| Home | E-Submission | Sitemap | Editorial Office |  
J Minim Invasive Spine Surg Tech > Volume 10(Suppl 2); 2025 > Article
Balamurali, Subramanian, Panneerselvam, and Venugopal: Minimally Invasive Versus Open Surgery for Intradural Extramedullary Spinal Cord Tumors: A Critical Analysis

Abstract

Objective

Minimally invasive surgery (MIS) has attracted increasing interest for the excision of intradural extramedullary (IDEM) spinal cord tumors. While open surgery is associated with excellent rates of gross total resection (GTR), minimal neurological deficits, and favorable quality of life outcomes, MIS provides potential benefits including reduced morbidity, less postoperative pain, decreased tissue damage, reduced blood loss, and accelerated recovery. This study aimed to evaluate the efficacy of MIS compared to open techniques for IDEM tumor excision by analysing clinical outcomes and procedural advantages.

Methods

This retrospective study included 80 patients who underwent surgery for IDEM tumors by a single surgeon between 2012 and 2019. Outcomes between MIS and open surgery were compared. Assessed parameters included intraoperative blood loss, operative duration, tumor location, postoperative visual analogue scale (VAS) scores, length of hospital stay, and time to return to work. The primary outcomes were GTR rates and complications; secondary outcomes comprised symptom relief and tumor recurrence. All patients were followed for at least 3 years. Statistical analysis was performed to evaluate differences between groups.

Results

Of the 80 patients, 38 underwent MIS and 42 underwent open surgery. MIS was associated with significantly reduced blood loss (65 mL vs. 240 mL, p<0.01) and shorter hospital stays (4.4 days vs. 6.8 days, p<0.01). Although operative times were initially longer for MIS (160 minutes vs. 130 minutes), this was attributed to the learning curve. GTR rates were similar between the groups (94.6% MIS vs. 96.4% open, p=0.46). There were no significant differences in rates of cerebrospinal fluid leak, infection, or neurological complications (p=0.32). Postoperative VAS scores showed significant improvement at 1 and 3 months in the MIS group, but differences were no longer evident at 1 year. No patient in either group required revision surgery within 3 years (p=0.33).

Conclusion

MIS for IDEM tumor excision offers distinct advantages over open surgery, including reduced morbidity and faster recovery, while achieving comparable long-term outcomes. With the implementation of advanced MIS techniques, results equal or surpass those of traditional open approaches.

INTRODUCTION

Intradural extramedullary (IDEM) spinal cord tumors, though rare, are a significant cause of morbidity, often resulting in progressive pain and neurological deficits that impact quality of life. Traditional surgical approaches for spinal cord tumor involve open procedures, which require extensive dissection and are associated with longer recovery times, increased blood loss, increased postoperative pain and added comorbidity. Recent advancements in minimally invasive surgery (MIS) techniques, particularly those utilizing tubular or expandable retractors, offer a less invasive alternative [1]. MIS approaches have demonstrated substantial benefits, including reduced blood loss, shorter hospital stays, and reduced postoperative pain management and long-term reduction in morbidity like instability and mechanical pain related to approach.
However, completeness of tumor resection, risks of neural retraction due to limited small exposure leading to poor outcomes, cerebrospinal fluid (CSF) leak-related complications have historically limited the widespread adoption of MIS in intradural tumor surgery [2]. In selected patients, MIS can achieve comparable to better resection rates to traditional open techniques, with added benefits of preserving spinal stability and biomechanics [3]. This study examines the surgical techniques, complications, patient selection, intraoperative and postoperative outcomes of intradural tumor surgeries aiming to establish MIS as a viable approach that minimizes morbidity and enhances recovery without compromising tumor excision or patient safety.

MATERIALS AND METHODS

1. Study Design and Patient Selection

This retrospective study aims to compare the intraoperative and postoperative parameters of patients operated with open and MIS technique for IDEM tumors. The patients were operated between September 2012 to September 2019. This study was approved by the Institutional Review Board, and written informed consent for participation and publication was obtained from all patients. A minimum follow-up of 3 years postsurgery are done in all patients, though some patients are in a longer follow-up. Patients lost to minimum follow-up of 3 years have been excluded from the study. Demographic date recorded include, name, age, sex, symptom duration, magnetic resonance imaging (MRI) images showing location type and extent of tumor, type of surgery MIS or open, intraoperative parameters like blood loss, duration of surgery, complications like CSF leak, infection or neurological deterioration and completeness of tumor resection from intraoperative observation and immediate postoperative scans. Tumor pathology was also noted. Postoperative duration of stay on hospital, return to normal activities, return to work, and postoperative pain visual analogue scale (VAS) were noted and documented on 3 months, 1 year, and 3 years.

2. Surgery Case Selection

MIS is suitable for IDEM lesions extending up to 2 vertebral body levels using expandable tubular retractors. For tumor spanning more than 3 levels, MIS and expandable retractors are not recommended in view of inadequacy of exposure. Hence open surgery is preferred. MIS can address ventrolateral or dorso-lateral lesions via lateral durotomy and allows for en bloc resection of schwannomas, neurofibromas, or piecemeal removal of meningiomas. If the tumor is placed completely ventral or dorsal then an open surgery was preferred by the surgeon. However, complete ventral or dorsal lesions are very rare. Open surgery was implemented in all lesions including those larger than 3 vertebral body levels or other reasons like cost of surgery, patients wish or factors against MIS approach. Dumbell lesions were treated by either method.

