Juvenile angiofibroma is a rare, benign and highly vascular tumor that develops almost exclusively in adolescent males within the sphenopalatine foramen. It presents with recurrent severe nosebleeds and progressive nasal obstruction. Imaging such as CT and MRI are used to determine the extent of the tumor. While surgery is the primary treatment, preoperative embolization and endoscopic resection are often used for early-stage tumors to reduce bleeding and complications. Advanced tumors may require open approaches like mid-facial degloving. Recurrence rates remain high due to the invasive nature of the tumor.