Case report highlights the rarity of neuroendocrine tumors in the middle ear, suggesting a unique surgical approach for treatment.
Neuroendocrine tumors originating in the middle ear are rare, and presentation with facial paralysis is extremely uncommon. A 19-year-old woman with a history of transient facial paralysis presented with a right-sided middle ear mass. Surgical exploration of the tympanic cavity was performed using a transcanal endoscopic approach. Histopathologic examination confirmed the diagnosis of a middle ear neuroendocrine tumor. After surgical excision of the tumor, no recurrence or facial paralysis occurred. Herein, the authors present this rare case, along with a literature review.
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Shin et al. (2025) studied this question.
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