3. Inclusion Criteria

(1) Diagnosis: patients diagnosed with IDEM spinal tumor confirmed by imaging (MRI) and clinical evaluation
(2) Type of tumor: neurofibroma, schwannomas, meningiomas or mimics
(3) Location: cervical, thoracic and lumbar
(4) Levels: 3 vertebral body levels above or below
(5) Type: IDEM and dumbbell lesions extending to the foramina or extra foraminal region
(6) Age range: adults aged 18 years and older
(7) Tumor size: tumors suitable for removal through minimally invasive or traditional open surgical techniques
(9) Symptoms: patients with symptoms warranting surgical intervention, such as progressive pain, paraesthesia, neurological deficits, or spinal cord compression causing myelopathy.
(10) Minimum 3 years with visits at 3 months, 1 year, and 2 years with MRI follow-up immediately after surgery, 1, and 3 years.

4. Exclusion Criteria

(1) Prior spinal surgery: patients with a history of prior spinal surgeries or spinal fusion affecting the tumor site
(2) High-risk comorbidities: patients with severe cardiovascular, pulmonary, or other systemic conditions that contraindicate prolonged surgery
(3) Severe neurological deficits (American Spinal Injury Association Impairment scale - ASIA A or B) open surgery was preferred in this situation.
(4) Those lost to follow up or were not able to do MRI scans at 1 and 3 years.

SURGICAL TECHNIQUE

1. Equipment’s Needed for Surgery

1) Surgical instruments and retractors for MIS

Key tools include tubular retractor systems, either expandable or fixed, to minimize muscle disruption while maintaining a narrow surgical corridor. Serial dilators are employed for gradual tissue dilation, and a table-mounted retractor holder stabilizes the retractors [4]. Enhanced visualization is achieved with an operating microscope, while bayoneted micro-instruments, such as dissectors, forceps, and scissors, facilitate work within the confined surgical space. Bone removal and tissue access are optimized with high-speed drills and Kerrison rongeurs.

2) Tumor resection instruments

Tumor resection demands precision tools like ultrasonic aspirators for controlled removal with minimal tissue damage. Microsurgical suction tips manage bleeding and keep the field clear, while micro curettes and nerve root retractors safely mobilize or manipulate the tumor. Electrocautery devices, both bipolar and monopolar, ensure effective hemostasis in confined spaces.

3) Dural and closure instruments

For precise dural incisions, a No. 11 scalpel blade is essential, followed by dural closure with 5-0 or 6-0 polypropylene sutures to reduce the risk of CSF leakage [5]. Bayoneted needle holders, toothed forceps, and knot pushers facilitate accurate suturing in limited spaces. Dural sealants, fibrin glue, autologous fat grafts, or tensor fascia muscle pledgets further reinforce the closure and minimize CSF leakage risks.

4) Ancillary equipment

Hemostatic agents like surgical and Gelfoam provide additional bleeding control, while electrophysiological monitoring ensures the integrity of spinal cord and nerve root functions, particularly for complex cervical and thoracic tumor resections.

2. Minimally Invasive Surgery IDEM

The procedure begins with the patient in a prone position under general anesthesia and neuromonitoring. The target spinal level is confirmed using intraoperative x-ray imaging. After confirming the site, a vertical incision approximately 1.5–2 cm from the midline is made, based on pre operative MRI findings that determine the tumor’s extent and the appropriate retractor type fixed or expandable. The side of approach is based on the predominance of the tumor and direct approach to the tumor. In case it’s a midline tumor, then the most symptomatic side was chosen.
The subcutaneous tissue is dissected to expose the thoracolumbar fascia. Serial dilators are docked over the hemilamina to gently separate muscles from the underlying lamina, guided by lateral fluoroscopy to ensure precision. The final position is confirmed with anteroposterior and lateral images before placing the tubular retractor over the largest dilator. The retractor is angulated as needed and secured with a table-mounted holder.
An operating microscope which enhances visualization, providing the necessary depth perception for accurate dissection is used in all cases. Hemilaminectomy is performed using a high-speed drill and Kerrison punch, preserving critical structures like the spinous, interspinous, and supraspinous ligaments. The tube is angulated in such a way that the base of the spinous process is drilled to reach the midline. Simultaneously, the table is also tilted away from the surgeons to see the midline on the opposite side. After this step, the tube can be adjusted to the unilateral side or as required. Once the bony decompression is done, the ligamentum flavum is excised, and minimal medial facetectomy is performed to fully expose the lateral edge of the dura. Bayoneted instruments prevent visual obstruction, maintaining a clear surgical field.
The dura mater is opened longitudinally away from the midline in an lateral position with a No. 11 scalpel blade, and 6-0 polypropylene tack sutures hold it open. The arachnoid membrane is carefully incised to reveal the spinal cord, nerve roots, and tumor. The surgical approach, whether en bloc resection or piecemeal removal depends on the tumor’s characteristics, including size, dural attachment, and origin. The full extent of the tumor must be visualized from cranial to caudal before micro resection of tumor is started. An ultrasonic aspirator may be used to fragment and aspirate the tumor while minimizing damage to surrounding tissues. Meticulous dural closure is critical to prevent CSF leaks. Continuous or interrupted sutures are employed using fine bayoneted toothed forceps and needle holders. We prefer continuous sutures for watertight closure. Fibrin sealant is applied to reinforce the repair only if there is a suspicion of CSF leak from an inadequate closure. Valsalva mauver is used at the end of the procedure to check the adequacy of the closure. The tubular retractor is carefully removed, muscles are reapproximated, and fascia is closed followed by subcutaneous tissue with 3-0 vicryl sutures. The skin is closed using continuous nonabsorbable sutures to ensure a watertight seal.

3. Open IDEM

In open surgery the spine is exposed midline to expose the tumor to its full extend cranial and caudally. The muscles are stripped on both sides to expose the spine process and the lamina. The spinous process is removed along with the attachments and a complete laminectomy is done to expose the dura. The facet joints are not disturbed, but sometimes medial facet removal may be required, depending on the size of the tumor. Dumbbell lesions may necessitate unilateral facet removal in order to expose the tumor in the foraminal region. Following this epidural hemostasis is achieved, and the dura is opened in the midline to expose the tumor. The full extent of the tumor is assessed and depending on whether it is a schwannoma, neurofibroma, or meningioma, the tumor is excised accordingly. If it is a meningioma, then the dura is treated with diathermy and the arachnoid is removed completely. Meticulous closure of the dura is achieved with continuous nonabsorbable 6-0 proline. The fascia is closed with 2.0 vicryl and subcutaneous closure is done with 3-0 vicryl. The skin is closed with nonabsorbable continuous 3-0 ethilon.

