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Juvenile Nasopharyngeal Angiofibroma (JNA)

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Atlas of Sellar and Parasellar Lesions

Abstract

Juvenile nasopharyngeal angiofibroma (JNA) is a rare, histologically benign skull base tumor that develops in adolescents and young adults, almost exclusively in males.

JNAs represent less than 1 % of head and neck tumors.

The median age at diagnosis is 15 years.

The incidence rate of JNA is 0.4 per million persons per year and as high as 3.7 per million males per year.

Patients typically present with epistaxis and nasal obstruction.

JNA may be related to familial adenomatous polyposis (FAP).

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Correspondence to Gabriel Zada MD, MS .

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Zada, G., Lopes, M.B.S., Mukundan, S., Laws, E. (2016). Juvenile Nasopharyngeal Angiofibroma (JNA). In: Zada, G., Lopes, M., Mukundan Jr., S., Laws Jr., E. (eds) Atlas of Sellar and Parasellar Lesions. Springer, Cham. https://doi.org/10.1007/978-3-319-22855-6_49

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  • DOI: https://doi.org/10.1007/978-3-319-22855-6_49

  • Publisher Name: Springer, Cham

  • Print ISBN: 978-3-319-22854-9

  • Online ISBN: 978-3-319-22855-6

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