Introduction

Solitary fibrous tumors (SFTs) were originally described in pleura and subsequently in soft tissue and many other organs including the central nervous system. SFTs of the central nervous system are rare entities, usually presenting as dura-based masses predominantly in the posterior fossa and spinal region [1]. SFTs are composed of spindle cells in a collagenized stroma with characteristic immunohistochemical features: diffuse and strong reactivity to CD34, positive for vimentin, and often immunoreactive to CD99 and Bcl-2 [1]. Intra-ventricular SFTs are rare, and only six cases have been reported in the fourth ventricle [2–7].

Case presentation

Our patient was a 52-year-old African-American man who presented to our facility with a two-month history of progressive weakness and numbness in all extremities. A computed tomography (CT) scan and a brain magnetic resonance imaging (MRI) scan revealed a 4.5 × 3.7 × 2.7cm, homogeneous, avidly enhancing mass located in the fourth ventricle, compressing adjacent medulla and cerebellum and extending into the foramen of Luschka (Figure 1). Angiography demonstrated multiple dysplastic-appearing branches from the right posterior inferior cerebellar artery supplying the neoplasm.

Figure 1
figure 1

Contrast-enhanced T1-weighted axial (A) and sagittal (B) magnetic resonance imaging scans showing a homogenous mass located in the fourth ventricle.

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Our patient underwent a suboccipital craniotomy and resection of the tumor. During the operation, a cavitron ultrasonic surgical aspirator as well as bipolar cautery and suction were used to debulk the tumor, followed by a combination of RHOTON™ dissectors as well as microscissors to separate the tumor. The entire tumor was successfully removed.

Histological examination showed a spindle cell neoplasm with prominent collagenized stroma (Figure 2A). Mitotic figures were not readily found and the molecular immunology Borstel-1 (MIB-1) proliferation index was low (1%). Meningothelial whorls and psammoma bodies were absent. The neoplastic cells were strongly and diffusely positive for CD34 (Figure 2B), vimentin and Bcl-2 (Figure 3A); no immunoreactivity with S-100, CD99 and epithelial membrane antigen (EMA) was detected. A CD31 immunostain highlighted the endothelial cells but not the spindle tumor cells. A moderate reticulin network was demonstrated by reticulin staining, but individual cells were not invested by reticulin fibers (Figure 3B). The histological features and immunoprofile were consistent with SFT.

Figure 2
figure 2

Photomicrographs (original magnification, 200×). (A) Bland spindle cell tumor with collagenized stroma. (B) Neoplastic cells are strongly immunoreactive to CD34.

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Figure 3
figure 3

Photomicrographs (original magnification, 200×). (A) The tumor cells are immunoreactive to Bcl-2. (B) Neoplastic cells have moderately rich reticulin network.

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Our patient experienced no neurological deficit after surgery, and there were no signs of recurrence at one-year follow-up.

Discussion

Intraventricular tumors can have a wide spectrum of differential diagnosis based on radiological and histopathological features. A bland spindle cell tumor with collagenized stroma and avid contrast enhancement initially suggested a diagnosis of fibroblastic meningioma. However the immunoprofile of the neoplastic cells was typical of a solitary fibrous tumor (negative for EMA, strongly positive for CD34, vimentin and Bcl-2). In contrast, meningiomas are EMA positive and CD34 negative. Hemangiopericytomas can have histological overlap with solitary fibrous tumor, but CD34 and Bcl-2 staining is weak and patchy [8].

To the best of our knowledge, just 17 Intraventricular solitary fibrous tumors have been reported in the literature to date. Six of these tumors were located in the fourth ventricle [2–7], eight cases were in lateral ventricle location [1, 9–14], one tumor located in the third ventricle [15], one case occurred in the foramina of Monro [16] and one case was a recurrent SFT arising from the falx cerebri, extending to the bilateral lateral ventricles and the third ventricle [17]. The clinical and radiological features of these tumors are given in Table 1; the immunomorphological features are given in Table 2. The age of patients ranged from 11 to 75 years old, with the vast majority being over 40 years; there was no sex predominance. Based on the available data, all the tumors were less or equal to 5.0 cm in their greatest dimension. On MRI scans, the tumors are typically iso- to hypointense on T1-weighted images, and show intense and homogeneous enhancement after intravenous administration of gadolinium. Most of those SFTs had bland histological features except two tumors showed mild to marked pleomorphism [5, 11]. Intraventricular SFTs have an indolent clinical course and excellent prognosis after surgery; however, owing to the small number of cases and limited follow-up, more data is needed to better assess the biological behavior of these tumors and the long-term outcome after treatment.

Table 1 Summary of clinical and radiological features of intraventricular solitary fibrous tumors reported in the literature
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Table 2 Summary of immunomorphological features of intraventricular solitary fibrous tumors reported in the literature
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Conclusions

We report a rare case of SFT in an unusual location. Though rare, SFTs should be considered in the histological differential diagnosis of intra-ventricular tumors particularly, spindle cell tumors with collagenized stroma, along with meningioma and schwannoma.

Consent

Written informed consent was obtained from the patient for publication of this manuscript and any accompanying images. A copy of the written consent is available for review by the Editor-in-Chief of this journal.