4. Feasibility of MISS in IDEM Tumor Resection

Minimally invasive spine surgery (MISS) technique can be effectively employed in selected cases of IDEM tumors. MISS is ideally suited for tumors that: (1) involve 1–2 vertebral levels with well-demarcated margins; (2) are located laterally or dorsolaterally (such as schwannomas or meningiomas with lateral dural attachment); (3) are noncalcified, soft-tissue tumors amenable to piecemeal or en bloc resection; (4) have minimal extradural extension; and (5) are in patients with good general condition, suitable for longer operative duration under general anesthesia.
On the other hand, MISS is contraindicated or less favorable in: (1) tumors involving more than 3 vertebral levels; (2) midline ventral tumors with broad dural attachment, limiting safe resection via narrow corridors; (3) calcified or highly adherent meningiomas with complex vascular involvement; (4) very large dumbbell tumors requiring extensive foraminal or extraforaminal dissection and stabilization, and; (5) patients with severe neurological deficits (ASIA A/B) where rapid and wide decompression is required.
Hence, careful preoperative assessment of tumor morphology, location, extension, and patient factors is essential to determine suitability for MISS. The surgeon’s experience and availability of advanced instrumentation also play a key role in decision-making.

RESULTS

The study group consisted of 80 consecutive patient who met the inclusion criteria. They were included in the MIS or open group based on the preference of the surgeon, cost to treatment and other multiple factors favoring one of the techniques as discussed earlier in the inclusion criteria for MIS tumors. The patients included was 38 in the MIS group and 42 in the open group. The mean age was similar in both the groups with 44.5 and 48.6 years, and sex range was also similar, 62% and 54% men in the MIS and open groups respectively. The most common symptom in both groups was pain in the legs (86%), low back pain (42%), paraesthesia (36%), and difficulty in walking (20%).
The demographic data (Table 1) shows that the patients majority of the open cases involved the cervical spine (52%) and MIS group had equal number of cases in the cervical and lumbar (42%). As planned, no one above 3 levels were attempted with MIS and were operated by open method (32.5%). Most cases in the MIS group were limited to the 1 vertebral level only (71%). The type of tumors were schwannomas (50%), neurofibromas (22.5%), and meningiomas (25%), others were extramedullary myxopapillary ependymoma and paraganglioma (2.5%).
Intraoperative finding is summarized in Table 2. Operative time was higher in the MIS group than the open due to the initial learning curve (180 minutes vs. 130 minutes, p<0.03). Surgical blood loss was significantly lower in the MIS group (average, 65 mL; range, 50–110 mL) compared with the open group (average, 240 mL; range, 200–800 mL) (p<0.01). Gross total resection (GTR) of tumor was achieved equally good in both methods in 94.6% MIS cases and 96.4% in open cases. In the open surgery group 5 patients (12%) had an unilateral approach which signifies that tumors can be removed unilateral laminectomy open also. Of the 4 incomplete resections (9.5%) in the open group, 2 were large dumbbell lesions, where, the extradural component was not completely resected and small lesion was left in the thoracic cavity region in one case and cervical brachial plexus in the other. The other 2 cases were a meningioma and a myxopapillary ependymoma with incomplete resection. In the MIS group of 2 patients (5.5%), one was a dumbbell cervical lesion and a meningioma in the thoracic level. Lumbar drain was used in one open case where there was a small dural leak after a dural closure from the suture entry point. The lumbar drain was removed on the 7th day. No patient in both the groups had a would drain. The mean hospital stay in the MIS group was (4.4 days) compared with the open group (6.8 days). The return to normal activity was 12 days for MIS and >32 days for open (p<0.03). There was no significant difference in the complication of CSF leak, would infection and neurological complications in both groups (p=0.7). No patient was reoperated at 3 years (p=0.33). Pre and postoperative VAS scores were significantly different at 1 month and 3 months but the difference declined at 1 year and 3 years.

DISCUSSION

The occurrence of intradural spine tumors is rare, which is about 5 to 10 cases per 1,000,000 people. Usually these tumors are benign, which can cause progressive pain or neurological deficit. The most common IDEM tumors of the spine are meningiomas, schwannomas and neurofibromas. Cervical and thoracic tumors present with neck pain or upper back pain and whereas lumbar tumors are associated with lower back pain, leg pain, lower extremity weakness or bowel and bladder dysfunction [6]. The principal objective for surgery in patients with spinal tumors is complete tumor excision, decompression of spinal cord, avoid neurological worsening and restoration of mechanical stability. The traditional open resection involves a large midline incision, extensive muscle dissection, and bilateral laminectomies. MIS utilizes a small paramedian incision and unilateral muscle splitting with tubular retractors, significantly reducing soft-tissue damage [4]. Studies have shown comparable GTR rates between MIS and open surgery, with MIS achieving GTR rates up to 92.6% [6]. Though MISS has gained popularity and adapted in degenerative spine disease, the use in tumor surgery is still not accepted widely due to proposed risk of incomplete tumor removal, neural retraction and damage, inadequate dural closure and CSF leak-related complications. MIS technique has been associated with reduced blood loss, infection rate, complications, hospital stay, improved post of pain control, faster recovery along with complete resection of tumor with reduced complications and morbidity and lower CSF leak rates [7]. Similar patient demographics and tumor presentations was seen in our study. Current literature states that one of the main deciding factors of the outcome was the extent of the tumor above 3 vertebral bodies and the surgeons experience [8].
Whatever method was chosen adherence to fundamental neurosurgical principles is essential to minimize complications during tumor removal. Several measures are taken to reduce the risk of peri and postoperative complications [9]. Intraoperative strategies include proper patient positioning to prevent peripheral nerve compression, use of electrophysiological monitoring especially D wave pattern and accurate placement of the tubular retractor is crucial to ensuring adequate exposure of the entire tumor and avoid the need for extending the incision [10]. A wide dural opening minimizes manipulation of the spinal cord and nerve roots. Key considerations for tumor excision include gentle handling of neural structures, adequate exposure of the tumor margins, meticulous hemostasis, progressing from normal to pathological tissue and using appropriate microsurgical instruments and techniques, such as ultrasonic aspirators which reduces the risk of neural injury [11]. We routinely use the ultrasonic curator for all types of tumors at different setting to remove the tumor which improves safety and duration of surgery. The closure of dura should be done meticulously, and if required, autologous fat grafts [5], synthetic materials and fibrin sealants were used, otherwise it can lead to post op CSF leak and complications [12]. Use of U-clips or titanium clips can facilitate dural closure without knot tying. CSF leaks can lead to pseudo-meningocele formation, meningitis, and impaired wound healing [13]. They occur in approximately 18% of intradural tumor surgeries. Each type of tumor excision needs special considerations as described below [14,15].

