Acta Neurochir (2003) 145: 273–282 DOI 10.1007/s00701-003-0003-8 Acta Neurochirurgica Printed in Austria Clinical Article Large sphenocavernous meningiomas: Is there still a role for the intradural approach via the pterional-transsylvian route?* F. Tomasello, O. de Divitiis, F. F. Angileri, F. M. Salpietro, and D. d’Avella Neurosurgical Clinic, Department of Neurosciences, Psychiatric and Anesthesiological Sciences University of Messina, Messina, Italy Published online April 28, 2003 6 Springer-Verlag 2003 Summary Introduction Background. Large-sized sphenocavernous meningiomas represent a surgical challenge. Although the role of skull base techniques with combined extra- and intradural steps has been recently emphasized, pure intradural resection tactics via the pterional route constitute the traditional microsurgical approach for resection of such tumours. Method. We report the application of the pterional-transsylvian approach in 13 patients with sphenocavernous meningiomas. This series is unique because it includes only patients with tumours exceeding 5 cm in their greatest dimension. Findings. A gross total resection was accomplished in 10 patients (77%). Eight patients had a good outcome, one had a persistent mild hemiparesis, and one died. No recurrences occurred in this group. Three patients (23%) had subtotal resections owing to invasion of the cavernous sinus in one instance and encasement of the middle cerebral artery in the others. Two had a good outcome and one died. In these patients minimal asymptomatic tumour progression was seen 3 and 6 years after surgery. The overall surgical outcome was good in 10 patients (77%), fair in one, and death in two. Interpretation. In our experience, large sphenocavernous meningiomas may be operated on adopting pure intradural resection tactics via the pterional-transsylvian route with rates of gross total removal and surgical complications related to brain retraction or vascular manipulation comparable to those of extensive skull base approaches. The traditional intradural pterional transsylvian approach continues to have a place in the treatment of these lesions. Sphenocavernous meningiomas, arising from the dura covering the medial portion of the sphenoid bone, occupy the region of the anterior clinoid and adjacent medial sphenoid wing and involve the pericavernous or cavernous sinus structures [16, 24]. These tumours are di¤erentiated from clinoidal meningiomas on the basis of their dural attachment, growth pattern, neurovascular relationships and clinical presentation. Tumours with an ‘‘en masse’’ [3, 4] growth pattern may attain surprisingly large size with relatively minimal symptoms. Such huge (b5 cm in diameter) meningiomas still represent a surgical challenge. Recent reports have emphasized the role of contemporary skull base surgical techniques with combined extra- and intradural steps for resection of large sphenocavernous meningiomas [2, 9]. Nevertheless, the ‘‘pure’’ intradural resection tactics via the pterional route, that are the traditional microsurgical approach to these lesions, can result in excellent outcomes after operation [3, 4, 5, 10, 16, 24]. Very large tumours, however, were not specifically considered in these publications. This paper describes the application of the pterional transsylvian approach in 13 patients who had a sphenocavernous meningioma, larger than 5 cm in the greatest dimension. The aims of this article are: 1) to consider specifically the issue of suitability of the intradural pterional-transsylvian route for large-sized sphenocavernous meningiomas; and 2) to investigate if this approach contributes to minimizing morbidity after operation. Keywords: Surgical approach; meningioma; skull base surgery; cavernous sinus. * This paper was supported in part by Grant ‘‘Piano B008 – P.R. 2’’ from M.U.R.S.T. and European Community. 274 F. Tomasello et al. Fig. 1. Case 2: preoperative magnetic resonance images with contrast enhancement: (A) coronal and (B) axial planes showing a large sphenocavernous meningioma in a 63 years old woman who presented with headache and short-term memory impairment Patients and methods Clinical presentation Thirteen patients harbouring a large-sized sphenocavernous meningioma were operated on by the senior author (F.T.) between June 1988 and June 2000 at the Neurosurgical Clinic of the University of Messina School of Medicine in Messina, Italy. They were 11 women and 2 men with a mean age of 57.6 years (range 43 to 71 years). The clinical records, neuroradiological examinations, and operative notes and videotape recordings of the procedures of these patients were examined retrospectively. Signs on presentation consisted of chronic headache present in eight of thirteen patients (61.5%), seizures in eight (61.5%), visual