The clinical data and imaging studies of six patients who suffered with SFT involving the intracranial and extracranial head and neck regions were retrospectively reviewed. These patients were diagnosed during the five-year period from January 1998 to December 2002. The study includes four men and two women, and their mean age was 52 years (age range; 46-59 years). All six patients underwent MR imaging and two patients underwent CT examinations. The MR imaging was performed using a 1.5-T MR unit (Signa; GE Medical Systems, Milwaukee, WI, USA) equipped with a head coil. An axial T1-weighted spin echo sequence (TR/TE/NEX, 466-516/11-14/2; field of view, 18-20 cm; section thickness, 4-5 mm with a 1 mm gap; matrix size, 256 × 256) and an axial T2-weighted spin echo sequence (TR/TE/NEX, 4016-4000/96-104/1; field of view, 18-20 cm; section thickness, 4-5 mm with a 0.4-1 mm gap; matrix size, 256 × 256) were obtained for the precontrast MRI. In addition, contrast-enhanced T1-weighted spin echo images were obtained in the axial, sagittal and coronal planes after the intravenous injection of 0.1 mmol/kg of gadolinium dimeglumine. The CT scan was obtained using a spiral CT scanner (Hispeed; GE Medical System, Milwaukee, WI, USA). The scanning parameters were 120 kVp, 200 mA and a 0.8-sec scan time. Both the unenhanced and enhanced scans were obtained in two patients. One patient underwent only unenhanced CT scanning. The enhanced scans were obtained after the injection of 150 ml of iopromide (Ultravist 300, Schering, Seoul, Korea); 100 ml was injected as a bolus before scanning and 50 ml was infused as a drip during scanning. Contiguous scans with 5-mm collimation were obtained at 5-mm intervals from the external auditory canal to the thoracic inlet for the head and neck imaging, and from the top of the head to the skull base for the brain imaging with the patient performing quiet respiration. The images were reviewed by two radiologists working in consensus, and they were only aware of the histologic diagnosis. Both the CT and MR images were evaluated for the location, margin, contour, MR signal intensity or CT density, internal architecture, pattern of enhancement and the change of the adjacent structure. On the CT and the T1- and T2-weighted MR images, the density and signal intensity abnormalities were categorized as low, iso- or high density/signal intensity as compared with the neck musculature. The margin was graded as well defined or ill-defined, and the contour was graded as smooth or irregular. The pattern of intratumoral enhancement was categorized as homogeneous or heterogeneous, and the degree of enhancement was categorized as strong, moderate or weak. These MR and CT findings were correlated with the microscopic findings of the surgically obtained specimens. Surgical excision was performed in all patients. The histologic evaluation and immunohistochemical studies were performed on the excised specimens. The diagnosis of SFT was established on the basis of the histopathologic appearance and the immunohistochemical pattern of a diffuse and strong positive reaction for CD34. The diagnostic histopathologic findings were the presence of a haphazard growth pattern of short spindle cells having scant cytoplasm and a bland cytologic appearance, and these cells were separated by strands of rope-like collagen (5-8).

The clinical and imaging features of our six patients are given in Table 1. There were two intracranial SFTs and four extracranial SFTs included in this study. The individual locations were the meninges, including the petrous ridge and the pituitary fossa, the parotid gland, the parapharyngeal space, the buccal space and the maxillary sinus. The presenting symptoms were headache in a case of the meninges location, visual disturbance in a case of the pituitary fossa location and an indolent palpable mass in the extracranial located cases. Preoperative diagnosis was meningioma for a case of the petrous ridge location, pituitary adenoma for a case of the pituitary fossa location, pleomorphic adenoma for the cases of the parotid gland and buccal space locations, and neurogenic tumor for the cases with parapharyngeal space and paraspinal area locations. Of the six SFTs, five were well-defined and smooth-contoured, except for one that had an irregular contour. On the MR images, all the SFTs were observed as having iso-signal intensity on the T1-weighted images (Figs. 1D and 3A) and they had high signal intensity on the T2-weighted images (Figs. 1C and 3B), except for a case having a pituitary fossa location, and this tumor had a low signal intensity on the T2-weighted images (Fig. 2B). On the contrast-enhanced T1-weighted images, homogeneous enhancement was observed in four SFTs (Figs. 1E and 3C) and heterogeneous enhancement was observed in two. All six SFTs were strongly enhanced. On the T1- and T2-weighted images, linear or curvilinear low-signal-intensity lines were observed within five tumors, except a case having a pituitary fossa location (Figs. 1C, 1D, 3A, 3B and 4A). These hypointese lines were less enhanced than the other portions of the tumor in four cases (Fig. 3C), and these hypointense lines were enhanced to the same degree as the other portions of the tumor in one case (Fig. 1E).

