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Scholars Journal of Medical Case Reports | Volume-9 | Issue-06
Paragangliomas of Nasal Cavity: A Case Report
Niema Benkhraba, Mohamed Ali Gliti, Ihssane Allouch, Sophia Nitassi, Bencheikh Razika, Benbouzid Mohamed Anas, Abdelilah Oujilal, Leila Essakalli Houssyni
Published: June 22, 2021 | 206 171
DOI: 10.36347/sjmcr.2021.v09i06.015
Pages: 673-675
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Abstract
Paraganglioma is a rare neuroendocrine tumor. Nasal localization is very rare. Head and neck paragangliomas represent only 0.6% of head and neck tumors and 3% of all paragangliomas. The treatment is based on surgery. Radiotherapy is indicated if the surgery does not provide complete resection. We report the case of a 36-year-old patient who has had left nasal obstruction with epistaxis for 2 years. The CT scan shows a solid mass centered on the left nasal cavity, puffy, without signs of aggression, benign-looking. The patient underwent a complete endoscopic endonasal tumor removal after preoperative external carotid embolization. Pathological analysis with immunohistochemistry confirmed the diagnosis of paraganglioma. The follow-up to the treatment was favorable.