Temporal Bone Adenoma: A Comprehensive Analysis of Clinical Aspects and Surgical Outcome on a Very Rare Entity

Author:

Alsalman Hussain12,Crowther John A.1,McLellan Douglas3,Kontorinis Georgios1

Affiliation:

1. Department of Otorhinolaryngology, Queen Elizabeth University Hospital, Glasgow, United Kingdom

2. Medical School, King Saud University, Riyadh, Saudi Arabia

3. Department of Pathology, Queen Elizabeth University Hospital, Glasgow, United Kingdom

Abstract

Abstract Objective The aim of this study is to present our experience in dealing with middle ear adenomas (MEAs), very rare tumors of the middle ear. Methods The medical notes of individuals with MEAs treated in tertiary referral; academic settings were retrospectively reviewed. We recorded the presenting symptoms, imaging findings, and pathology results. We additionally examined our surgical outcomes, follow-up period, recurrence, and morbidity. Results We identified four patients with MEAs: two males and two females with an average age of 36.25 years (range = 27–51 years). Despite the detailed imaging studies, including computed tomography and magnetic resonance imaging with intravenous contrast administration, a biopsy was essential in setting the diagnosis. Total surgical resection was achieved in all patients without any recurrence over an average of 6 years (range = 3–10 years). Complete ipsilateral deafness was the commonest surgical morbidity due to footplate infiltration by the tumor. Conclusion Total surgical resection is the treatment of choice in MEAs to minimize the risk for recurrence; this can come with morbidity, mostly sensorineural deafness. Given the very limited literature, long-term follow-up is recommended.

Publisher

Georg Thieme Verlag KG

Subject

Clinical Neurology

Reference8 articles.

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3. Neuroendocrine adenoma of the middle ear confused with congenital cholesteatoma;Y H Kim;Rev Bras Otorrinolaringol (Engl Ed),2014

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5. Middle ear adenoma: case report and discussion;D Isenring;Case Rep Otolaryngol,2014

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