Journal of Pediatric Neurosciences
ORIGINAL ARTICLE
Year
: 2012  |  Volume : 7  |  Issue : 1  |  Page : 1--3

Pediatric spinal schwannomas: An institutional study


Anirudh Kulkarni, Dwarakanath Srinivas, Sampath Somanna, Devi Bhagavatula Indira, Chandramouli Bangalore Ananthakrishna 
 Department of Neurosurgery, National Institute of Mental Health and Neurosciences (NIMHANS), Bangalore, India

Correspondence Address:
Dwarakanath Srinivas
Department of Neurosurgery, National Institute of Mental Health and Neurosciences, Bangalore - 560 029
India

Abstract

Objective: The objective was to analyze the demography, clinical presentation, and management of spinal intradural schwannomas in pediatric population. Materials and Methods: This retrospective study includes 21 pediatric patients (under 18 years of age) who underwent surgery for spinal intradural schwannomas from January 1998 to April 2008. The medical records were reviewed retrospectively and the information regarding clinical presentation, tumor location, operative findings, and postoperative status and functional outcome were analyzed. Results: A total of 21 patients (14 females and 7 males) were operated for spinal schwannomas. Six patients had associated neurofibromatosis (five were NF I and one was NF II) at presentation. The most common presenting symptom was progressive myelopathy (86%). The tumor location was either cervical or dorsal in 18 cases. All patients underwent surgery. Gross total excision was achieved in 20 cases. The median follow-up was 38 months. All the patients had neurological improvement in both power and bladder symptoms. Conclusion: Pediatric spinal neurofibromas/schwannomas are an uncommon but completely treatable group of tumors. Complete surgical excision gives excellent outcome.



How to cite this article:
Kulkarni A, Srinivas D, Somanna S, Indira DB, Ananthakrishna CB. Pediatric spinal schwannomas: An institutional study.J Pediatr Neurosci 2012;7:1-3


How to cite this URL:
Kulkarni A, Srinivas D, Somanna S, Indira DB, Ananthakrishna CB. Pediatric spinal schwannomas: An institutional study. J Pediatr Neurosci [serial online] 2012 [cited 2020 Sep 24 ];7:1-3
Available from: http://www.pediatricneurosciences.com/text.asp?2012/7/1/1/97608


Full Text

 Introduction



Tumors of the central nervous system are common in the pediatric population. However spinal tumors constitute only 1-10% of all pediatric central nervous system tumors. [1],[2] Pediatric spinal schwannomas/neurofibromas constitute 2.5-4% of all pediatric spinal tumors. They are firm encapsulated benign tumors and total surgical removal can be achieved in most of the cases with an excellent outcome.

 Materials and Methods



The study included 21 patients in the pediatric age group (<18 years) of spinal schwannomas who underwent surgery over 10 years from January 1998 to April 2008 in the Department of Neurosurgery, National Institute of Mental Health and Neurosciences, Bangalore. Case records of these patients were reviewed retrospectively. The demographic profile, clinical features, radiological findings, operative procedures, postoperative complications, and outcome were noted and analyzed. Follow-up data were analyzed and average duration of follow-up noted.

 Results



Demographic features

There were a total of 21 patients with an age range of 6-18 years with a median age of 16 years. There were 14 females and 7 males (ratio of 2:10).

Clinical features

The duration of symptoms ranged from 1 month to 36 months with average duration of 5 months. The predominant complaint was progressive motor deficits seen in 86% of patients. Localized pain was seen in 67% of patients. Six patients had bladder disturbances (29%) and six patients had associated neurofibromatosis. Among these, five had neurofibromatosis type I with multiple café-au-lait spots and multiple subcutaneous swellings, and one had neurofibromatosis type II with bilateral vestibular schwannomas. One patient had presented with spastic quadriparesis with severe breathing difficulty. This patient underwent emergency decompression of the tumor and was put on ventilator. Gradually the patient was weaned off from the ventilator support and made significant improvement.

Radiology

The predominant location was the cervical region in 10 cases (47%), followed by dorsal in 8 cases (38%). In three patients, the tumor was located in the lumbosacral region. Four of the 21 patients had dumbbell schwannomas.

Management and follow-up

Among the 21 patients, 18 underwent laminectomy, 3 underwent laminotomy and microsurgical excision of the tumor. Twenty patients underwent gross total excision and one underwent partial excision in view of tight adherence to multiple nerve roots in cervical region. Two patients had significant anterolateral extraspinal extension. Hence, they underwent an additional anterior approach and gross total excision. All the patients made gradual improvement in the power. None of the patients deteriorated in power following surgery. One patient had developed wound infection, which was controlled with relevant antibiotics. One patient had developed meningitis that was managed with appropriate antibiotics. Both patients made a gradual improvement.

The follow-up period ranged from 4 months to 56 months with average follow-up period of 38 months. Motor deficits improved by at least one grade in 6 patients and by 2 grades in 10 patients. Two patients had remained status quo in motor power. Of the six patients who had bladder symptoms, four patients made improvement in urinary symptoms and two patients were on intermittent self-catheterization. X-rays of the spine was performed at follow-up and showed no signs of instability in any of the patients. Follow-up MRI at last follow-up revealed no recurrence in any of the patients.

 Discussion



Demography

Spinal schwannomas constitute one third of all primary spinal neoplasms. Spinal cord tumors are a relatively rare diagnosis and account for 1% to 10% of all pediatric central nervous system tumors. This is in contrast with adults where they constitute about 25% of primary intradural tumors. There is no significant prevalence difference between males and females. However, some studies indicate a higher incidence of spinal schwannomas in males, as reported by Hori et al. (60%), Iraci et al. (51%); and Levy et al. (55%). [3] However, a higher incidence in females was reported by Salah et al. (57%), and this percentage corresponds to our study in which 67% of schwannomas appeared in the female population. [3]

Clinico-radiological features

In our study, the majority of the patients presented with progressive compressive myelopathy (86%). The next most common symptom was localized pain (67%). The frequency of motor involvement and localized pain was much higher in our study compared with the available literature where it has ranged from 40% to 60%. The autonomic (bowel and bladder) involvement in our study was 29% compared to 10--20% in the literature. [1] Six patients had associated neurofibromatosis. (Five had NF I and one had NF II.) The most common spinal tumors in NF I are neurofibromas. Paraspinal neurofibromas including dumbbell-shaped tumors are commonly found in asymptomatic patients, especially at younger age groups. Patients with NF II frequently have spinal tumors including intraspinal schwannomas. [4],[5]

In our study the most common location was the cervical region (47%) followed by the dorsal region in 38% of the cases [Figure 1]. This differs from the available literature in which the majority of the tumors are located in the cervical and lumbar regions. [3],[6],[7] According to the available literature 70--80% of spinal schwannomas are intradural in location and those extending through the dural aperture as the dumbbell mass involving both intradural as well as extradural space account for another 15%. [8] Intramedullary schwannomas are extremely rare. [9],[10] In our study, 17 patients had intradural schwannomas (80%) and 4 patients (20%) had dumbbell schwannomas.{Figure 1}

Management strategies

All our patients underwent surgery and excision of the tumor (GTE in 20 and STE in 1); [Figure 2] and [Figure 3] the outcome is comparable to the available literature and correlates with the preoperative neurological status of the patient. {Figure 2}{Figure 3}

 Conclusion



Spinal schwannomas are rare among the pediatric population. Though histologically benign they can produce profound neurological deficits. Microsurgical excision for spinal schwannomas usually results in good postoperative functional outcomes.

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