acuity or visual field impairment in three (23%), and altered mental status and personality changes in four (30.7%) (Table 1). The beginning of symptoms preceded diagnosis by 3 to 36 months (average 14.6 months). No patient was admitted in comatose condition requiring emergency craniotomy. Fourteen operations were performed in thirteen patients. Karnofsky performance status was taken as a gross measure of neurological functional impairment [13]. When graded preoperatively, Karnofsky index averaged 70% (range 60 to 90%). Post-operative clinical and neuroradiological follow-up periods ranged from 12 to 156 months (average 48.3 months). Preoperative neuroradiological findings All but one patient (in whom a contrast-enhanced CT scan was obtained) underwent sequential contrast-enhanced magnetic resonance imaging (including T1 weighted, T2 weighted, spin-echo and gradient echo multiplanar images), preoperatively, in the early postoperative period, and at subsequent follow-up examinations (6–12 months postoperatively and when this series was reviewed for publication purposes). Preoperative MR images were evaluated for tumour size, direction of growth in anterior and middle cranial fossa, cavernous sinus involvement, involvement of the carotid, anterior and middle cerebral arteries as well as the optic apparatus, and degree of perilesional oedema. The tumour’s maximum diameter was measured and found to be greater than 5 cm in all cases (mean 5.7 cm). The largest tumour of this series reached 7 cm in maximum diameter (Fig. 1). The cavernous sinus structures were clearly invaded in one case while in the others the tumour appeared to be only adherent to the sinus lateral wall. The tumour never extended into the sella turcica. The carotid artery, the carotid bifurcation and the A1 and M1 segments were engulfed by the tumour in all patients as confirmed by cerebral DSA which was obtained in all cases. Tumour embolization was performed only in one patient in whom the external carotid artery contribution to meningioma vascularization appeared particularly dominant. The extent of perilesional oedema was graded as severe in ten cases (83%) (Fig. 2) and moderate in three cases. In all cases it was of the di¤use type [19]. Postoperative magnetic resonance evaluation The post-operative early-phase MR images were examined for extent of tumour removal, postoperative sequelae, and the presence of additional oedema or vascular congestion. Standard late followup MRI served to confirm completeness of excision and lack of recurrence. Studies were supplemented by obtaining fluid attenuated inversion recovery (FLAIR) sequences to evaluate postoperative changes in the brain parenchyma. FLAIR sequences were performed according to the scanning parameters reported by Tsuchiya et al. [22] and other reports from our group [6]. Parameters examined included evidence of permanent parenchymal alterations, including degenerative changes or tissue gliosis, and persistence of areas of white matter oedema. These changes were examined in regions of interest of the frontal and temporal lobes ipsilateral to the operative approach. Operative technique The patient is placed supine with shoulder ipsilateral to the approach slightly elevated and the head fixed in the Mayfield head- Large sphenocavernous meningiomas: Is there still a role for the intradural approach via the pterional-transsylvian route? 275 Fig. 2. Case 7: (A) pre-operative axial T2 weighted magnetic resonance images showing severe peritumoural edema (di¤use type). (B) Postoperative scan at six months follow-up demonstrating complete resolution of the oedema rest and turned 45 to the opposite side. The skin incision, the temporalis muscle preparation, and the bony steps are performed as for a standard pterional craniotomy, including extensive drilling of the sphenoid wing and temporobasal craniectomy. In this step, care must be taken to identify and coagulate the deep branches of the middle meningeal artery (e.g. orbito-meningeal artery and its branches) allowing partial devascularization of the tumour. After opening the dura the sylvian fissure is dissected and widely opened. This allows elevation of the basal posterior aspect of the frontal lobe with minimal retraction pressure, also as a consequence of the upward dislocation of the frontal lobe exerted by the tumour itself. The capsule is coagulated and incised and the tumour partially debulked with the aid of the ultrasonic aspirator. Central tumour enucleation is alternated to coagulation of the feeding vessels at the base of the tumour along the sphenoid ridge, as well as control and coagulation of leptomeningeal feeding arteries. Tumour devascularization results in reduction in turgor and consistency and facilitates its debulking. Because these large tumours