Juvenile angiofibroma is a noncancerous growth of the back of the nose or upper throat.
Nasal tumor; Angiofibroma - juvenile; Benign nasal tumor; Juvenile nasal angiofibroma; JNA
Causes, incidence, and risk factors
Juvenile angiofibroma is not very common. It is usually found in adolescent boys. The
Difficulty breathingthrough the nose
- Easy bruising
- Frequent or repeated nosebleeds
Hearing loss Nasal discharge, usually bloody
- Stuffy nose
Signs and tests
The doctor may see the angiofibroma when examining the upper throat.
Tests that may be done include:
Arteriogramto see the blood supply to the growth CT scan of the head
- MRI scan of the head
Biopsy is generally not recommended due to the high risk of bleeding.
You will need treatment if the angiofibroma is growing larger, blocking the airways, or causing repeated nosebleeds. In some cases, no treatment is needed.
Surgery may be needed to remove the tumor. The tumor may be hard to remove if it is not enclosed and has spread to other areas. Newer surgery techniques that place a camera up through the nose have made tumor removal surgery less invasive.
A procedure called embolization may be done to prevent the tumor from bleeding. The procedure may correct the nosebleeds by itself, but it is usually followed by surgery to remove the tumor.
Although not cancerous, angiofibromas may continue to grow. Some may disappear on their own.
It is common for the tumor to return after surgery.
- Pressure on the brain (rare)
- Spread of the tumor to the nose, sinuses, and other structures
Calling your health care provider
Call your health care provider if you often have nosebleeds.
There is no known way to prevent this condition.
Nicolai P, Castelnuovo P. Benign tumors of the sinonasal tract. In: Flint PW, Haughey BH, Lund LJ, et al, eds. Cummings Otolaryngology: Head & Neck Surgery. 5th ed. Philadelphia, Pa: Mosby Elsevier; 2010:chap 49.
Haddad J Jr. Epistaxis. In: Kliegman RM, Behrman RE, Jenson HB, Stanton BF, eds. Nelson Textbook of Pediatrics. 19th ed. Philadelphia, Pa: Saunders Elsevier; 2011:chap 369.2.