Juvenile nasopharyngeal angiofibroma

Juvenile nasopharyngeal angiofibroma (JNA) is a rare and benign but locally aggressive fibrovascular tumor arising from the posterolateral wall of the nasopharynx, which affects mainly young and adolescent males (onset usually occurring between 7-19 years of age) and that presents as a mass in the nasopharynx and nasal cavity, leading to manifestations such as nasal obstruction, epistaxis, profound facial swelling, proptosis or diplopia. Although slowly progressive, it has a high rate of recurrence and sometimes invades adjacent structures.

Also known as: JNA, juvenile nasopharyngeal angiofibroma, juvenile nasopharyngeal angiofibroma (disease), nasopharyngeal angiofibroma, nasopharyngeal juvenile angiofibroma

1439 clinical trials for this condition and its sub-types, 1 tagged with Juvenile nasopharyngeal angiofibroma itself.