1. Meningioma (Figure 1)

Meningiomas arise from arachnoid cap cells and usually present from around the nerve root sleeve and laterally which makes it convenient for MIS approach from unilateral side. Those arising from the ventral or dorsal midline have their origin from dural fibroblast or the pia. These can be a relative contraindication for MIS approach however they are seldom rare. When there is dural tail sign which may be seen in 30%–50 % of cases the exposure must include up to the end of the tail to remove the tumor fully. The most common types of meningiomas are meningothelial and psammomatous variety. Gross total excision may sometimes not be possible because of the strong adherence with the dura, calcification or ventral attachment not accessible to remove completely. In meningiomas, GTR involves excising the tumor and coagulating the dural attachment. If part of the tumor is adherent to nerve roots or the spinal cord, a near-total resection may be performed to avoid neurological deficits. Aggressive dural resection and reconstruction is not recommended as the recurrence rates are no different from just a dural coagulation [16-18] and higher complications. The spinal meningiomas are less aggressive than the cranial and hence long-term follow-up of recurrence rate is reported to be less than 15% [16,17,19,20]. Radiotherapy is reserved only for the recurrent tumors that cannot be resected and malignant tumors which are extremely rare.

2. Schwannoma (Figure 2)

These tumors arise from the Schwann cells of the posterior roots and hence they tend to be in the posterolateral region. Rarely they may extend extradural or seen intramedullary [18,21]. Small and medium sized tumors can be removed completely as they are well capsulated and tend to arise from a single fascicle and usually the sensory root [18,22]. If the tumor is large an intracapsular debulking is done and then the fascicle and tumor are disconnected and removed fully. If a single fascicle is not identified then the fleshy part of the tumor is removed completely and capsule if left behind. Aggressive removal of the tumors versus the risk of neurological damage must be assessed in large tumors and in tumors where multiple fascicles are attached. By intracapsular debulking the patient is relieved of his symptoms and the peripheral nerve function are also intact. These incomplete tumors removals remain dormant and asymptomatic for many years [18]. However, in the setting of neurofibromatosis (NF) usually type 2 the recurrence rates are 39% at 5 years and 6%–12% in those less than 5 years [21-23]. The occurrence rate of postoperative neuropathic pain is as high as 7.2 %. In intradural tumor removal, especially in nerve sheath tumor there is loss of Schwann cell guidance leading to random sprouting of neurons causing the neuropathic pain [24]; this is also seen with other intradural tumors like meningioma and ependymoma [25]. There is an underestimation in assessing the long-term disabilities like neuropathic pain in tumor patients who are likely in need of pain medication [9]. This can be managed by very careful microsurgical technique when removing the tumor respecting tumor planes.

