Extraventricular neurocytoma in the left temporal lobe: A case report and review of the literature

Introduction

Central neurocytomas (CNCs) are rare brain tumors that originate from neuroepithelial tissue, occurring most frequently in young adults, and are often located in the lateral ventricles. CNC was first described by Hassoun et al (1) in 1982, and accounts for 0.1–0.5% of all primary brain tumors (2). Complete surgical resection is currently the optimal treatment choice, and the prognosis of CNC is often favorable due to its benign nature (3). Although CNC typically occurs in the lateral ventricles, a few cases of CNC occurring in extraventricular regions have been reported in the literature.

Case report

In March 2014, a 49-year-old man was admitted to the Tsinghua University Yuquan Hospital (Beijing, China) after experiencing headaches for 3 weeks. No other focal neurological deficits were observed upon admission. Computed tomography (CT; SOMATOM Sensation 16; Siemens AG, Munich, Germany) of the brain identified an isodense, round, well-demarcated, 3.3-cm tumor, which was located in the left temporal lobe, in addition to peritumoral edema (Fig. 1A). Marked homogeneous enhancement was observed within the mass on T1-gadolinium imaging (Fig. 1B). The patient underwent surgery, and the tumor was excised via a left temporal craniotomy. As there was no adhesion between the tumor and the dura or the brain, the radical resection of the lesion was straightforward. The pathological report stated that the tumor was a grade II extraventricular neurocytoma (EVN) according to the World Health Organization (WHO) classification of tumors of the central nervous system (4). Resected tissue specimens were formalin (Yuekai Trading Co., Ltd., Hebei, China)-fixed, paraffin (Sinopharm Chemical Reagent Co., Ltd., Shanghai, China)-embedded, cut into 8-µm sections, stained with hematoxylin and eosin (Shanghai Qianchen Biotechnologies, Co., Ltd., Shanghai, China) and visualized using an optical microscope (CX23; Olympus Corporation, Tokyo, Japan). Histologically, the resected tumor tissue contained clusters of small cells with regular nuclear morphology, and round nuclei with fine chromatin (Fig. 2). Vascular hyperplasia was also observed. There was no evidence of ischemic necrosis or hemorrhage. For immunohistochemical staining, tissue sections were incubated with monoclonal mouse anti-rat synaptophysin (cat. no. ab11105; 1:500; Abcam, Cambridge, MA, USA), rabbit anti-mouse neuronal nuclear antigen (cat. no. ab190565; 1:50; Abcam) and mouse anti-human Ki67 (cat. no. ab8191; 1:50; Abcam) antibodies overnight at 4°C. The sections were then washed with PBS, incubated with biotinylated goat anti-mouse (cat. no. ab97233; 1:300; Abcam) or goat anti-rabbit (cat. no. ab97188; 1:300; Abcam) secondary antibodies for 30 min and staining was visualized using an optical microscope (CX23; Olympus Corporation). Immunohistochemical staining revealed that the tumor cells expressed the neuronal differentiation markers, synaptophysin and neuronal nuclear antigen (Fig. 3). Ki-67, a marker for proliferation index, was detected in 10% of the tumor nuclei. The patient was discharged from hospital without further treatment, including radiotherapy or chemotherapy. The patient was followed up for 3 months post-surgery, with magnetic resonance imaging (MRI; Signa HDe 1.5T; GE Healthcare Bio-Sciences, Pittsburgh, PA, USA) of the brain demonstrating no evidence of tumor recurrence (Fig. 1C). After the initial 3 month follow-up period, the patient was followed-up every 6 months, and at the time of writing no recurrence had been identified.

Figure 1. Pre- and post-surgery brain scans of the present case. (A) CT revealing a isodense, well-demarcated, round tumor located in the left temporal lobe, in addition to peritumoral edema. (B) T1-gadolinium image revealing a homogeneously-enhanced mass. (C) Post-operative magnetic resonance imaging demonstrating no signs of solid tumor recurrence. CT, computed tomography.

Figure 2. Histological analysis of the resected tissue exhibiting clusters of small cells with regular nuclear morphology and round nuclei. Staining, hematoxylin and eosin; magnification, ×100.

Figure 3. Immunohistochemical staining revealing expression of (A) synaptophysin and (B) neuronal nuclear antigen in the tumor cells. Magnification, ×100.

Discussion

CNC is most prevalent in adolescents and young adults, and is often located in the lateral ventricles. In 1997, Giangaspero et al (5) reported the first case of a tumor that mimicked CNC, but was located in an extraventricular region. In 2007, these tumors were classified by the WHO as a novel brain tumor entity (4), and the incidence of EVN remains extremely rare, with Liu et al (6) reporting a worldwide incidence of only 0.13%. The development of CNC appears to have no significant gender predilection; however, the literature indicates that EVN has a slight female predominance and a median patient age of 38 years (range, 5–76 years) (7,8).

