidus and the middle cerebral artery clearly define the surgical morbidity. The correlation of AVM with the insula lobe, the frontal, parietal and temporal cortex influences the choice in treatment and patients´ outcome. Moreover, the AVMs supplied by the lateral lenticulostriate arteries show higher morbidity than others because such arteries are related to the central core blood supply. The deep venous drainage is a clear risk to neurological deterioration because the former indicates the impairment of the insula’s lobe drainage veins. The surgical management of AVMs demands the integrated approach to a specially trained neurosurgeon, an interventional neuroradiologist and a radiosurgeon working as a team. Each AVM is studied in order to achieve the best treatment. Thus, they can be surgically treated, a small number can be treated with radiosurgery and a combination of embolization can be used for some of them before surgery. Hideyuki Yoshioka, Hiroyuki Kinouchi, Yamanashi, Japan Arteriovenous malformations (AVMs) localized in the sylvian fissure constitute a challenging subgroup of lesions to manage surgically. In this article, Liu et al. reported their surgical experience of 41 patients with sylvian fissure AVM, which is one of the biggest series of this rare entity of AVM so far, and presented the excellent surgical outcome. Complete removal of AVM was achieved in all but one case, and 72.5 % of the patients showed good long-term outcome. The authors retrospectively analyzed their short-term and long-term surgical outcomes. In the multivariate logistic regression analysis, previous bleeding and deep venous drainage were associated with temporary neurological deterioration. For long-term outcome, previous bleeding was related to poor outcome. It is of interest that eloquency of 549 the lesion, Spetzler–Martin grade, and Sugita classification were not a significant risk factor in their analysis. Although this article provided practically important information, there are some limitations in the study. As the authors pointed out, the factors regarding bleed or deep venous drainage affecting the postoperative poor outcome were not clarified. Brain parenchymal injury, intraoperative AVM rupture, arterial injury, venous infarction, and cerebral vasospasm were considered to worsen neurological symptoms after AVM surgery1. Information about such factors in this large series of sylvian fissure AVM are valuable for the neurosurgical community, and such profound analyses would be encouraged in future. References 1. Pik JH, Morgan MK (2000) Microsurgery for small arteriovenous malformations of the brain: results in 110 consecutive patients. Neurosurgery 47:571–575 Thomas Kretschmer, Oldenburg, Germany Sylvian fissure AVMs are a rare type (around 10 % of AVMs), whose microsurgical removal demands vascular expertise. They have been dealt with in the literature before (E.G. Lawton, Lu, Young, University of California, San Francisco Brain Arteriovenous Malformation Study Project, 2007). Additional information with regard to evaluation and risk assessment of natural history and surgical risk assessment and outcome analysis is very useful and welcome. The presented series of 355 AVM overall is rather large and has been operated on within a remarkable short time intervall of only 2.5 years by a single neurosurgeon. The findings of this series with regard to short- and long-term outcome therefore are precious. Statistical analysis underlines the higher incidence of neurological deficits as compared to AVM treatment in other locations; however, it also confirms that prognosis after surgery also was better than expected. Important results to me were: one third had an unfavorable outcome. The incidence of postoperative transient neurological deterioration with a ruptured sylvian fissure AVM was 8 times higher as compared to unruptured ones. Ruptured AVMs had a 7 times larger chance for a bad long-term result. The mentioned other sylvian fissure series demonstrated slightly different outcome results (Lawton et al. 2007). I congratulate the authors for this remarkable series and report thereof. Yasser Orz, Alexandria, Egypt The arteriovenous malformations (AVM) localized in the sylvian fissure constitute a challenging subgroup of lesions. The authors reported their experience with 41 patients harboring such lesions according to Sugita’s Classification, out of 355 patients with AVM treated with microsurgical resection at their institute between June2009–Dec. 2011. They analyzed their results stressing on risk factors responsible for short-term and long-term bad outcome according to mRS. In the univariate analysis, previous bleeding, eloquence of area involved, and Spetzler–Martin grade were significant risk factors for long-term bad outcome; but in multivariate logistic analysis, only the previous bleeding was a risk factor for long-term bad outcome. Sugita’s classification, deep venous drainage, and age are risk factors for transient short-term bad outcome. Although they showed excellent results with microsurgical resection where complete removals of AVM were achieved in all patients except one and only one patient died, a number of points already mentioned by the authors deserve reemphasis. The Sugita’s classification does not guide the surgical approach, predict long-term surgical outcome, or affect the clinical decision process. Adjuvant treatment modalities (embolization, radiosurgery) may be very useful for targeting deep feeders or deep portions of AVMs thereby increasing the safety of surgical resection. The authors should be congratulated for such good surgical results and thoughtful analysis of their work.