On the unenhanced CT images, the tumors were observed as having low density in the case of the petrous ridge location (Fig. 1A) and the tumors had a high density in a case of the pituitary fossa location (Fig. 2A). On the contrast-enhanced CT images, heterogeneously strong enhancement was observed in a case having a petrous ridge location (Fig. 1B). Two tumors in the meninges showed adjacent meningeal thickening (a dural 'tail') (Fig. 1E). Adjacent bony erosion was seen in the SFTs having parotid gland and the parapharyngeal space locations due to the large size of the tumors. A SFT of the maxillary sinus expanded into the adjacent nasal cavity and then it was clinically misdiagnosed as angiofibroma. In a case of the tumor with the pituitary fossa location, the tumor displaced the pituitary gland upward.

Microscopic examination revealed benign SFT for all six patients. A more abundant collagenous component and relative hypocellularity were shown in the pituitary SFT of a low signal intensity on the T2-weighted images than was shown for SFTs of a high signal intensity on the T2-weighted images (Figs. 2C and Fig. 3D). The hypocellular, but more collagenous areas in a tumor corresponded to the hypointense lines on the T1- and T2-weighted images.

All patients made uneventful recoveries and they are still clinically and radiologically free from tumor recurrence during the follow-up period that ranged from seven to 27 months (average follow-up period; 13 months).

Solitary fibrous tumor is an uncommon spindle cell tumor that usually occurs in the pleura. The presence of this tumor has also been recently reported in a number of extrapleural sites, including the intracranial and extracranial head and neck regions such as the meninges, orbit, nasal cavity, paranasal sinus, soft palate, epiglottis, thyroid, salivary gland, infratemporal fossa, buccal space and parapharyngeal space (4-8, 11-13). In our study, six SFTs were located, respectively, in the meninges (the petrous ridge and the pituitary fossa), parotid gland, parapharyngeal space, buccal space and the maxillary sinus. The primary SFT of the pituitary fossa in our study is the first one to be reported at this site.

Solitary fibrous tumors occur with equal frequency in both sexes and they usually occur in adults who are aged from 30 to 64 years (6). In our study, the age range was also 46-59 years, but the incidence was higher in men than in women with a sex ratio of 4:2. Clinically, the extrapleural lesions may present with symptoms related to the tumor site or with systemic symptoms such as hypoglycemia, arthralgia, osteoarthropathy or clubbing. These symptoms usually resolve with the tumors' removal (4, 6). Two of our study patients with intracranial SFTs presented with visual disturbance or headache due to the mass effects, and three patients with extracranial SFTs presented with a palpable mass (Table 1). One patient with a maxillary sinus SFT presented with nasal bleeding. None of our study patients experienced systemic symptoms.

Microscopically, the SFTs are well-circumscribed tumors; they are known to have a characteristic patternless arrangement consisting of a varying number of spindle cells randomly arranged in a collagenous background of variable vascularity. Characteristically, there are alternating hypercelluar and sclerotic hypocellular regions. Some cases have a hemangiopericytoma-like pattern of irregular branching vessels and occasionally a storiform or herringbone pattern is seen (5-8, 12, 13). The SFT diagnosis is supported by a characteristic immunohistochemical profile. SFTs strongly stain for CD34 and the intermediate filament vimentin, but they are usually negative for epithelial, vascular, neural crest and muscle markers (5-8, 13).

