Epibulbar schwannoma in a 12-year-old boy: A case report and review of literature

Indian J Ophthalmol. 2015 Jul;63(7):620-2. doi: 10.4103/0301-4738.167106.

Abstract

Schwannomas are benign, encapsulated, primary neurilemmal tumors composed of proliferating Schwann cells. Schwannomas are commonly seen in the orbit, but are rare on the epibulbar surface. Herein, we report a case of a 12-year-old boy who presented to us with a slow-growing painless subconjunctival mass in the left eye. There was no intraocular extension of the mass and intra-operatively, the mass could be clearly delineated and was excised off the underlying sclera. Histopathological examination of the mass showed typical features of schwannoma and immunohistochemistry helped to confirm the diagnosis. There was no recurrence of the lesion observed at follow-up 26 months after surgery. Here, we describe this uncommon tumor and review the available literature. Although rare, an epibulbar schwannoma should be considered in the differential diagnosis of an amelanotic, painless subconjunctival nodular mass. Excision of the lesion is the recommended treatment.

Publication types

  • Case Reports
  • Review

MeSH terms

  • Child
  • Conjunctiva / pathology*
  • Conjunctival Neoplasms / diagnosis*
  • Conjunctival Neoplasms / surgery
  • Diagnosis, Differential
  • Follow-Up Studies
  • Humans
  • Male
  • Neurilemmoma / diagnosis*
  • Neurilemmoma / surgery
  • Ophthalmologic Surgical Procedures