3. Neurofibroma and Dumbbell Lesions (Figure 3)

Unlike schwannomas the cell origin is not defined for a neurofibroma and may arise from mesenchymal lines. Up to 60% are associate with NF type 1 [18]. Though majority of these are intradural about 30% can be dumbbell lesion with an extradural component. These tumors can become extremely large before they can present with symptoms. Sometimes the extradural component in the thoracic region can be very large entering the pleural cavity. Some of the large intradural tumors cause a fusiform enlargement of the tumor which makes it difficult to spare the nerve [26]. In this setting sacrificing the nerve is not always associated with a neurological deficit [18]. The recurrence rate in these tumors is expected to be about 12% [27]. With MIS technique, the tube is first directed at removing the intradural component and then tilting the tube to get the extradural component [28]. The facet joints have to be sacrificed to remove the tumor which may have scalloped the foramen. It is also possible to remove the tumor without completely removing the facet and working around the tumor from both sides, as we had done in one of our cases; to avoid instrumentation. With MIS in our series, we have not done instrumentation for instability. Dural closure is very difficult and CSF leaks are common in this category of tumors. There is increase chance of CSF leak in the thoracic cavity due to the negative pressure if there is an incomplete removal following dumbbell tumor removal.
In our study, we noticed that the demographic results were similar in patients age, sex, and presentation. This retrospective study has a patient selection bias for the type of operative procedure based on the patient factors and surgeons’ preference. The patient factors were the cost of surgery, as MIS was more expensive, some patients preferred open surgery. Some patients had significant co morbidities and since MIS has a slight longer operating time they were opted for open surgery. The surgeon factors were the choice of approach based on the tumor location, more dorsal placed tumors were preferred for open, between 2–3 vertebral bodies were operated open in the initial phase as the tubular retractor will only expand to 3 vertebral bodies. Meningiomas needed exposure of the dural tail extending beyond the preferred opening [29]. If the radiological diagnosis was certain to be a schwannoma, but extending just beyond 3 vertebral levels or borderline, they were operated by tube as the tumor can be debulked with ultrasonic aspirator and shrunk to deliver it within the space created in the expandable tube. Dumbbell tumors with a large extradural extension were preferred open approach as they needed fixation, and the very large size lesions needed larger exposure. In the later part, these were also operated by MIS with complete GTR of tumor. This emphasizes the fact that the MIS tumor operations have a steady learning curve without compromising on the surgical outcome [27]. Interestingly the commonest location of tumors in our study were cervical spine (47.5%) as compared to most studies where lumbar level tumors were more common. Majority of single vertebral tumors (71%) were operated by MIS technique. The duration of symptoms was seen to be more with the open group (11.2 months). Of the 27 patients who had a single level vertebral tumor were mostly schwannomas and had a duration of presentation of 9.4 months. Those who presented with less duration of symptoms had larger tumors mostly in the lumbar (58%) and cervical (30%) regions.
A subgroup analysis of the MIS group showed that the patient selection in the initial phase of the study was restricted to 1–2 level tumors and then later larger lesions were also approached. The operative time was longer in the MIS group in the initial phase compared to the later cases where the duration became like open. Other factors like blood loss, GTR, and complications were similar. There were no neurological deficits on the MIS group. Residual tumors were seen in 4 open cases and 2 MIS cases in the MRI taken within 24 hours of surgery. The reason for the residual tumors were the large size of the extradural neurofibroma component in 2 cases, dural adhesion in case of a meningioma in 2 cases and adherence to the conus in a myxopapillary ependymoma in 1 case and a neurofibroma that was inadequately removed around the conus. These tumors were followed up and one of the cases showed a slight increase in size radiologically at 3 years in the MIS group but then patient did not want further surgery, and the patient is under follow-up. The author generally does not use wound drains for IDEM tumor excision surgery [23]. In one case where a CSF leak was present despite meticulous attempt to close the dura, a lumbar drain was used for 7 days and wound healed without any complications. Lumbar drains should be placed in the level higher where possible though a separate opening and not through the same opening for the procedure. The reason for this is the possibility of CSF leaking into the wound be due to negative suction pressure in the surgical cavity.
Significant differences (p<0.05) were seen between the groups in intraoperative blood loss, postoperative stay in hospital, return to work, and normal activities with superiority for MIS approach. However, the duration in the surgery group was higher in the MIS group and was attributed to the learning curve in the initial phase. This is variable in the literature also [6,7]. The primary outcomes of the study were GTR and complications (Table 3), which was not different in both groups. Several studies have used MIS technique and achieved 100% GTR rates [30-33], without any serious complications. The literature suggests that GTR in open approaches ranges from 74% to 92% of cases [31-33]. The MIS or mini-open techniques have achieved similar rates of GTR in the literature, ranging from 80% to 94% [30,32]. Similar results were reported by Wong et al. [1,6] with both open and MIS technique the GTR ranges from 80% to 90% in another study of Wong et al. [1,6] attained GTR of 92.6% using true MIS approach. Another advantage of using MIS is reduced CSF leak percentage which is about 0 to 5%. In a study by Thavara et al. [34], GTR was achieved in 67% of cases and NTR in 33% cases. In our experience there was no difference in the GTR rates between groups. The one patient in the MIS group with incomplete resection showed a small increase in size of the lesion and is being managed by observation as patient is asymptomatic.
The main complication that is concerning most surgeons adopting this technique is CSF leak and, in our series, we had no CSF leak in the MIS group and no lumbar drain was used. Though dural closure is technically challenging through tubes it becomes easy with experience. We perform a Valsalva manuver at the end of the procedure and if we see a CSF leak, we either use lumbar drain or dural sealants. Following the MIS technique once the tubes are removed the soft-tissue planes oppose and the muscle planes collapse causing a tamponade effect with no dead space for CSF collection and pseudomeningoceal. Lumbar drain was not needed in any case and in one case a dural sealant was used for CSF leak from the suture entry site but this did not result in a CSF leak post op. In open surgery 0%–9% CSF leak rate was reported [30,31]. In the open group, 1 patient required a lumbar drain but no repair or resurgery was required. No patients in the MIS group had blood transfusion and the average Blood loss was about 65 mL (p<0.01). This is because of the muscle splitting and tamponade by the tube during the procedure. Similar results have been reported in other cases compared to open surgery with 115 mL [34]. One patient in the open group needed a blood transfusion 2nd postoperative day. Surgical site infection (SSI) was seen in 1 patient with open surgery. In the open case, 1 SSI needed a would debridement and readmission after discharge. Neurological deficit was seen equal in both patients with minor sensory and motor deficits. The patients in the open group developed sensory numbness in foot and in another patient was worsening of foot weakness by one grade. This weakness improved to normal in 3 months. In the MIS group, similar mild weakness of thigh was seen following a dumbbell lesion that was excised but no significant disability was seen. This deficit has persisted at 3 years possibly due to nerve injury of L3 during removal. Tumors arising from the cord level have a higher risk of neurological injury compared to those at the lumbar level where the roots have a higher tolerance to manipulation [35]. MIS unilateral approach uses a paramedial dural incision which provides a corridor to see the lateral aspect of the cord and roots avoiding cord manipulation and hence reduced neurological damage [1,5,30]. The neurological deficits are more common in the upper thoracic cord region due to the watershed zone [35]. There was no significant difference in the complication of CSF leak, would infection and neurological complications in both groups (p=0.7).
The secondary outcomes including impact of surgery on symptom relief and tumor recurrence. Increased hospital stay postsurgery is likely due to excessive pain, slow mobility, prolonged antibiotics and lumbar or wound drain. In MIS because of reduced soft-tissue damage the postoperative pain is less and patients mobilized earlier and require less postoperative analgesia and are discharged from hospital earlier. Avoiding a lumbar drain speeds up the discharge process significantly allowing patients to go home by average of 4.4 days (3.5–6.6 days) postoperative (p<0.02). Similar finding is seen reported in the literature for both groups (2.3–4.9 days vs. 4.1–6.3 days) [31,32,36,37]. Similarly return to normal activities including self-care in activities of daily living, toileting, walking inside house and eating in sitting position was seen at 12 days for MIS and >32 days for open (p<0.03). Return to work was seen as another advantage of MIS patients. In our series, all patients returned to work ranging from desk top job to manual labor in 22 days (16–32 days) compared to patients in the open group at average of 45 days (18–94 days).
No patient was reoperated at 3 years (p=0.33). Pre- and postoperative VAS scores were significantly different at 1 month and 3 months but declined at 1 year and 3 years. This highlights that early discharge from hospital, early return to work is an important indicator and is directly related to improved VAS scores up to 3 months, no neurological deficits and complications. Hence MIS patients fare better than the open surgery group upto 3 months. Some of the outcomes not measure is work productivity, financial losses, psychological wellness, improved fitness and long-term prevention of degeneration and back pain postsurgery. It is only logical to conclude that in the immediate phase MIS is superior to open and the long-term results, not measured, are still in favor of MIS in a selective group of patients. Safe GTR of tumors is still the best measure of long-term outcome and we propose to present our results in 5 and 10 years.
One of the major limitations of this study is the section bias in choosing larger (>3 vertebral body levels) and more complex tumors in the cervical and upper thoracic region for open surgery compared to the smaller lesions (<3 vertebral bodies) with more preference in the lumbar level for MIS. However, using a multivariant statistical analysis between the 2 groups showed no significant different in the neurological outcome in both the groups. Absence of a randomized study highlights the complexity of designing such a comparison. If only tumors less than 3 vertebral bodies were compared with the 2 groups still MIS is similar or superior in terms of primary and secondary outcomes.