grow massively into the sylvian fissure, dissection commences at a more distal point. The branches of the sylvian artery are identified and the artery is followed proximally to establish a dissection plane. This manoeuvre allows a better spatial identification of the seeming ‘‘intratumoural’’ position of the encased vessels. The tumour is removed in a piecemeal fashion under strict visual control of the middle cerebral artery and its branches, which can be shifted, stretched, or encased. In the latter case the tumour may remain separated from the arteries by an arachnoid layer, which facilitates dissection, conducted either with sharp instruments or blunt dissection. During this phase small arterial branches from the internal carotid artery nourishing the tumour are coagulated and divided. When enough tumour volume reduction has been achieved, the proximal (paraclinoid segment) carotid artery, the optic nerve, and the cisternal portion of the III cranial nerve are recognized and dissected free from the tumour. After control of the paraclinoid ICA is gained, dissection of the MCA and its perforating branches, and the posterior communicating and anterior choroidal arteries can be completed. The base of the tumour can now be fully exposed and devascularization completed. The invaded dura is coagulated and resected. The dissection is finally carried out on the lateral wall of the cavernous sinus, peeling the walls with sharp instruments and completing tumour removal with cautious bipolar coagulation. In only one case the lateral wall barrier was frankly crossed by the tumour. In such instances we intentionally follow a predetermined strategy aimed at removing the extracavernous portion of the tumour and preserving anatomic continuity and existing function of cavernous sinus vascular and nervous structures [15]. Results Clinical features and outcome The salient aspects of each patient’s peri- and postoperative course are summarized in Table 1. A gross total resection (defined as grade II according to De Monte tumour removal grading system) [8] (Table 2) was accomplished in 10 patients (77%) who underwent eleven operations. In all cases the surgeon’s impression was confirmed by postoperative MR studies. Eight patients had a good outcome, 1 patient had a mild persistent left hemiparesis and 1 patient died from pulmonary embolism after she had recovered from anaesthesia and appeared neurologically intact. No recurrence was identified at late clinical and neuroradiological follow-up examinations in this group of patients. Three patients (23%) had subtotal resections 276 F. Tomasello et al. Table 1. Summary of thirteen patients with sphenocavernous meningiomas Case n , age, sex Symptoms on admission Max dimension (cm) Surgical approach Extent of resection (De Monte Grade) Outcome Follow-up (months) Case 1 58/F Case 2 63/F Case 3 62/M Case 4 45/F Case 5 66/M Case 6 69/F Case 7 46/F Case 8 43/F Case 9 52/F Case 10 67/F Case 11 71/F Case 12 54/F Case 13 58/F headache, visual deficit, seizures headache, short term memory impairment headache, seizures intracranial hypertension headache, frontal syndrome, seizures headache, visual deficit frontal syndrome headache, seizure seizure seizure headache, visual deficit seizure, frontal syndrome headache, seizure 5.3 7 5.4 5 6 6 5 5.2 6.6 5 6 6 6.5 left pterional left pterional right pterional right pterional left pterional left pterional left pterional right pterional left pterional left pterional left pterional left pterional left pterional IVa, II1 II II IVa IVa II II II IVa II II II II Good Died2 Good Fair Good Good Good Good Died3 Good Good Good Good 156 (*) N/A 96 88 53 39 21 21 N/A 18 15 12 12 1 Recurrence 3 years later, 2nd operation, total resection with a good outcome. 2 Pulmonary embolism 2 days after surgery. 3 Surgical complication (*) Time length from the second operation in 1991. Good: return to previous occupation; Fair: no major neurological deficit, but not able to return to previous occupation. Table 2. De Monte tumour removal grading system [8] Grade Definition I complete microscopic removal of tumour and dural attachment with any abnormal bone complete microscopic removal of tumour with diathermy coagulation of its dural attachment complete microscopic removal of intra- and extradural tumour without resection or coagulation of its dural attachment complete microscopic removal of intradural tumour without resection or coagulation of its dural attachment or of any extradural extension intentional subtotal removal to preserve cranial nerves or blood vessels with complete microscopic removal of attachment partial removal leaving tumour < 10% in volume partial removal leaving tumour > 10% in volume, or decompression with or without biopsy II IIIa IIIb IVa IVb V (defined as grade IVa in