Vestibular schwannoma: role of conservative management

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Vestibular schwannoma: role of conservative management.

OBJECTIVE To assess the outcome of conservative management of vestibular schwannoma. STUDY DESIGN Observational study. SETTING Tertiary referral centre. PATIENTS Four hundred and thirty-six patients with vestibular schwannoma (490 tumours), including 327 sporadic tumours and 163 tumours in 109 patients with neurofibromatosis type two. MAIN OUTCOME MEASURES The relationship of tumour gro...

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Conservative management of vestibular schwannoma.

INTRODUCTION Vestibular schwannoma (VS) is a benign, slow-growing tumour originating in the 8th cranial nerve. The treatment includes microsurgery, stereotactic radiotherapy and conservative management of tumours with periodic radiological tests. METHODS This was a retrospective study of patients with VS following conservative management in a tertiary hospital between 1993 and 2013. A total o...

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Conservative management of vestibular schwannoma: Predictors of growth and hearing.

OBJECTIVE To describe the clinical outcomes of patients undergoing serial observation for vestibular schwannoma (VS) and identify factors that may predict tumor growth or hearing loss. STUDY DESIGN Retrospective review. METHODS A retrospective review was conducted of patients seen at a tertiary care medical center between 2002 and 2013 with an International Classification of Diseases-9 diag...

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Vestibular Function In Vestibular Schwannoma

Introduction: Traditionally vestibular function has been assessed using caloric irrigations; new methods have failed to reach the same level of accuracy. Vestibular nerve dysfunction occurs with 'acoustic neuroma' or 'vestibular schwannoma. Quantitative testing of hearing by audiometry is much more widely available than quantitative vestibular testing, although consideration of vestibular dysfu...

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Diagnosis and Management of Hereditary Meningioma and Vestibular Schwannoma.

Bilateral vestibular schwannomata and meningiomata are the tumours most commonly associated with neurofibromatosis type II (NF2). These tumours may also be seen in patients with schwannomatosis and familial meningioma, but these phenotypes are usually easy to distinguish. The main diagnostic challenge when managing these tumours is distinguishing between sporadic disease which carries low risk ...

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ژورنال

عنوان ژورنال: The Journal of Laryngology & Otology

سال: 2009

ISSN: 0022-2151,1748-5460

DOI: 10.1017/s0022215109992362