Giant cerebellopontine angle schwannoma in a child.

To cite: Gabel BC, Newbury RO, Levy ML, et al. BMJ Case Rep Published online: [please include Day Month Year] doi:10.1136/ bcr-2013-201253 DESCRIPTION A 6-year-old boy presented with a 6-month history of worsening gait, abnormal eye movements and head tilt. Neurological examination revealed papilloedema, gaze-evoked nystagmus, decreased rightsided hearing, decreased sensation in the right V1 trigeminal nerve distribution, bilateral dysmetria and ataxic gait. MRI demonstrated a large contrast-enhancing, right-sided cerebellopontine angle tumour with mass effect on the fourth ventricle and invasion of the cavernous sinus (figure 1). T2-weighted MRI sequences showed enlargement of optic nerve sheaths and protrusion of optic nerve heads consistent with increased intracranial pressure (figure 1C). Subtotal resection of the mass consisted of a spindle cell neoplasm with palisading nuclei forming Verocay bodies, and both Antoni A and B patterns, consistent with a diagnosis of schwannomas (figure 2). Postoperatively he required prolonged rehabilitation due to complications from surgery including right-sided cranial neuropathy and left hemiparesis that resolved over several weeks. Owing to residual disease in the brainstem and cavernous sinus, the patient underwent conformal intensity modulated radiation therapy and remained stable for almost 3 years postdiagnosis. Genetic testing for neurofibromatosis types 1 and 2 was negative and the child had no neurocutaneous findings. Schwannomas of the cerebellopontine angle are uncommon in the absence of acoustic nerve involvement. There have been a limited number of case reports of spontaneous intracranial schwannomas in children. 2 Up to 40% of children with cerebellopontine angle tumours may be negative for neurofibromatosis type 2. Our case expands the differential diagnosis of cerebellopontine angle