INTRODUCTION-
Solitary fibrous tumour is a spindle cell neoplasm that commonly arise in the pleura and other serosal regions with more than 50% of these tumours located in the thoracic cavity, however extrathoracic tumours have been reported in various sites such as the liver, skin and the head and neck. Solitary fibrous tumours (SFTs) of the head and neck region are extremely rare with oral cavity being the most common site
MATERIALS AND METHODS-
A 60 yr. old lady presented with a painless right submandibular swelling that had increased in size during the previous 8 months with no constitutional symptoms. Clinically, there was a firm, mobile,6x5 cm right submandibular swelling with no palpable cervical lymph nodes, calculi and the submandibular duct opening was patent. MRI showed a well-defined heterogeneously enhancing lesion involving the right submandibular gland likely neoplastic. FNAC and USG guided core needle biopsy failed to yield any conclusive results. The patient then underwent complete removal of the tumour.
RESULTS-
Since SFT are rare and share many histological features with other spindle cell neoplasms of the salivary gland, immunohistochemistry is an essential tool to correctly diagnose SFT. NAB2-STAT6 gene fusion product is a highly sensitive and specific marker for SFT and is considered the molecular hallmark. In our case, the resection specimen showed the characteristic histopathological findings for SFT and stained positive for STAT6, CD34, CD99, and BCL-2.
CONCLUSION-
Clinicians should include SFT in the differential diagnosis of tumours that arise from soft tissues of the head and neck. Immunohistochemical staining is essential to diagnose SFT. Management is complete excision of the mass with long term follow up, because of the potential for recurrence and malignant transformation.