A 22-year-old woman was admitted to the outpatient department with a 1-month history of left leg weakness and hypesthesia below the T2 level. Magnetic resonance (MR) images showed a 2.2×1.3 cm tumor at T1-2 (Fig. 1). The margin of the tumor was well defined, and the neural foramen was widened by the tumor, suggestive of a slow-growing tumor. The tumor showed broad isointensity with respect to the spinal cord on T1- and T2-weighted MR images and demonstrated homogeneous enhancement of the tumor on T1-weighted images. The tumor demonstrated an unusual pattern of internal low signal speckled dots on T1 enhanced MR images (Fig. 1E).

The patient underwent T1-2 laminoplastic laminotomy, and the tumor was exposed. The tumor looked similar to a typical schwannoma, appearing pearly yellow and white, with eccentric attachment to a nerve root. Although the tumor was friable, its capsule was tough and adhered tightly to the root. The two roots adhering to the capsule were sacrificed. At the completion of the resection, there was no change in the electrophysiological monitoring. On the histological exam, the tumor cell had abundant cytoplasm with eosinophilic granules (Fig. 2). Immunohistochemical analysis showed the tumor cells were strongly and diffusely immunoreactive with S-100 protein and CD68. The patient's hypesthesia improved after surgery. Follow-up MR imaging performed 12 months after surgery showed no evidence of recurrence.

A 21-year-old woman presented with a 3-month history of right arm pain and tingling. The sensory changes had been present for 10 years, but she had not received any treatment. Her symptoms were aggravated after a minor car accident. She had no relevant medical or family history. Physical examination revealed intact motor power and normal reflexes. Computed tomography (CT) showed bony erosion at the right C5 and C6 foramina, and the right vertebral artery was displaced anteriorly. MR images demonstrated a 3.5×2.3 cm dumbbell-shaped IDEM mass at C5-6 that extended to the right extraforaminal space. The tumor showed isointensity with respect to the spinal cord on T1-weighted images and homogeneous gadolinium-enhanced T1-weighted images (Fig. 3). Speckled dots were also observed on the T2-weighed images and gadolinium enhanced T1-weighed images. As in Case 1, the tumor showed low signal speckled dots especially on the T1 enhanced images. Complete tumor resection was performed. The histological findings showed lymphocytic infiltration around granular cells (Fig. 2). The tumor cells were strongly immunoreactive with S-100 protein on the immunohistochemical analysis. The postoperative course was uneventful, and the patient experienced significant relief of her tingling sensation.

Our two GrCTs showed speckled dots in the tumor characterized by low signal dots, especially on enhanced T1-weighed images. We reviewed all of the published literature on GrCTs and found that the majority of published cases that included MR images also revealed this feature (Table 1). We have not observed such a pattern in other similar tumors, such as schwannoma and meningioma, nor has it been reported. Based on these results, speckled dots potentially are a characteristic for the differential diagnosis of GrCT.

The physical reason behind the low signal speckled dots may be hyalinizing fibrosis of GrCTs. By histology, GrCTs consist of clusters and sheets of large rounded, polygonal or elongated cells with indistinct cellular borders. The tumor clusters consist of small, hyperchromatic to vesicular nuclei and background fibrous connective tissue. The islands of the tumors are separated by delicate fibrovascular tissue12). Case 1 showed fibrosis and vacuole changes, and Case 2 demonstrated hyalinizing fibrosis and lymphocytic infiltration. Other reported cases are summarized in Table 2. Fibrosis of GrCT is well described in 6 of 8 patients. The other 2 cases did not show fibrosis, but this was uncertain. Previous researchers have reported that GrCTs in the appendix and skin also demonstrate a telangiectatic portion with a fibrotic or hyalinized wall, stromal area and lymphoid infiltration7). Fibrosis may be a common factor correlating with the low signal intensities in MR. Therefore, speckled dots may be observed in GrCT as a result of the fibrosis.

It is believed that GrCT arises from Schwann cells1). This is supported by positive reactions to various neural markers, including S-100 protein, neuron-specific enolase, and inhibin-alpha3). One of our cases had a dumbbell-shaped tumor that appeared to have an intradural extramedullary origin, possibly from a spinal root. Both GrCT and schwannoma tended to occur more frequently at thoracolumbar junctions. These features would seem to indicate a close relation between GrCT and schwannoma. On the other hand, GrCTs can show malignant characteristics : rapid growth, large size, necrosis, and the involvement of adjacent tissue3,6). In addition, up to 7% of both malignant and benign cases recur after incomplete resection4). Although it has been proposed that radiation therapy successfully stabilizes recurrent disease in intradural extramedullary tumors12), complete surgical resection is recommended as the initial treatment of choice. If a significant morbidity rate is anticipated, as with spinal cord tumors, adjuvant radiotherapy after tumorectomy may lead to better outcomes.