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Vagal Paraganglioma and Schwannoma—Surgical or Non-surgical Management

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Book cover Difficult Decisions in Head and Neck Oncologic Surgery

Abstract

Vagal paragangliomas and schwannomas have traditionally been treated by surgical excision. Surgery is however associated with very high rates of permanent Vagal paralysis, and alternate treatments have therefore been explored for patients with preserved vagal nerve function.

Vagal paragangliomas that are minimally symptomatic with preserved nerve function, or in the elderly or high surgical risk patient, may be suitably managed by periodic MR scanning to ascertain for manifest growth prior to initiating treatment. Surgery and its morbidity may therefore be temporarily or permanently deferred, though tumor growth and new cranial nerve palsies are reported in 55% over a 4 year median follow up. Concerns also exist regarding the potential for associated malignancy. Fractionated Radiation is effective in preventing tumor growth but concerns exist of breakout growth in the long term. Surgery when undertaken should be accompanied by thyroplasty and rehabilitative procedures to minimize the morbidity of vagal paralysis.

Patients should be involved in formulating an individualized treatment plan. Genetic testing may help in prognostication and treatment selection and its value is likely to increase in the future.

Non-surgical treatments for Schwannoma in the nature or watchful waiting and stereotactic radiation are not yet fully tested but are promising alternatives.

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Sakthivel, P., Mittal, P., Thakar, A. (2019). Vagal Paraganglioma and Schwannoma—Surgical or Non-surgical Management. In: Gooi, Z., Agrawal, N. (eds) Difficult Decisions in Head and Neck Oncologic Surgery. Difficult Decisions in Surgery: An Evidence-Based Approach. Springer, Cham. https://doi.org/10.1007/978-3-030-15123-2_17

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