J Rhinol.  2024 Nov;31(3):184-188. 10.18787/jr.2024.00028.

Vidian Nerve Schwannoma Extending Into the Foramen Rotundum in a Female Patient: A Case Report

Affiliations
  • 1Department of Otorhinolaryngology-Head and Neck Surgery, Kyung Hee University Hospital at Gangdong, Kyung Hee University College of Medicine, Seoul, Republic of Korea

Abstract

Schwannomas are benign tumors that can develop in any part of a nerve containing Schwann cells. Skull base schwannomas are rare, representing approximately 4% of extracranial schwannomas. Among these, vidian nerve schwannomas are particularly uncommon, with only a few documented cases. In this report, we describe the case of a 58-year-old female patient who presented with an incidental finding of a skull base mass. The patient’s only symptoms were intermittent headaches and dry eyes. No mass was detected during the physical examination. Radiographic evaluation revealed a neoplasm within the vidian canal, and the lesion’s characteristics suggested a schwannoma. The patient underwent endoscopic resection, and subsequent histopathological analysis confirmed the diagnosis of schwannoma. Follow-up imaging and physical examination showed no evidence of recurrence. This case report highlights a schwannoma located in the vidian canal and extending into the foramen rotundum, which was successfully managed with endoscopic surgery.

Keyword

Neurilemmoma; Nerve sheath neoplasms; Transnasal endoscopic surgery; Foramen rotundum

Figure

  • Fig. 1. Axial and coronal views of a computed tomography scan of the paranasal sinus. A: A round mass is observed within the vidian canal, extending into the left sphenoid sinus. The pterygopalatine fossa remains intact. B: A soft tissue density mass-like lesion (asterisk) occupies the vidian canal, extending into the sphenoid sinus and foramen rotundum. The medial wall of the foramen rotundum’s bony canal is partially eroded. White arrowhead: right vidian canal. Black arrowhead: right foramen rotundum. White arrow: left foramen rotundum, showing destruction of the bony canal.

  • Fig. 2. Preoperative axial and coronal magnetic resonance image. A: A hypermetabolic lesion exhibiting a heterogeneously enhanced “salt and pepper” sign is observed on a T1-weighted axial image. B: The left maxillary nerve is not observed on the T1-weighted coronal image, in contrast to the foramen rotundum on the right side (white arrowhead).

  • Fig. 3. Intraoperative image of schwannoma. A: A round mass containing yellowish tissue (asterisk) is visible. Intracapsular piecemeal resection was performed using the appropriate equipment. B: All intracapsular components were removed and confirmed with a 30° endoscope.

  • Fig. 4. Histopathologic findings of the mass. A: Verocay body arranged in a palisading pattern with compact areas of spindle cells, representing the Antoni A area, alongside loosely arranged hypocellular foci in the Antoni B area (hematoxylin & eosin stain, ×100). B: Immunohistochemical staining yielded a strongly positive reaction for S-100 protein, a useful marker for schwannoma (S-100 stain, ×100).

  • Fig. 5. Postoperative magnetic resonance T1-weighted image showing no evidence of recurrence in the area of the vidian canal, with associated mucosal swelling.


Reference

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