Introduction
Subependymoma is a rare central nervous system neoplasm that is classified as a grade I tumor by the World Health Organization (WHO) [
1‐
4]. It is of subependymal origin and represents approximately 0.2–0.7% of all intracranial tumors [
2,
5‐
7]. The first pathological description of subependymoma was reported in 1945, with few clinical studies reported since then [
1,
8,
9]. These lesions are typically discovered incidentally and are usually asymptomatic [
10].
Subependymomas are most commonly found in the fourth and lateral ventricles; however, a number of studies have reported lesions located in the spinal cord [
3,
11‐
13]. Histologically, they appear as clusters of isomorphic nuclei embedded in a dense glial fibrillary matrix. Symptomatic lesions most frequently present with hydrocephalus and headache. Surgery is considered the primary treatment option for symptomatic cases [
9,
14,
15]. There is a paucity in the literature regarding the imaging characteristics of these rare tumors. Here, we describe the clinical and radiological characteristics of 29 patients with fourth ventricle subependymoma as observed in two tertiary care academic medical centers.
Methods
Study design
This retrospective case series was performed after Institutional Review Board (IRB) approval at two participating institutions. Patients with intracranial subependymoma were identified via a database search at the University of Texas M.D. Anderson Cancer Center and the University of Texas Southwestern Medical Center. Patients 18 years of age or older diagnosed with fourth ventricle subependymoma via magnetic resonance imaging (MRI) or histopathology from 1993 to 2019 were included in the study.
Exclusion criteria consisted of patients younger than 18 years of age, subependymoma located outside the fourth ventricle, or absence of MRI images. A retrospective review of clinical, radiological (MRI), and pathological data was performed. MRI appearance was used to make the diagnosis of subependymoma in cases where surgical pathology was unavailable. All MRI images were reviewed by 3 fellowship-trained, board certified neuroradiologists with greater than 4 years of experience.
Study variables
Patient demographic and imaging variables such as age, gender, date of initial MRI, date of last MRI, date of surgery, and symptoms at diagnosis were collected. Specific imaging variables for each patient collected included tumor location, tumor size, degree of enhancement, intensity of enhancement, appearance on T1, T2, FLAIR, DWI, GRE, and any change in imaging. The degree of enhancement was further characterized as non-enhancing, partially enhancing, and completely enhancing. The intensity of enhancement was further characterized based on the highest degree of enhancement into 3 categories: avid, moderate, and mild. Avid enhancement was defined as enhancement intensity similar to homogeneous dural venous sinus enhancement without flow artifacts. Moderate enhancement was defined as enhancement intensity similar to the degrees of enhancement of the choroid plexus. Mild enhancement was defined as enhancement intensity less than that of the choroid plexus. The change in imaging was defined as a minimum 25% increase in baseline tumor size for patients managed conservatively, while for patients treated via surgery, the change in imaging was defined as tumor recurrence.
Statistical analysis
Tumor volume was calculated as [Anteroposterior × Transverse × Craniocaudal]. Analysis for descriptive statistics was performed using the statistical software SPSS V.24 (IBM Corp., Armonk, New York).
Discussion
In this study, we report the largest imaging experience to date on 4th ventricular subependymoma. The majority of patients in this study were confirmed histopathologically as subependymomas. Also included were adult patients with tumors of the 4th ventricle that exhibited imaging stability over time in keeping with low-grade neoplasm, thus excluding other known pathologic entities of the 4th ventricle known to be progressive lesions such as ependymoma or medulloblastoma [
21‐
25]. This strategy also excluded 4th ventricular tumors that although low-grade are known to be symptomatic requiring surgery such as choroid plexus papillomas or pilocytic astrocytoma and known to have an aggressive course when presenting in adulthood [
22‐
28]. Furthermore, the MR imaging characteristics appeared relatively uniform between the operative and non-operative cohort, supporting a common pathology.