Increased intracranial pressure is the most common clinical presentation, particularly for CNC of the lateral ventricles. Other symptoms may vary from seizure to gait disturbances depending on the tumor location. The most frequent symptom of EVN is complex partial seizure, followed by headaches, precocious puberty, cranial nerve paralysis, and on rare occasions, hemorrhage (9). Various other non-specific symptoms are also associated with the disease, including headache, dizziness, weakness, and memory and consciousness dysfunction (10). A large number of patients present with these non-specific symptoms, and thus there are no definitive symptoms to diagnose EVN.

EVNs do not present with specific imaging characteristics. On imaging analysis, EVNs may appear as well-circumscribed, round or multilobular, hypodense or isodense masses, which are homogeneously-enhanced with contrast medium, as observed in the present case. Liu et al (6) reported that cystic degeneration was observed in 6 out of 9 (66%) EVN cases, with calcification in 34% and perilesional edema in 44%, whilst Patil et al (11) reported that cystic degeneration was present in 71% of 9 cases and perifocal edema in 57%. MRI may exhibit an isointense or slightly hyperintense signal compared with the cortex on T1- and T2-weighted images. The majority of EVN tumors are solid, but largely cystic masses, and mural nodules may be identified. Moderate enhancement is typically observed in these tumors, however, following administration of a contrast agent, mild to strong heterogeneous enhancement may be exhibited (12–14). Common differential diagnoses include oligodendroglioma, ependymoma and dysembryoplastic neuroepithelial tumors, all of which usually lack a clear margin. Contrast enhancement and cystic changes also assist in distinguishing EVNs from other lesions. MR spectroscopy studies of EVNs have demonstrated a prominent choline peak with a notably decreased or absent N-acetylaspartate peak when compared with intraventricular neurocytomas (15).

A characteristic histological feature of EVNs is their composition of monotonous neoplastic cells with round, regular nuclei embedded in a matrix of fine neuronal processes, known as a neuropils. These neuropils are much finer than glial processes and exhibit a ‘velvety’ appearance, assisting their differentiation from typical rosettes observed in an ependymoma (16). Atypical EVNs are characterized immunohistochemically by a Ki-67 index of >2%, or by atypical histological features, including increased mitotic activity, focal necrosis and vascular proliferation (17). Histologically, EVN may also resemble oligodendroglioma, therefore, immunochemistry is required to a make an accurate diagnosis. Oligodendrogliomas may exhibit a limited amount of synaptophysin positivity in the tumor cell cytoplasm, but not to the same degree or extent as EVNs (18,19). EVNs may also occasionally carry the 1p19q codeletion, which is observed in 50–80% of oligodendroglioma cases (19).

Complete surgical excision is currently considered as the optimal treatment for EVN, but is often limited by tumor proximity to eloquent areas (20). In cases of incomplete resection, available data suggests that radiotherapy offers the same tumor control rates for EVN (11). The success rate of Gamma Knife® radiosurgery has not yet been discussed in the literature due to the limited number of EVN cases.

Post-operative radiation therapy may be effective in reducing tumor size and recurrence rates in cases of aggressive atypical neurocytoma; the recommended dose of 50 Gy is considered to be the most appropriate for long-term local control in children (20). Additional Gamma Knife stereotactic radiosurgery may be performed post-surgery in order to obtain improved local control and a higher survival rate for cases that cannot be surgically resected (7). The potential benefits of chemotherapy for recurrent tumors and residual lesions is uncertain and is not currently supported in the literature.

In the present case, complete surgical resection was performed due to the clear boundary of the tumor. Further treatment was not necessary, and the patient was followed-up 3 months post-surgery, with MRI of the brain indicating no signs of recurrence.

EVNs are benign in nature, with the exception of aggressive atypical variants (21). There is no association between tumor recurrence and tumor location, and pathology is one important prognostic factor. Atypical EVNs are characterized by a Ki-67 proliferation index of >2% or by atypical histological features, including vascular proliferation, focal necrosis and increased mitotic activity. As a result of these features, atypical EVN is difficult to resect completely. Kane et al (22) reported that a typical EVN histology significantly predicts a poor outcome with higher recurrence and mortality rates. Age is an additional prognostic factor, with an age of >50 years serving as a risk factor for recurrence, and an age of <18 years often associated with atypical features (16).

In conclusion, EVN is extremely rare and presents with varying clinical symptoms and imaging characteristics. The current case described a 49-year-old patient with EVN and discussed the associated clinical presentation, radiological manifestation and histopathological features. Total surgical resection of the tumor was considered as the optimal treatment. However, post-operative radiation therapy may be an effective therapeutic supplement for cases of incomplete resection. In addition, long-term follow-up is essential for cases of atypical EVN.

References