4.2 Article

Key Genes and Endoscopic Radical Surgery in Primary Middle Ear Oncocytic Papillomas

Journal

OTOLOGY & NEUROTOLOGY
Volume 44, Issue 9, Pages E676-E680

Publisher

LIPPINCOTT WILLIAMS & WILKINS
DOI: 10.1097/MAO.0000000000003993

Keywords

Endoscopic surgery; Gene expression; Middle ear; Oncocytic papilloma

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Middle ear oncocytic papillomas are extremely rare and not fully understood. The use of RNA sequencing analysis can provide better understanding and management of middle ear papillomas.
ObjectivePapillomas originating from the Schneiderian epithelium within the middle ear are extremely rare and may be associated with a high rate of recurrence and malignant transformation. Oncocytic papillomas represent the rarest pathological subtype of such tumors. The current investigation aimed to determine whether there exists a distinct mechanism underlying the incidence of oncocytic papillomas arising primarily within the middle ear, and to explore potential treatment strategies to ensure complete removal and prevent recurrence.Study DesignSearch of the English literature for cases of middle ear papilloma and RNA sequencing analysis of three samples from one new case presenting at the Eye and ENT Hospital, Fudan University (Shanghai, China), with recurrent middle ear oncocytic papilloma, along with two normal mucosal samples.SettingAcademic, tertiary referral hospital.Patient and interventionsThe patient underwent open mastoidectomy and endoscopic tympanoplasty twice in 6 years. Histopathology confirmed oncocytic papilloma in middle ear. The patient has been free of the disease at 18 months of follow-up without radiation, whereas the RNA-seq analysis of the samples in endoscopic operations remained nonmalignant.ResultsOnly four cases of primary middle ear oncocytic papillomas have been reported. Recurrent masses usually originate from around the eustachian tube, which may explain the pathogenesis of this lesion. RNA-seq analysis was used to identify 1,317 (UP, 239; DOWN, 1078) differentially expressed genes between papillomas and normal mucosa. The involvement of some hub proteins (e.g., FN1, CXCL8, L10, JUN, and FOS) in the pathogenesis of primary middle ear papillomas was found to align with the observed clinical features.ConclusionThe middle ear oncocytic papillomas were extremely rare and remained incompletely understood. The findings of this first RNA-seq analysis of this rare tumor may serve to enhance comprehension of and aid in the management of middle ear papillomas.

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