De Monte grading system) owing to invasion of the cavernous sinus in one instance and encasement with frank tumoural infiltration of the MCA trunk in the others. Of these patients, one died from a surgical complication and 2 had a good outcome. In these patients, minimal asymptomatic tumour progression was seen 3 and 6 years after surgery, respectively (Figs. 3, 4). No patient received post-operative radiotherapy. Karnofsky performance status graded 6 months postoperatively averaged 90% (range 70 to 100%). The overall surgical outcome was good in 10 patients (77%) who had resumed independent activity by 3 months after surgery, fair in one patient, and death in two. Seven patients (53.8%) required blood replacement in the perioperative time. The mean amount of blood replaced was 208 cc. There were no permanent cranial nerve deficits; however, three patients experienced a transient III nerve palsy that had recovered completely three months after surgery. Magnetic resonance imaging investigations In the total removal group, early post-operative studies revealed no evidence of a surgical complication and confirmed completeness of excision (Figs. 5, 6). Lack of recurrence was documented by late follow-up contrast-enhanced MR scans, also demonstrating no evidence of any significant structural change and the resolution of the intense perilesional oedema demonstrated in preoperative studies. Late post-operative changes in the frontal and temporal lobes ipsilateral to the approach were specifically examined on FLAIR MR sequences (Fig. 7). These lobes consistently exhibited a repetitive pattern of post-operative alterations, which were thought to represent permanent parenchymal gliosis. It should be noted, however, that the extent of such structural alterations was limited and that they did not result in specific functional morbidity in the present series. Large sphenocavernous meningiomas: Is there still a role for the intradural approach via the pterional-transsylvian route? 277 Fig. 3. Case 4: (A) pre-operative contrast-enhanced CT scan of a large sphenocavernous meningioma. (B and C) Contrast-enhanced follow-up CT scans obtained at 4 and 6 years post-operative respectively. Note the minimal progression of the residual tumour embedding the MCA trunk. Due to the asymptomatic course this patient was treated conservatively Fig. 4. Case 5: Coronal T1 weighted contrast-enhanced magnetic resonance images showing: (A) pre-operative appearance of a large sphenocavernous meningioma; (B) its follow-up enhanced MRI scan at 6 months and (C) 3 years follow-up. Note the minimal progression of the residual tumour into the cavernous sinus. Due to the asymptomatic course this patient was treated conservatively Discussion In this era of microneurosurgical technique refinements, excellent surgical results can be achieved in excising skull base meningiomas. However, meningiomas arising from the medial sphenoid ridge with involvement of the lateral wall of the cavernous sinus or invasion of the sinus itself, and achieving very large size, still represent a surgical challenge. According to Yaşargil [24] sphenocavernous meningiomas are a distinct subgroup of medial sphenoid meningiomas. Day [9] defined sphenocavernous meningiomas as those arising from the dura covering the sphenoid ridge, with or without invasion of the peri cavernous and cavernous sinus structures. This classification is important from the nosographic point of view, and has clinical implications. Sphenocavernous meningiomas are distinguished from medial sphenoidal meningiomas originating from the superior and/or lateral aspect of the anterior clinoid process [2]. Due to their growth pattern, clinoidal meningiomas are characterized by an earlier involvement of the optic nerve 278 F. Tomasello et al. Fig. 5. Case 7: (A) pre-operative coronal T1 weighted magnetic resonance images with contrast enhancement showing a large sphenocavernous meningioma (max diameter 5 cm). (B) Post-operative scan at six months follow-up demonstrating complete excision of the lesion (De Monte grade II) and proximal carotid artery. In contrast sphenocavernous meningiomas tend to spread lateral-inferiorly into the middle cranial fossa so that ICA and optic and oculomotor nerves are generally involved later. This di¤erence may explain the huge dimensions they may attain before becoming symptomatic. For example, while visual disturbances were present in 84% of cases of clinoidal meningiomas reported by A1-Mefty [2], only 3 of our 13 patients (23%) had visual impairment. The foregoing anatomical, radiological and clinical considerations, lead us to suggest the use of the term sphenocavernous meningiomas should be reserved for this particular subgroup of lesions. Literature review The pterional approach followed by intradural