CONCLUSION

The MIS technique for IDEM spinal tumor removal offers numerous advantages over traditional open surgery, including GTR of tumor, lower complication rates, and faster patient recovery early return to normal activities and work. By adhering to meticulous surgical principles and utilizing advanced technologies, surgeons can effectively manage IDEM tumors with outcomes comparable and superior to open techniques. This study highlights that in tumors less than 3 vertebral body levels MIS has superior results in several parameters compared to open surgery. Though the study is a retrospective critical analysis of the data available we feel a prospective study selecting similar size and character of tumor will show similar results favoring MIS based on a subgroup analysis.

NOTES

Conflicts of interest

The authors have nothing to disclose.

Funding/Support

This study received no specific grant from any funding agency in the public, commercial, or not-for-profit sectors.

Figure 1.
Pre- and postoperative magnetic resonance imaging (MRI) of a patient diagnosed with meningioma. (A) Postcontract MRI sagittal view showing heterogenous enhancing intradural extramedullary lesion at C7–T1. (B) Postcontract MRI axial view showing an enhancing intradural extramedullary lesion at C7–T1 with left dorsolateral predominance and severe cord compression. (C) Postoperative MRI sagittal view showing no enhancing residual lesion suggestive of complete tumor resection. (D) Postoperative MRI axial view showing complete tumor resection and the soft-tissue plane of approach from left side.
jmisst-2025-02159f1.jpg
Figure 2.
Pre- and postoperative magnetic resonance imaging (MRI) of a patient diagnosed with C3 Schwannoma. (A) MRI cervical spine sagittal views showing an enhancing intradural extramedullary lesion at anterior aspect of C3. (B) MRI axial view showing an enhancing intradural extramedullary lesion (arrow pointing) at C3 with right neural foraminal extension and severe cord compression. (C) Postoperative MRI sagittal views showing complete tumor resection with absent residue. (D) Postoperative MRI axial view showing complete tumor resection and the soft-tissue plane of approach from right side.
jmisst-2025-02159f2.jpg
Figure 3.
Pre- and postoperative magnetic resonance imaging (MRI) of a patient diagnosed with L4 neurofibroma. (A) MRI lumbar spine sagittal views showing an intradural extramedullary lesion at L4. (B) MRI axial view showing an intradural extramedullary lesion at L4 with severe canal and right side foraminal stenosis. (C) Postoperative MRI sagittal views showing complete tumor resection with absent residue. (D) Postoperative MRI axial view showing complete tumor resection and the soft-tissue plane of approach from right side.
jmisst-2025-02159f3.jpg
Table 1.
Demographic data in 80 patients with intradural extramedullary tumors
Variable Open (n=42) MIS (n=38)
Age (yr) 44.5 (32–79) 48.6 (26–82)
Spinal level
 Cervical 16 (38.1) 22 (57.9)
 Thoracic 10 (23.8) 7 (18.4)
 Lumbar 16 (38.1) 9 (23.7)
No. of spinal levels
 1 6 (14.3) 27 (71.1)
 2 10 (23.8) 11 (28.9)
 ≥3 26 (61.9) 0 (0)
Duration of symptoms (mo) 11.2 6.6
Pathology
 Neurofibroma 10 (23.8) 8 (21.1)
 Schwannoma 18 (42.9) 22 (57.9)
 Meningioma 12 (28.6) 8 (21.1)
 Others 2 (4.8) 0 (0)

Values are presented as mean (range) or number (%).

MIS, minimally invasive surgery.

