Sublingual Schwannoma: A Rare Case Report with Diagnostic and Surgical Challenges

Ankita Singh, Kaustubh Mehta, Mayur Kothiya, Ram Singh
Author(s)
1GDMO, Department of ENT, Rajawadi Hospital, Mumbai, India. 2SMO, Department of ENT, Rajawadi Hospital, Mumbai, India. 3SMO, Department of Pathology, Tata Memorial Hospital, Mumbai, India. 4Registrar MW Desai Hospital, Mumbai, India

Abstract

Background: Schwannomas are solitary, slow-growing, benign tumors made of nerve sheath Schwann cells. Oral cavity involvement is rare, although around a quarter occur in the head and neck region. The patient in this publication is a 32-year-old woman who has a distinct, painless, slowly increasing swelling in her left sublingual area. Clinical presentation, FNAC, and contrast-enhanced CT were inconclusive. Complete surgical excision with enucleation and primary closure was performed. Definitive diagnosis was made by histology (Antoni A and B areas, Verocay bodies) and immunohistochemistry (S-100 positivity). The patient recovered uneventfully with no recurrence. Sublingual schwannoma, though rare, should be considered in differential diagnosis of floor-of-mouth swellings.

Keywords: Schwannoma, sublingual space, oral cavity, S-100, enucleation.


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