Diagnosis and management of pediatric cervical vagal schwannoma

Publication date: Available online 23 August 2018

Source: International Journal of Pediatric Otorhinolaryngology

Author(s): Józef Mierzwiński, Iwona Wrukowska, Justyna Tyra, Dariusz Paczkowski, Tomasz Szcześniak, Karolina Haber

Abstract

Schwannomas arising from the vagus nerve are extremely rare in children, with only 15 cases reported in the world literature.

We describe a pediatric case of cervical vagal nerve schwannoma successfully treated with cranial nerve-sparing surgery. Our patient presented extensive mass in the right side of the neck with ipsilateral Horner's syndrome. Her first sign, anisocoria, was diagnosed at the age of 1.5 y, making her the youngest vagal schwannoma case ever reported. Using an ultrasonic surgical aspirator and nerve monitoring, a multidisciplinary team successfully removed the mass with no recurrence after 2 years of follow-up.

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