Our study is the first to identify a specific site of origin for 4th ventricular subependymomas. All patients in our cohort were found to have tumors originating below the body of the 4th ventricle and above the obex. This observation in conjunction with long-term imaging stability suggests the likely diagnosis for these rare tumors. Furthermore, the presence of tumor at the foramen of Luschka or Magendie as well as larger tumor size was observed to be linked with clinical symptoms requiring surgical resection. This is in contrast to the patients that were placed on imaging surveillance where no patients exhibited symptoms, only one patient had tumor at the foramen of Luschka, and tumors were noted to be smaller in size compared to the operative cohort.
As noted in the literature, intracranial subependymomas are most commonly found in the fourth and lateral ventricles [
10,
16‐
18]. Within the fourth ventricle, we observed all of the subependymomas in our study to be centered below the body of the fourth ventricle and terminating at the level of the obex. We postulate that this neuroanatomical finding may have a developmental relationship with the area postrema, a circumventricular paired structure in the medulla oblongata of the brainstem [
19]. The area postrema is located at the floor of the fourth ventricle, highly vascular, and lined by glial cells. The cell of origin for subependymomas is thought to originate from neural stem cells. Bennett et al. have suggested that circumventricular organs such as the area postrema may be a novel source of neural stem cells, raising the developmental concept of subependymomas originating in this area [
20]. Obviously, this hypothesis requires further investigation.
Radiographic findings in our study revealed that fourth ventricle subependymomas are more commonly isointense on T1, hyperintense on T2, enhance, and demonstrate FLAIR hyperintensity. The presence of susceptibility artifact was seen in 75% of our patients and was found to represent coarse calcification on CT in a limited number of patients that had CT available for comparison. Though the majority of cases in our study demonstrated enhancement, it is worth noting that most of these tumors exhibited relatively mild to moderate enhancement. This is generally consistent with what has been previously described in multiple retrospective case series with regards to intracranial subependymoma [
8,
10‐
12,
16‐
18,
21,
22]. It is worth noting that none of our lesions demonstrated complete enhancement, and only one demonstrated avid enhancement. This may be helpful when differentiating from lesions with characteristic complete or avid enhancement, such as papillomas, meningiomas, and hemangioblastomas [
23‐
28].
Nearly half of the cases in our study demonstrated tumor extension outside of the fourth ventricle, either into foramen of Magendie or Luschka. Though sparingly noted in the literature, no studies have drawn any correlation between subependymoma extension outside of the fourth ventricle and diagnosis [
18]. However, we observed that the larger tumors in our study appeared to have a greater incidence of extension outside of the fourth ventricle.
There was an appreciable difference in tumor size between the operative and non-operative cohorts in our series, with the operative tumor cohort being consistently larger in size than the non-operative cohort. All symptomatic lesions in our study underwent surgical resection. The most common symptoms noted in our study included headache and dizziness, which are consistent with the literature [
10,
14,
22,
29]. Obstructive hydrocephalus was also observed in three of our patients before surgery, which was noted in the literature to be a particular sequelae of fourth ventricle subependymoma [
10,
17,
18]. None of the cases in our study experienced tumor recurrence, consistent with the literature regarding the clinical management and cellular growth of intracranial subependymoma [
8,
9,
12‐
15,
30].
Our study is a retrospective case series pooling data from two large tertiary academic medical centers. It has several limitations, including inherent bias due to the retrospective and observational nature of the study. A possible geographic bias regarding patient demographics can also limit our study due to both participating institutions being in the same region, while patient insurance status can also possibly bias the patient cohort that was available for our study. Our small sample size may be biased toward larger or more symptomatic lesions, since asymptomatic lesions are less likely to present and undergo imaging. Also, our cohort consists of only 18 patients with a histologically confirmed diagnosis. Our length of follow-up is relatively short; however, it is understood that these are benign tumors. Furthermore, a larger study would be difficult to perform for such rare and indolent tumors.
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