Table 2.
Intraoperative data in 80 patients with intradural extramedullary tumors
Variable Open (n=42) MIS (n=38)
Approach
 Unilateral 5 (11.9) 38 (100)
 Bilateral 37 (88. 1) 0 (0)
GTR (postoperative MRI)
 No 4 (9.5) 2 (5.26)
 Yes 38 (90.5) 36 (94.7)
Lumbar drain 1 (2.4) 0 (0)
Fusion
 No 41 (97.6) 38 (100)
 Yes 1 (2.4) 0 (0)
Intraoperative blood loss (mL) 240 (200–800) 65 (50–110)
Operative time (min) 130 (80–480) 180 (90–340)

Values are presented as number (%) or mean (range).

MIS, minimally invasive surgery; GTR, gross total resection; MRI, magnetic resonance imaging.

Table 3.
Complications and postoperative outcome in 80 patients with intradural extramedullary tumors
Variable Open (n=42) MIS (n=38)
Complications after surgery
 Surgical 6 (14.3) 3 (7.9)
 Medical 2 (4.8) 1 (2.6)
Surgical complications
 CSF leak 1 (2.4) 0 (0)
 Surgical site infection 1 (2.4) 0 (0)
 Neurological worsening (motor, sensory) 2 (4.8) 2 (5.3)
 Others 1 (2.4) 0 (0)
CSF needing repair 0 (0) 0 (0)
Lumbar drain for CSF leak 1 (2.4) 0 (0)
Reoperation for tumor (in 3 yr) 0 (0) 0 (0)
Wound infection requiring resurgery 1 (2.4) 0 (0)
Mean hospital stay (day) 6.8 4.4
Mean return to normal activities (day) >32 12
Mean return to work >45 22
VAS score (overall)
 Preoperative 6.5 6.8
 3 Months 3.7 2.3
 1 Year 2.2 1.4
 3 Years 1.23 1.12

Values are presented as number (%) or mean (range).

MIS, minimally invasive surgery; CSF, cerebrospinal fluid; VAS, visual analogue scale.

REFERENCES

1. Wong AP, Lall RR, Dahdaleh NS, Lawton CD, Smith ZA, Wong RH, et al. Comparison of open and minimally invasive surgery for intradural-extramedullary spine tumors. Neurosurg Focus 2015;39:E11.
crossref
2. Lenschow M, Perrech M, Telentschak S, von Spreckelsen N, Pieczewski J, Goldbrunner R, et al. Cerebrospinal fluid leaks following intradural spinal surgery-Risk factors and clinical management. Front Surg 2022;9:959533.
crossref pmid pmc
3. Raygor KP, Than KD, Chou D, Mummaneni PV. Comparison of minimally invasive transspinous and open approaches for thoracolumbar intradural-extramedullary spinal tumors. Neurosurg Focus 2015;39:E12.
crossref
4. Kim YB, Hyun SJ. Clinical applications of the tubular retractor on spinal disorders. J Korean Neurosurg Soc 2007;42:245–50.
crossref pmid pmc
5. Syal A, Cozzi FM, Vazquez S, Spirollari E, Naftchi AF, Das A, et al. Dural closure techniques and cerebrospinal fluid leak incidence after resection of primary intradural spinal tumors: a systematic review. Clin Spine Surg 2024;37:291–5.
crossref pmid
6. Lee LY, Idris Z, Beng TB, Young TY, Chek WC, Abdullah JM, et al. Outcomes of minimally invasive surgery compared to open posterior lumbar instrumentation and fusion. Asian J Neurosurg 2017;12:620–37.
crossref pmid pmc
7. Cofano F, Giambra C, Costa P, Zeppa P, Bianconi A, Mammi M, et al. Management of extramedullary intradural spinal tumors: the impact of clinical status, intraoperative neurophysiological monitoring and surgical approach on outcomes in a 12-year double-center experience. Front Neurol 2020;11:598619.
crossref pmid pmc
8. Helal A, Yolcu YU, Kamath A, Wahood W, Bydon M. Minimally invasive versus open surgery for patients undergoing intradural extramedullary spinal cord tumor resection: a systematic review and meta-analysis. Clin Neurol Neurosurg 2022;214:107176.
crossref pmid
9. Lee SM, Cho YE, Kwon YM. Neurological outcome after surgical treatment of intramedullary spinal cord tumors. Korean J Spine 2014;11:121–6.
crossref pmid pmc
10. Costăchescu B, Niculescu AG, Iliescu BF, Dabija MG, Grumezescu AM, Rotariu D. Current and emerging approaches for spine tumor treatment. Int J Mol Sci 2022;23:15680.
crossref pmid pmc
11. Ali R, Hagan MJ, Shaaya E, Leary OP, Feler J, Bajaj A, et al. Endoscopic techniques for spinal oncology: a systematic literature review. Int J Spine Surg 2023;17:343–9.
crossref pmid
12. Fang Z, Tian R, Jia YT, Xu TT, Liu Y. Treatment of cerebrospinal fluid leak after spine surgery. Chin J Traumatol 2017;20:81–3.
crossref pmid pmc
13. Jiang L, Budu A, Khan MS, Goacher E, Kolias A, Trivedi R, et al. Predictors of cerebrospinal fluid leak following dural repair in spinal intradural surgery. Neurospine 2023;20:783–9.
crossref pmid pmc pdf
14. Miscusi M, Polli FM, Forcato S, Ricciardi L, Frati A, Cimatti M, et al. Comparison of minimally invasive surgery with standard open surgery for vertebral thoracic metastases causing acute myelopathy in patients with short- or mid-term life expectancy: surgical technique and early clinical results. J Neurosurg Spine 2015;22:518–25.
crossref pmid
15. Ito K, Aoyama T, Nakamura T, Hanaoka Y, Horiuchi T, Hongo K. Novel dural incision and closure procedure for preventing postoperative cerebrospinal fluid leakage during the surgical removal of dumbbell-shaped spinal tumors: technical note. J Neurosurg Spine 2016;25:620–5.
crossref pmid
16. Levy WJ Jr, Bay J, Dohn D. Spinal cord meningioma. J Neurosurg 1982;57:804–12.
crossref pmid
17. Solero CL, Fornari M, Giombini S, Lasio G, Oliveri G, Cimino C, et al. Spinal meningiomas: review of 174 operated cases. Neurosurgery 1989;25:153–60.
crossref pmid pdf
18. Spinal cord and spinal column tumors: principles and practice. AJNR Am J Neuroradiol 2007;28:394–5.

