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- W2023932275 abstract "Objective: 1) Review anatomy of the nasolacrimal apparatus. 2) Learn about common primary tumors of the nasolacrimal apparatus and their clinical presentation. 3) Present a rare type of nasolacrimal duct tumor. 4) Discuss the utility of combined endoscopic and external techniques for removal of nasolacrimal duct tumors.Method: Retrospective case report and review of literature.Results: A 67-year-old woman presented with cough and post-nasal drip. Examination revealed a right-sided nasal cavity mass anterior to the middle turbinate. Upon further questioning, she reported a history of right nasal dorsal pain, but denied epiphora, epistaxis, and ocular symptoms. Imaging revealed a mass originating from the right nasolacrimal duct with extension into the right peri-orbital soft tissues. The tumor was completely excised via combined endoscopic and external approaches. Histopathologic examination identified the lesion as Warthin tumor. At 1 year postoperatively, the patient is disease- and symptom-free.Conclusion: Primary tumors of the nasolacrimal apparatus are rare. These tumors must be in the differential diagnosis of a patient presenting with nasal obstruction, epiphora, and nasal-cavity mass. It is important for otolaryngologists to be familiar with the different pathologies that involve the nasolacrimal apparatus and their clinical presentation." @default.
- W2023932275 created "2016-06-24" @default.
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- W2023932275 date "2011-08-01" @default.
- W2023932275 modified "2023-10-13" @default.
- W2023932275 title "Warthin Tumor of Nasolacrimal Duct" @default.
- W2023932275 doi "https://doi.org/10.1177/0194599811415823a82" @default.
- W2023932275 hasPublicationYear "2011" @default.
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