debulking and microsurgical resection of the tumour is the most widely used surgical route for large-sized meningiomas of the middle cranial base. The standard pterional intradural approach for the removal of such tumours has been comprehensively described by Dolenc [10], Bonnal [3], Ojemann [16], and systematically adopted by Yaşargil [24]. The advantages and disadvantages of this surgical strategy have been recently discussed and compared with those o¤ered by contemporary cranial base surgical techniques in a paper reporting six patients with large sphenocavernous meningiomas [9]. The present report presents our experience using the pterional-transsylvian route followed by intradural microsurgical tumour resection in a selected series of thirteen patients with a large sphenocavernous meningioma. To our knowledge, this series is the largest in the literature that specifically includes only patients with a sphenocavernous meningioma larger than 5 cm diameter. A gross total removal was achieved in 77% of patients and 77% resumed an independent life, with marked improvement in their neurological symptoms. It is well known that the likelihood of unsatisfactory surgical results and of failure to achieve complete removal increases when a tumour is larger than 3 cm [1, 21]. When compared to the results in published series of Sphenocavernous meningiomas, the results from the present series support the suitability of the intradural approach, via the pterional-transsylvian route, for resection of such large-sized meningiomas (Table 3). In 1979 Dolenc reported on 10 patients who had been operated upon via a bifrontal approach (in 2 cases) or a pterional approach (8 cases). Two deaths occurred, 2 patients developed a transient IIIrd nerve paresis, and four patients experienced a transient hemiparesis. Nevertheless, the final outcomes were good for these 8 patients [10]. In 1991 Bonnal presented 15 patients with an en masse sphenocavernous meningioma; eight of these patients had slight or Large sphenocavernous meningiomas: Is there still a role for the intradural approach via the pterional-transsylvian route? 279 Fig. 6. Case 11: (A) pre-operative coronal T1 weighted magnetic resonance images with contrast enhancement showing a large sphenocavernous meningioma (max diameter 6 cm). (B) Post-operative scan at six months follow-up demonstrating complete excision of the lesion (De Monte grade II). (C and D) Late post-operative FLAIR MR axial views. There is no evidence of permanent structural changes. The frontal and temporal lobes exhibit circumscribed areas of hyperintense signal changes. These alterations may represent permanent parenchymal gliosis severe post-operative morbidity. The other seven patients had good outcomes [3]. In 1992 Ojemann reported 17 patients, some of whom had a clinoidal meningioma, operated upon via a fronto-temporal craniotomy. A subtotal removal was achieved in 14 patients and a radical subtotal removal in the remaining three. The outcome was good in 16 patients. One patient had a permanent dysphasia and hemiparesis [16]. In his monograph (1996) Yaşargil described 9 patients with ‘‘medial sphenoid’’ meningiomas operated upon via a pterional approach. Seven patients experienced a good outcome and the other two had a ‘‘fair’’ outcome [24]. Contemporary cranial base surgical techniques do have a major role in the treatment of such tumours, particularly when a large sphenocavernous meningioma has extensively crossed the wall of the cavernous sinus [11, 14, 18]. Very recently, Day [9] reported six patients in whom an aggressive skull 280 F. Tomasello et al. Table 3. Summary of selected published series of sphenocavernous meningiomas Author, year N of patients Approach Cook, 1968 (5) Dolenc, 1979 (10) Bonnal, 1980 (3) Ojemann, 1992 (16) Yasargil, 1996 (24) Day, 2000 (9) Present series, 2001 11 10 7 17 9 6 13 pterional, intradural bifrontal, pterional pterional intra-extradural pterional intradural pterional intradural extensive extradural pterional intradural Excision Follow-up 7 subtotal 3 RST, 14 ST 1–13 years 5 (1–11) years 2 ST, 4 T 3 ST, 10 T 24 months (max) 48.3 (12–156) months Outcome 2 D, 4 SD 2D 3 D, 1 SD, 3 GO 1 SD, 16 GO 2 MD, 7 GO 6 GO 10 GO, 1 MD, 2 D RST Radical subtotal resection; ST subtotal resection; T total resection; D Death; SD severe disability; MD Moderate disability; GO good outcome. base surgical strategy was adopted to resect a large sphenocavernous meningioma. Extensive bone work at the cranial base was performed in each patient. Unroofing of the foramina rotundum, ovale, and spinosum of the superior orbital fissure, and of the optic canal, removal of the anterior clinoid process, and elevation of the undersurface of the temporal lobe, were performed before opening the dura. Following this