19. Roux FX, Nataf F, Pinaudeau M, Borne G, Devaux B, Meder JF. Intraspinal meningiomas: review of 54 cases with discussion of poor prognosis factors and modern therapeutic management. Surg Neurol 1996;46:458–63; discussion 463-4.
crossref pmid
20. Nittner K. Spinal meningiomas, neurinomas, and neurofibromas and hourglass tumours. In: Vinken P, Bruyn B, editors. Handbook of clinical neurology. American Elsevier; 1976. p. 177–322.

21. Schick U, Marquardt G, Lorenz R. Recurrence of benign spinal neoplasms. Neurosurg Rev 2001;24:20–5.
crossref pmid pdf
22. Seppälä MT, Haltia MJ, Sankila RJ, Jääskeläinen JE, Heiskanen O. Long-term outcome after removal of spinal schwannoma: a clinicopathological study of 187 cases. J Neurosurg 1995;83:621–6.
crossref pmid
23. Lot G, George B. Cervical neuromas with extradural components: surgical management in a series of 57 patients. Neurosurgery 1997;41:813–20; discussion 820-2.
crossref pmid
24. Butenschoen VM, Nehiba A, Meyer B, Wostrack M. Neuropathic pain after spinal intradural benign tumor surgery: an underestimated complication? Neurosurg Rev 2022;45:2681–7.
crossref pmid pmc pdf
25. Raco A, Esposito V, Lenzi J, Piccirilli M, Delfini R, Cantore G. Long-term follow-up of intramedullary spinal cord tumors: a series of 202 cases. Neurosurgery 2005;56:972–81; discussion 972-81.
pmid
26. Ferreira Filho AC, Blanco CMB, Trindade JVC, Mattos GB, Joaquim AF. Surgical outcome of spinal schwannoma and neurofibroma. Rev Assoc Med Bras (1992) 2023;69:e20230190.
crossref pmid pmc
27. Beighley A, Zhang A, Huang B, Carr C, Mathkour M, Werner C, et al. Patient-reported outcome measures in spine surgery: A systematic review. J Craniovertebr Junction Spine 2022;13:378–89.
crossref pmid pmc
28. He Z, Li CY, Mak CH, Tse TS, Cheung FC. Minimally invasive tubular retractor surgery for intradural extramedullary spinal tumor reduces postoperative degeneration of paraspinal muscle. Asian J Neurosurg 2022;17:74–84.
crossref pmid pmc
29. Takamiya S, Malvea A, Ishaque AH, Pedro K, Fehlings MG. Advances in imaging modalities for spinal tumors. Neurooncol Adv 2024;6(Suppl 3):iii13–27.
crossref pmid pmc pdf
30. Nzokou A, Weil AG, Shedid D. Minimally invasive removal of thoracic and lumbar spinal tumors using a nonexpandable tubular retractor. J Neurosurg Spine 2013;19:708–15.
crossref pmid
31. Tredway TL, Santiago P, Hrubes MR, Song JK, Christie SD, Fessler RG. Minimally invasive resection of intradural-extramedullary spinal neoplasms. Neurosurgery 2006;58(1 Suppl):ONS52–8; discussion ONS52-8.
crossref pmid
32. Zong S, Zeng G, Du L, Fang Y, Gao T, Zhao J. Treatment results in the different surgery of intradural extramedullary tumor of 122 cases. PLoS One 2014;9:e111495.
crossref pmid pmc
33. Mirimanoff RO, Dosoretz DE, Linggood RM, Ojemann RG, Martuza RL. Meningioma: analysis of recurrence and progression following neurosurgical resection. J Neurosurg 1985;62:18–24.
crossref pmid
34. Thavara BD, Kidangan GS, Rajagopalawarrier B. Analysis of the surgical technique and outcome of the thoracic and lumbar intradural spinal tumor excision using minimally invasive tubular retractor system. Asian J Neurosurg 2019;14:453–60.
crossref pmid pmc
35. Mehta AI, Adogwa O, Karikari IO, Thompson P, Verla T, Null UT, et al. Anatomical location dictating major surgical complications for intradural extramedullary spinal tumors: a 10-year single-institutional experience. J Neurosurg Spine 2013;19:701–7.
crossref pmid
36. Haji FA, Cenic A, Crevier L, Murty N, Reddy K. Minimally invasive approach for the resection of spinal neoplasm. Spine (Phila Pa 1976) 2011;36:E1018–26.
crossref pmid
37. Levy WJ, Latchaw J, Hahn JF, Sawhny B, Bay J, Dohn DF. Spinal neurofibromas: a report of 66 cases and a comparison with meningiomas. Neurosurgery 1986;18:331–4.
crossref pmid
About |  Browse Articles |  Editorial Policy |  For Contributors
Editorial Office
Department of Neurosurgery, Harrison Spinartus Hospital Chungdam
646 Samseong-ro, Gangnam-gu, Seoul 06084, Korea
TEL: +82-2-6003-9767    FAX: +82-2-3445-9755   E-mail: office@jmisst.org
Publisher
Korean Minimally Invasive Spine Surgery Society
350 Seocho-daero, Seocho-gu, Seoul 06631, Korea
TEL: +82-2-585-5455    FAX: +82-2-523-6812   E-mail: komisskomiss@komiss.org
Copyright © Korean Minimally Invasive Spine Surgery Society.                 Developed in M2PI