Bilateral Blindness in a Patient With Vestibular Schwannoma and Empty Sella Syndrome: A Case Report

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Authors: Ammar M Bahati, Thamer H Alsharif, Mashhour A Alsuwat, Kemal Dizdarević
Cited by: 0
References: 7

Abstract

We report a rare clinical presentation of a T4b vestibular schwannoma causing severe compression of the brainstem and fourth ventricle, associated with obstructive hydrocephalus and empty sella syndrome, in a patient presenting with profound neurological and ophthalmological deficits, most notably complete bilateral blindness. Radical microsurgical resection was achieved via a lateral suboccipital (retromastoid) approach, resulting in gross-total tumor removal with preservation of most cranial nerves. Postoperatively, the patient developed House-Brackmann grade III facial palsy. Hydrocephalus resolved without the need for cerebrospinal fluid diversion, gait instability improved, and visual deficits persisted. This case highlights the exceptional association of vestibular schwannoma with bilateral blindness and empty sella syndrome, emphasizing the importance of early recognition and timely surgical intervention in advanced tumors to minimize morbidity and optimize outcomes.

Fields of Study & Subjects

Meningioma and schwannoma management Pituitary Gland Disorders and Treatments Neurofibromatosis and Schwannoma Cases

Publication details

Journal / source
Cureus
Volume
18
Issue
1
Pages
e101505–e101505
Publication date
14 January 2026
Language
EN