strategy, four patients had a gross total resection, and two had only a subtotal resection as result of invasion of the cavernous sinus or the middle cerebral artery. Two patients experienced a transient III nerve paresis, and two developed transient postoperative cerebral oedema that required intensive treatment. All six patients, however, had a good outcome. The use of this technique resulted in low blood loss during the operation and obviated the need for preoperative embolization [9]. Technical considerations The principal advantages claimed for aggressive skull base approaches to these lesions include: 1) better control of arterial blood supply to the tumour 2) wider exposure and minimization of brain retraction 3) control of neurovascular structures at the cranial base 4) more possibility of complete excision and hence long term, recurrence-free tumour control. These issues deserve detailed discussion. 1) Interruption of its blood supply before a debulking tumour is undoubtedly a great advantage. In our experience, however, pure intradural resection tactics did not result in significant intraoperative blood losses as judged from blood replacement needs. In this context we emphasize that a component of the vascularization of these meningiomas is from the ICA dural and leptomeningeal branches [23], which can be dissected and controlled during the intradural phase of the operation. 2) According to Yaşargil [24], the pterionaltranssylvian approach takes advantage of those planes and spaces naturally provided to expose the base of the brain without significant brain retraction. Moreover, large tumours produce large ‘‘birth’’ canals through which atraumatic brain tissue decompression can be performed. The most striking complication, which occurred in one third of patients reported by Day, was post-operative oedema of the temporal lobe requiring ICU management. We agree with Dolenc [12] that venous drainage problems, related to extradural temporal lobe manipulation were probably the cause of the brain swelling. Retraction of oedematous parenchyma, chronically compressed by an underlying mass may precipitate postoperative oedema, infarction, and intracerebral haemorrhage. This holds particularly true with a huge meningioma. Indeed, in a previous paper by our group we showed a positive correlation between tumour size and extent of perifocal edemata. A positive correlation was also found between grade of oedema and cortical penetration [19]. Minimal retraction and preservation of the venous drainage are therefore crucially important. The extradural strategy described by Day [9] involves extensive temporal lobe manipulation, in which the undersurface of the temporal lobe is separated from the cavernous sinus wall. In our experience, the choice of the pterional transsylvian intradural approach resulted in venous drainage preservation and avoided frontal and temporal lobes damage from retraction. A satisfactory preservation of brain structural integrity was demonstrated by late follow-up FLAIR MR studies. We choose this particular sequence for its capability to show brain tissue oedema or degenerative and gliotic components more clearly than conventional T2-weighted and pro- Large sphenocavernous meningiomas: Is there still a role for the intradural approach via the pterional-transsylvian route? ton density-weighted images [22]. Its clinical usefulness in neuroimaging has been described in regard to several conditions [7, 22]. The frontal and temporal lobes ipsilateral to the approach consistently showed postoperative alterations consistent with permanent parenchymal gliosis. These changes, however, were of limited extent, were not associated with any specific neurological morbidity, and correlated well with the neurobehavioral outcome in this series. 3) A sphenocavernous meningioma usually spares the paraclinoid segment of the ICA and proximal control of this vessel can be safely achieved through a pure intradural strategy. In our experience the optic apparatus was frequently shifted and compressed, but never embedded in the tumour and it was always possible to dissect it free. Although the cisternal portion of the III nerve could be displaced, stretched, and rarely, half surrounded by the tumour it was always possible to dissect it free. A transient III nerve palsy was observed in three patients. One patient’s investigations showed an intracavernous component of the tumour which was not removed. We believe with others [15, 16, 20] that, in a giant tumour in which the main part responsible for the clinical features is extracavernous, operation should be directed at the extracavernous portion of the tumour. 