According to the reported MR features of SFTs, the signal intensity was isointense to muscle on the T1-weighted images, the signal intensity increased with intravenous gadolinium and it was variable on the T2-weighted images. It's been suggested that this variable signal intensity depends mainly on the differences in the main components of the tumor, namely, the amount of collagen and fibroblasts, and also on the presence of degeneration. Intense enhancement of an SFT is generally due to its high vascularity (8, 15). Several MR studies that were done on fibrosis reported that mature fibrous tissue usually has a low signal intensity on the T1-weighted, proton-density-weighted and T2-weighted images, and this is related to the areas of hypocellularity and the abundant collagen stroma (9, 10). In our study, the tumor signal intensity on the T2-weighted images decreased as the collagenous component increased (Figs. 2B, 2C, 3B and 3D). We also observed an interesting finding, that is, the linear or curvilinear hypointense lines within the tumors on the MR images in four cases (Figs. 1C, 1D and 3A). Those lines corresponded to the hypocellular collagenous stroma intervening in the hypercelluar area, and this hypocellular collagenous stroma was composed of a haphazard proliferation of spindle cells. Even if these hypointense lines were not specific for SFT, we suggest that these hypointense lines are helpful for including this rare tumor in the differential diagnosis of masses involving the intracranial and extracranial head and neck regions.

For the CT-pathologic correlation of nine cases having a pleural origin, Lee et al. (14) described these tumors as having isoattenuation relative to the adjacent musculature, and they had intense enhancement following intravenous contrast injection. The intratumoral low attenuation areas correlated with myxoid or cystic degeneration. In our study, an SFT located in the pituitary fossa was hyperdense on the unenhanced CT images. We presume that the compactly arranged, abundant, collagenous component of this tumor increased the density of the tumor on the CT images, and this was seen as a decreased signal on the T2-weighted MR images.

Most intracranial SFTs have a dural origin, and although there have been several reports of intracranial and spinal meningeal SFTs (8, 11), an SFT in the pituitary region has never been reported on before. Thickened dural 'tails', hyperostosis, skull erosion and capping cysts may all be seen in meningeal SFTs (8). The two meningeal SFTs in our study were also shown to have dural tails.

The radiologic appearance for SFTs of the intracranial and extracranial head and neck regions is nonspecific, and this tumor is often misdiagnosed as being another type of common tumor on the initial images. In our case of the pituitary SFT, the tumor was initially considered to be a pituitary adenoma with hemorrhage because of its low signal intensity on the T2-weighted images. A transsphenoidal approach for resection of this tumor resulted in its incomplete excision because of the harder consistency of the SFT. This patient had to undergo repeated surgery using a transcranial approach in order to achieve complete tumor resection. Therefore, any suggestion of the characteristics of this hard, fibrous tumor, according to its MR signal intensity, may be important for the subsequent patient care.

Most SFTs, especially those in the extrapleural sites, are benign and they are cured with complete surgical excision. Previous reports have indicated that 13-37% of SFTs have been associated with local recurrence or histologic malignancy such as an invasive growth pattern, cellular pleomorphism, abundant mitotic activity or metastasis (5-8, 10, 16). There is no report that a benign SFT has a potential to transform into a malignant SFT.

Solitary fibrous tumor is an uncommon tumor occurring in the intracranial and extracranial head and neck regions. On the MR images, this tumor is seen as a well-defined, smooth or irregular, contoured mass. It is isointense relative to muscle on the T1-weighted images; the intensity increasing with intravenous gadolinium, and the intensity is variable on the T2-weighted images. Darker signal intensity on the T2-weighted images represents a firmer fibrous tumor composed of abundant collageneous stroma. Solitary fibrous tumor should be included in the differential diagnosis of masses involving the intracranial and extracranial head and neck regions because it has imaging findings similar to those of the other more common lesions such as schwannoma and meningioma.