Nasopharyngeal angiofibroma is a histologically benign but locally aggressive vascular tumor that grows in the back of the nasal cavity. It most commonly affects adolescent males and may grow into fissures of the. Nasoangiofibroma youth is a highly vascularized tumor almost exclusively male adolescents presentation. % represents % of head and. Angiofibroma nasofaring juvenile – Free download as PDF File .pdf), Text File . txt) or read online for free.
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They account for only 0. The presentation is typically with obstructive symptoms, epistaxisand chronic otomastoiditis due to obstruction of the Eustachian tube. Patients may present with life-threatening epistaxis.
Juvenile nasopharyngeal angiofibroma
On examination, it may be seen as a pale reddish-blue mass. It is, as the name suggests, very angiofirboma and a biopsy can sometimes be fatal. Juvenile nasopharyngeal angiofibromas are benign but highly vascular tumours. They may be locally aggressive.
Pathology Outlines – Nasopharyngeal angiofibroma
The exact site of origin angioibroma contentious as these masses usually present when they have reached considerable size. However, most authors agree that JNAs arise from the posterior choanal tissues in the region of the sphenopalatine foramen. See staging of juvenile nasopharyngeal angiofibromas. Imaging plays an important role in diagnosis, as biopsies should be avoided due muvenile the risk of brisk hemorrhage, as well as staging.
Although these masses are thought to arise from the region of the sphenopalatine foramenthey are usually sizeable at diagnosis, frequently with extension medially into the nasopharynxlaterally into the pterygopalatine fossa and over time beyond, into the orbitparanasal sinusesintracranial cavity and infratemporal fossa.
Plain radiographs no longer play a role in the workup of a suspected juvenile nasopharyngeal angiofibroma, however they may still be obtained in some instances during the assessment of nasal obstruction, or symptoms of sinus obstructions.
CT is particularly useful at delineating juveinle changes. Findings are similar to those described above.
Typically a lobulated non-encapsulated soft tissue mass is demonstrated centred on the sphenopalatine foramen which is often widened and usually bowing the posterior wall juvvenile the maxillary antrum anteriorly. There is marked contrast enhancement following administration of juvneile, reflecting the prominent vascularity. Extensive bony destruction is usually not a feature, but rather bone is remodelled or resorbed. This feature may be helpful is differentiating from other more aggressive lesions.
Intracranial extension can however occur. Angiography, although not essential, is often useful in both defining the feeding vessels as well as in preoperative embolisation. Supply of these tumours is usually via The presence of prominent jjuvenile voids lead to a salt and pepper appearance on most sequences and are characteristic 5,6. Surgical resection either open or increasingly endoscopic is the treatment of choice, usually performed with nasfoaring embolisation to help with haemostasis.
Irradiation may be an option if surgery is not possible or only incomplete resection achieved 2,4,6. You can also scroll through stacks with your mouse wheel or the keyboard arrow keys. Unable to process the form. Check for errors and try again. Thank you for updating your details.
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