4) None of our patients had a recurrence after undergoing a grade II resection. One patient, who had a subtotal resection (grade IVa), showed symptomatic tumour progression and required reoperation. These low rates of recurrence are based on an observation period averaging 42.3 months. Conclusions Large meningiomas arising from the dura covering the medial portion of the sphenoid bone, with or without invasion of the pericavernous and cavernous sinus structures, may be operated on adopting pure intradural resection tactics via the traditional pterional-transsylvian route. The major indications for this pure intradural approach are lateral growth of the tumour into the middle cranial fossa that limits the possibility of temporal lobe retraction, and a lack of frank cavernous sinus invasion. In our experience, the rates of gross total removal and surgical complications related to brain retraction or vascular manipulation are acceptable and not worse those reported for complex extra-intradural skull base approaches. These, on the other hand, still need validation based on long- 281 term follow-up evaluations for this group of meningiomas. We believe that the major hazards of perioperative morbidity in these patients are related to the intradural vascular and neural dissection phase, and these steps therefore represent the most important focus in defining the strategy for approaching these meningiomas. We conclude that, although contemporary skull base approaches, with intra and extradural strategies, represent the gold standard to approach cranial base meningiomas, the traditional intradural pterional transsylvian approach continues to have a role in the treatment of selected subgroups of cranial base tumours such as giant sphenocavernous meningiomas. References 1. Alaywan M, Sindou M (1993) Facteurs pronostiques dans la chirurgie des meningiomas intracrâniens. Rôle de la taille de la tumeur et de sa vascularisation artérielle d’origine piemérienne. Etude sur 150 cas. Neurochirurgie 39: 337–347 2. Al-Mefty O (1990) Clinoidal meningiomas. J Neurosurg 73: 840–849 3. Bonnal J, Thibaut A, Brotchi J, Born J (1980) Invading meningiomas of the sphenoid ridge. J Neurosurg 53: 587–599 4. Brotchi J, Bonnal JP (1991) Lateral and middle sphenoid wing meningiomas. In: Al Mefty O (ed) Meningiomas. Raven Press, New York, pp 413–425 5. 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Part I: the influence of tumour size, duration of symptoms, and microsurgery on surgical outcome in 101 consecutive cases. J Neurosurg 61: 633–641 Tsuchiya K, Mizutani Y, Hachiya J (1996) Preliminary evaluation of fluid-attenuated inversion-recovery MR in the diagnosis of intracranial tumours. AJNR 17: 1081–1086 Yamaki T, Tanabe S, Sohma T, Uede T, Shinya T, Hashi K (1988) Feeding arteries of parasellar meningiomas: angiographic study of medial sphenoid ridge and tuberculum sellae meningiomas. Neurol Med Chir (Tokyo) 28: 553–558 Yaşargil MG (1996) Microneurosurgery: microneurosurgery of CNS tumours. Georg Thieme Verlag, New York, vol. IVB, p 136 Comment This is a very well written paper on the surgical treatment of large spheno-cavemous meningiomas. The tenor of the article appeals because the authors go back to basics and prove in a convincing way that a well executed, straightforward pterional approach is very effective in treating these tumours. In the light of all the skull-base surgery violence it is a relief to find an article that points out the merits of such a time-honoured approach. The results presented are as least as good as the results in those studies where extensive portions of the skull-base were removed to get better access to the tumor, enabling the surgeon to carry out a more complete resection. In this respect the message of the paper is a very timely one since there seems to be a tendency among skull-base surgeons to perform much more limited resections than some years ago, because of the often very slow growth-rate of these meningiornas and because of the possibility to treat the remnant or the recurrence by way of stereotactic irradiation. The advice of the authors to expose the distal middle cerebral artery and its branches first before starting the removal of the tumor is well taken. However, in my opinion it might be advisable to delay the tumor-resection and to look for the intracranial portion of the Internal Carotid Artery and from there to follow the Middle Cerebral Artery in a distal direction. The extra time spent in performing these manoeuvres is well invested since when the operation has a poor outcome it is in the majority of cases caused by a lesion of the ICA or the MCA, or one of its branches. K. Tulleken Correspondence: Domenico d’Avella, M.D., Neurosurgical Clinic, Department of Neuroscience, Psychiatric and Anesthesiolgical Sciences, Policlinico Universitario, via Consolare Valeria 1, 98122 Messina, Italy.
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